- A.FeO
- B.Fe2O3
- C.Fe3O4
- D.Fe3O2
Edexcel IAL · Thinka 原創模擬試題
2025 Edexcel IAL Chemistry (YCH11) 模擬試題連答案詳解
Thinka Oct 2025 (V2) Cambridge International A Level-Style Mock — Chemistry (YCH11)
WCH11 甲部
- A.9.72 x 10^-6 mol
- B.9.72 x 10^-3 mol
- C.1.08 x 10^-2 mol
- D.1.08 x 10^1 mol
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解題
評分準則
- A.24.00
- B.24.30
- C.24.32
- D.25.00
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解題
評分準則
- A.1s2 2s2 2p6 3s2 3p6 3d3
- B.1s2 2s2 2p6 3s2 3p6 4s1 3d2
- C.1s2 2s2 2p6 3s2 3p6 4s2 3d1
- D.1s2 2s2 2p6 3s2 3p6 3d5
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解題
評分準則
- A.Trigonal planar, 120 degrees
- B.Trigonal pyramidal, 107 degrees
- C.Tetrahedral, 109.5 degrees
- D.T-shaped, 90 degrees
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解題
評分準則
- A.W: Simple molecular covalent; X: Giant covalent; Y: Giant metallic; Z: Giant ionic
- B.W: Simple molecular covalent; X: Giant ionic; Y: Giant metallic; Z: Giant covalent
- C.W: Giant ionic; X: Simple molecular covalent; Y: Giant metallic; Z: Giant covalent
- D.W: Simple molecular covalent; X: Giant ionic; Y: Giant covalent; Z: Giant metallic
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解題
評分準則
- A.Cl2 -> 2Cl.
- B.CH3. + Cl. -> CH3Cl
- C.CH4 + Cl. -> CH3. + HCl
- D.CH3. + CH3. -> C2H6
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解題
評分準則
- A.2-bromo-2-methylbutane
- B.2-bromo-3-methylbutane
- C.1-bromo-2-methylbutane
- D.1-bromo-3-methylbutane
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解題
評分準則
Which of the following could be the molecular formula of this compound?
[Molar volume of gas at rtp = 24.0 dm\(^3\) mol\(^{-1}\)]
- A.C\(_3\)H\(_6\)O
- B.C\(_3\)H\(_8\)O
- C.C\(_2\)H\(_6\)O
- D.C\(_3\)H\(_6\)O\(_2\)
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解題
\(n(\text{O}_2) = \frac{14.4 \text{ dm}^3}{24.0 \text{ dm}^3 \text{ mol}^{-1}} = 0.600 \text{ mol}\).
Now find the molar ratio of the organic compound to oxygen:
\(\frac{n(\text{O}_2)}{n(\text{compound})} = \frac{0.600}{0.150} = 4.0\).
So, 1 mole of the compound requires exactly 4 moles of \(\text{O}_2\) for complete combustion.
Let's test the given options by writing balanced combustion equations:
- For C\(_3\)H\(_6\)O:
\(\text{C}_3\text{H}_6\text{O} + 4\text{O}_2 \rightarrow 3\text{CO}_2 + 3\text{H}_2\text{O}\) (Balanced: oxygen atoms on right = 6 + 3 = 9; left = 1 + 8 = 9. Correct!)
- For C\(_3\)H\(_8\)O:
\(\text{C}_3\text{H}_8\text{O} + 4.5\text{O}_2 \rightarrow 3\text{CO}_2 + 4\text{H}_2\text{O}\) (Incorrect)
- For C\(_2\)H\(_6\)O:
\(\text{C}_2\text{H}_6\text{O} + 3\text{O}_2 \rightarrow 2\text{CO}_2 + 3\text{H}_2\text{O}\) (Incorrect)
- For C\(_3\)H\(_6\)O\(_2\):
\(\text{C}_3\text{H}_6\text{O}_2 + 3.5\text{O}_2 \rightarrow 3\text{CO}_2 + 3\text{H}_2\text{O}\) (Incorrect)
評分準則
$$\begin{array}{|c|c|c|c|c|c|} \hline \text{1st} & \text{2nd} & \text{3rd} & \text{4th} & \text{5th} & \text{6th} \\ \hline 578 & 1817 & 2745 & 11578 & 14831 & 18378 \\ \hline \end{array}$$
Which of the following statements about element X is correct?
- A.Element X forms an ionic chloride with the formula XCl\(_2\).
- B.Element X has a higher first ionisation energy than the element immediately to its left in Period 3.
- C.Element X has the lowest melting point in Period 3.
- D.The oxide of element X is amphoteric.
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解題
In Period 3, this element is aluminium (Al).
- Al forms the chloride \(\text{AlCl}_3\) (or \(\text{Al}_2\text{Cl}_6\)), which has covalent character, so (a) is incorrect.
- Al is to the right of magnesium (Mg) in Period 3. Mg (\([\text{Ne}]3s^2\)) has a higher first ionisation energy than Al (\([\text{Ne}]3s^2 3p^1\)) because the electron removed from Al is in a higher-energy 3p orbital and is shielded by the 3s electrons, so (b) is incorrect.
- Al has a relatively high melting point due to metallic bonding, so (c) is incorrect.
- Aluminium oxide (\(\text{Al}_2\text{O}_3\)) is amphoteric as it reacts with both acids and bases, making (d) correct.
評分準則
- A.PH\(_3\)
- B.SO\(_2\)
- C.H\(_3\)O\(^+\)
- D.NH\(_4\)\(^+\)
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解題
- SO\(_2\) has a central sulfur atom with 2 bonding regions (double/coordinate bonds) and 1 lone pair. This gives a bent shape based on a trigonal planar electron geometry. The repulsion from the lone pair reduces the bond angle from 120\(^\circ\) to approximately 119\(^\circ\), which is closest to 120\(^\circ\).
- H\(_3\)O\(^+\) has 3 bonding pairs and 1 lone pair, giving a trigonal pyramidal shape with a bond angle of about 107\(^\circ\).
- NH\(_4\)\(^+\) is tetrahedral with a bond angle of 109.5\(^\circ\).
評分準則
Which of the following represents a propagation step in this reaction?
- A.Br\(_2 \rightarrow\) 2Br\(^\bullet\)
- B.C\(_3\)H\(_7\)\(^\bullet\) + Br\(^\bullet \rightarrow\) C\(_3\)H\(_7\)Br
- C.C\(_3\)H\(_8\) + Br\(^\bullet \rightarrow\) C\(_3\)H\(_7\)\(^\bullet\) + HBr
- D.C\(_3\)H\(_8\) + Br\(^\bullet \rightarrow\) C\(_3\)H\(_7\)Br + H\(^\bullet\)
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解題
- Option b is a termination step (combination of two free radicals).
- Option c is a propagation step where a bromine radical abstracts a hydrogen atom from propane to form a propyl radical and hydrogen bromide.
- Option d is incorrect because free hydrogen radicals (H\(^\bullet\)) are not produced during these radical reactions.
評分準則
Which of the following statements correctly explains why 2-bromopropane is the major product?
- A.The 2-bromopropane is formed via a secondary carbocation, which is more stable than the primary carbocation due to the positive inductive effect of two alkyl groups.
- B.The 2-bromopropane is formed via a primary carbocation, which is more stable than the secondary carbocation because it has less steric hindrance.
- C.Bromine is a more electronegative atom and prefers to attack the secondary carbon atom directly.
- D.Hydrogen bromide acts as a nucleophile, attacking the carbon atom with fewer hydrogen atoms.
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解題
評分準則
What is the relative molecular mass (\(M_r\)) of the volatile liquid?
[Gas constant, R = 8.31 J mol\(^{-1}\) K\(^{-1}\)]
- A.30.8
- B.82.5
- C.115.0
- D.244.4
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解題
First, convert all units to SI units:
- Pressure, \(p = 101 \text{ kPa} = 101,000 \text{ Pa}\)
- Volume, \(V = 75.0 \text{ cm}^3 = 75.0 \times 10^{-6} \text{ m}^3\)
- Temperature, \(T = 100 ^\circ\text{C} = 100 + 273 = 373 \text{ K}\)
Now, calculate the number of moles of gas, \(n\):
\(n = \frac{pV}{RT} = \frac{101,000 \times 75.0 \times 10^{-6}}{8.31 \times 373} = \frac{7.575}{3099.63} \approx 0.002444 \text{ mol}\)
Finally, calculate the relative molecular mass (\(M_r\)):
\(M_r = \frac{\text{mass}}{n} = \frac{0.281}{0.002444} \approx 115.0\)
- Option a is obtained if temperature is incorrectly left in \(^\circ\)C (100 K instead of 373 K).
評分準則
- A.[Ar] 3d\(^9\)
- B.[Ar] 4s\(^2\) 3d\(^7\)
- C.[Ar] 4s\(^1\) 3d\(^8\)
- D.[Ar] 3d\(^{10}\)
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解題
When transition metals form cations, they lose electrons from the outermost s-subshell (4s) before losing electrons from the d-subshell (3d).
To form \(\text{Cu}^{2+}\), we remove 2 electrons:
1. First electron is removed from the 4s orbital, leaving \([\text{Ar}] 3d^{10}\).
2. Second electron is removed from the 3d orbital, leaving \([\text{Ar}] 3d^9\).
評分準則
- A.C–F
- B.N–F
- C.O–F
- D.F–F
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解題
Fluorine is the most electronegative element with a value of 4.0. The electronegativity values of the other Period 2 elements are approximately:
- Carbon (C): 2.5
- Nitrogen (N): 3.0
- Oxygen (O): 3.5
The electronegativity differences for the bonds are:
- C–F: \(4.0 - 2.5 = 1.5\)
- N–F: \(4.0 - 3.0 = 1.0\)
- O–F: \(4.0 - 3.5 = 0.5\)
- F–F: \(4.0 - 4.0 = 0.0\)
The C–F bond has the largest electronegativity difference, making it the most polar single bond among the choices.
評分準則
- A.0.0647
- B.6.47
- C.64.7
- D.647
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解題
評分準則
- A.\(XO_2\)
- B.\(X_2O_3\)
- C.\(X_2O_5\)
- D.\(XO_3\)
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解題
評分準則
- A.\(H_2O\)
- B.\(NH_3\)
- C.\(BF_3\)
- D.\(CH_4\)
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解題
評分準則
- A.but-1-ene
- B.but-2-ene
- C.2-methylbut-2-ene
- D.pent-2-ene
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解題
評分準則
WCH11 乙部
(a) Write the equation for the complete thermal decomposition of anhydrous basic copper carbonate, \(\text{Cu}_2\text{CO}_3\text{(OH)}_2\). Include state symbols. [2 marks]
(b) A student performed the decomposition of the hydrated salt using a crucible.
- Mass of empty crucible = \(14.650\text{ g}\)
- Mass of crucible + hydrated salt = \(18.235\text{ g}\)
- Mass of crucible + residue (CuO) after heating to constant mass = \(17.035\text{ g}\)
(i) Calculate the mass of the CuO residue formed and the mass of the volatile gases (\(\text{CO}_2\) and \(\text{H}_2\text{O}\)) lost. [2 marks]
(ii) Calculate the amount, in moles, of CuO residue formed. [2 marks]
(iii) Use the stoichiometry of the decomposition reaction to show that \(0.0150\text{ mol}\) of \(\text{CO}_2\) is released, and calculate its mass. [2 marks]
(iv) Calculate the mass and amount, in moles, of water lost, and hence determine the value of \(x\) in the formula. Show your working. [4 marks]
(c) State two assumptions or potential sources of error in this experiment and explain how they could affect the calculated value of \(x\). [3 marks]
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解題
(b)(i) Mass of CuO residue = \(17.035 - 14.650 = 2.385\text{ g}\).
Mass of volatile gases lost = \(18.235 - 17.035 = 1.200\text{ g}\).
(b)(ii) Molar mass of CuO = \(63.5 + 16.0 = 79.5\text{ g mol}^{-1}\).
Moles of CuO = \(2.385 / 79.5 = 0.0300\text{ mol}\).
(b)(iii) From the equation, 2 moles of CuO are produced for every 1 mole of \(\text{CO}_2\). Therefore, moles of \(\text{CO}_2\) = \(0.0300 / 2 = 0.0150\text{ mol}\).
Mass of \(\text{CO}_2\) = \(0.0150 \times 44.0 = 0.660\text{ g}\).
(b)(iv) Mass of water lost = Total volatile mass - Mass of \(\text{CO}_2\) = \(1.200 - 0.660 = 0.540\text{ g}\).
Moles of water lost = \(0.540 / 18.0 = 0.0300\text{ mol}\).
Total water lost includes the water from the hydroxide group plus the water of crystallization.
From stoichiometry, 1 mole of hydrated basic copper carbonate containing 1 mole of \(\text{Cu(OH)}_2\) yields 1 mole of water of constitution.
Since moles of basic copper carbonate is equal to moles of \(\text{CO}_2 = 0.0150\text{ mol}\), the moles of water from the decomposition of the hydroxide group is \(0.0150\text{ mol}\).
Moles of water of crystallization = \(0.0300 - 0.0150 = 0.0150\text{ mol}\).
Ratio of water of crystallization to basic copper carbonate = \(0.0150 / 0.0150 = 1\).
Therefore, \(x = 1\).
(c) Potential sources of error:
1. Incomplete decomposition (not heated to constant mass), which leaves some carbonate undecomposed, leading to an underestimate of mass lost and therefore a lower value of \(x\).
2. Loss of solid residue due to spitting during heating, which increases the apparent mass lost, leading to an overestimate of water lost and therefore a higher value of \(x\).
評分準則
- M1: Correct reactants and products: \(\text{Cu}_2\text{CO}_3\text{(OH)}_2 \to 2\text{CuO} + \text{CO}_2 + \text{H}_2\text{O}\) (1)
- M2: Correct state symbols: (s) for reactant and residue, (g) for \(\text{CO}_2\) and \(\text{H}_2\text{O}\) (1)
(b)(i)
- M1: Mass of CuO residue = 2.385 g (1)
- M2: Mass of volatiles lost = 1.200 g (1)
(b)(ii)
- M1: Calculation of molar mass of CuO = 79.5 (1)
- M2: Moles of CuO = 0.0300 mol (1)
(b)(iii)
- M1: Deducing moles of \(\text{CO}_2 = 0.0150\text{ mol}\) by halving the moles of CuO (1)
- M2: Mass of \(\text{CO}_2\) = 0.660 g (1)
(b)(iv)
- M1: Mass of water lost = 0.540 g (1)
- M2: Moles of water lost = 0.0300 mol (1)
- M3: Deducing moles of water of crystallization = 0.0150 mol (1)
- M4: Dividing by moles of salt (0.0150 mol) to get \(x = 1\) (1)
(c)
- M1: Identified error 1 (e.g., incomplete decomposition) and its effect (underestimates mass lost / underestimates \(x\)) (1)
- M2: Identified error 2 (e.g., loss of solid by spitting) and its effect (overestimates mass lost / overestimates \(x\)) (1)
- M3: Suggestion to minimize (e.g., heat to constant mass or use a lid on the crucible) (1)
(a) A sample of element M was analyzed in a mass spectrometer. The sample was found to contain two isotopes:
- Isotope 1: mass = 69.0 with abundance = 60.1%
- Isotope 2: mass = 71.0 with abundance = 39.9%
Calculate the relative atomic mass of M to two decimal places and identify element M. [3 marks]
(b) Describe how these isotopes are accelerated, how they are detected in a time-of-flight (TOF) mass spectrometer, and how their abundance is measured. [4 marks]
(c) The successive ionization energies of element Z, which is in Period 3, are given below:
- 1st IE: \(1012\text{ kJ mol}^{-1}\)
- 2nd IE: \(1903\text{ kJ mol}^{-1}\)
- 3rd IE: \(2912\text{ kJ mol}^{-1}\)
- 4th IE: \(4956\text{ kJ mol}^{-1}\)
- 5th IE: \(6273\text{ kJ mol}^{-1}\)
- 6th IE: \(21268\text{ kJ mol}^{-1}\)
- 7th IE: \(25431\text{ kJ mol}^{-1}\)
(i) Identify the group to which Z belongs, giving a reason based on the data. [2 marks]
(ii) Write the equation, including state symbols, for the reaction corresponding to the third ionization energy of element Z. [2 marks]
(d) Write the full electronic configuration of:
(i) the neutral atom of Z. [1 mark]
(ii) the stable ion of Z formed when it reacts with calcium. [1 mark]
(e) Explain why the first ionization energy of sulfur is lower than that of phosphorus, despite sulfur having a greater nuclear charge. [2 marks]
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解題
(b) Acceleration: The ions are accelerated by an electric field to give them all the same kinetic energy.
Detection: The positive ions reach the detector (detector plate) and gain electrons to become neutral atoms. This movement of electrons generates an electrical current.
Abundance: The size of the current is proportional to the abundance of that isotope.
(c)(i) Z belongs to Group 15 (Group 5). This is because there is a very large increase (jump) between the 5th and 6th ionization energies, indicating that the 6th electron is removed from an inner quantum shell closer to the nucleus.
(ii) Equation: \(Z^{2+}(g) \to Z^{3+}(g) + e^-\)
(d)(i) Z is phosphorus (P). Full electronic configuration: \(1s^2 2s^2 2p^6 3s^2 3p^3\)
(ii) Phosphide ion (\(P^{3-}\)): \(1s^2 2s^2 2p^6 3s^2 3p^6\)
(e) Phosphorus has a \(3p^3\) configuration where each of the three 3p orbitals is singly occupied. Sulfur has a \(3p^4\) configuration with one pair of electrons in a 3p orbital. The repulsion between these paired electrons in sulfur (spin-pair repulsion) makes it easier to remove an electron than from phosphorus.
評分準則
- M1: Correct calculation setup: \(\frac{(69.0 \times 60.1) + (71.0 \times 39.9)}{100}\) (1)
- M2: Relative atomic mass = 69.80 (must be to 2 d.p.) (1)
- M3: Gallium / Ga (1)
(b)
- M1: Accelerated by an electric field / accelerated to have the same kinetic energy (1)
- M2: Detection: ions hit a detector plate / gain an electron (1)
- M3: Generating a current (1)
- M4: Size of current is proportional to the abundance of the isotope (1)
(c)(i)
- M1: Group 15 / Group 5 (1)
- M2: Because of the large jump between the 5th and 6th ionization energy (indicating 5 outer electrons) (1)
(c)(ii)
- M1: \(Z^{2+} \to Z^{3+} + e^-\) (1)
- M2: State symbols \((g)\) on both gaseous ions (1)
(d)
- M1: \(1s^2 2s^2 2p^6 3s^2 3p^3\) (do not accept [Ne]) (1)
- M2: \(1s^2 2s^2 2p^6 3s^2 3p^6\) (1)
(e)
- M1: Sulfur has a paired electron in a 3p orbital whereas phosphorus has singly occupied 3p orbitals (1)
- M2: Spin-pair repulsion in sulfur makes it easier to remove the electron (1)
(a) Define the term 'first electron affinity'. [2 marks]
(b) Use the following data to calculate the lattice energy of magnesium fluoride, \(\text{MgF}_2(s)\). [4 marks]
- Enthalpy change of formation of \(\text{MgF}_2(s)\) = \(-1124\text{ kJ mol}^{-1}\)
- Enthalpy change of atomisation of \(\text{Mg}(s)\) = \(+148\text{ kJ mol}^{-1}\)
- First ionisation energy of \(\text{Mg}(g)\) = \(+738\text{ kJ mol}^{-1}\)
- Second ionisation energy of \(\text{Mg}(g)\) = \(+1451\text{ kJ mol}^{-1}\)
- Bond enthalpy of \(\text{F}-\text{F}\) in \(\text{F}_2(g)\) = \(+158\text{ kJ mol}^{-1}\)
- First electron affinity of \(\text{F}(g)\) = \(-328\text{ kJ mol}^{-1}\)
(c) The experimental lattice energy of magnesium iodide, \(\text{MgI}_2\), is \(-2327\text{ kJ mol}^{-1}\), whereas the theoretical value calculated using an ionic model is \(-1944\text{ kJ mol}^{-1}\).
(i) Explain why there is a significant difference between the experimental and theoretical lattice energy values for magnesium iodide. [3 marks]
(ii) Explain why the difference between experimental and theoretical lattice energy values is much smaller for magnesium fluoride than for magnesium iodide. [2 marks]
(d) Use electron-pair repulsion theory to predict the shapes and bond angles of the following molecules:
(i) \(\text{BF}_3\). Explain your answer. [2 marks]
(ii) \(\text{NF}_3\). Explain your answer. [2 marks]
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解題
(b) Using a Born-Haber cycle:
\(\Delta H_f^\ominus = \Delta H_{at}^\ominus(\text{Mg}) + 1st\text{ IE}(\text{Mg}) + 2nd\text{ IE}(\text{Mg}) + \text{Bond Enthalpy of F}_2 + 2 \times 1st\text{ EA}(\text{F}) + \Delta H_{lattice}^\ominus\)
\(-1124 = +148 + 738 + 1451 + 158 + 2 \times (-328) + \Delta H_{lattice}^\ominus\)
\(-1124 = 2495 - 656 + \Delta H_{lattice}^\ominus\)
\(-1124 = 1839 + \Delta H_{lattice}^\ominus\)
\(\Delta H_{lattice}^\ominus = -1124 - 1839 = -2963\text{ kJ mol}^{-1}\).
(c)(i) Magnesium iodide has covalent character. The magnesium ion (\(\text{Mg}^{2+}\)) has a high charge density and strongly polarizes the large, highly polarizable iodide ion (\(\text{I}^-\)), causing distortion of its electron cloud and creating covalent character. The theoretical model assumes 100% ionic bonding.
(ii) The fluoride ion (\(\text{F}^-\)) is much smaller and has a much lower polarizability than the iodide ion. Therefore, there is negligible polarization and magnesium fluoride is almost purely ionic.
(d)(i) \(\text{BF}_3\): Shape: Trigonal planar. Bond angle: 120 degrees. Explanation: Boron has 3 bonding pairs and 0 lone pairs of electrons. These pairs repel each other equally to be as far apart as possible.
(ii) \(\text{NF}_3\): Shape: Trigonal pyramidal. Bond angle: 107 degrees (accept 102 - 108 degrees). Explanation: Nitrogen has 3 bonding pairs and 1 lone pair of electrons. Lone pair-bonding pair repulsion is greater than bonding pair-bonding pair repulsion, pushing the bonds closer together.
評分準則
- M1: Enthalpy change when 1 mole of gaseous atoms gains 1 mole of electrons (1)
- M2: To form 1 mole of gaseous 1- ions (1)
(b)
- M1: Correctly showing that 1 mole of fluorine molecules is atomized, using 158 kJ/mol (or 2 x 79 kJ/mol) (1)
- M2: Correctly multiplying electron affinity of fluorine by 2: \(2 \times -328 = -656\text{ kJ mol}^{-1}\) (1)
- M3: Rearranging the equation correctly: \(\Delta H_{lattice} = -1124 - (148 + 738 + 1451 + 158 - 656)\) (1)
- M4: Answer of \(-2963\text{ kJ mol}^{-1}\) (with unit and sign) (1)
(c)(i)
- M1: Magnesium iodide has significant covalent character / is not purely ionic (1)
- M2: \(\text{Mg}^{2+}\) has high charge density and polarizes the iodide ion (1)
- M3: Iodide ion is large and easily polarized / its electron cloud is distorted (1)
(c)(ii)
- M1: Fluoride ion is smaller and less polarizable than iodide (1)
- M2: Magnesium fluoride is almost 100% ionic / has negligible covalent character (1)
(d)(i)
- M1: Shape: Trigonal planar and angle: 120 degrees (1)
- M2: Explanation: 3 bonding pairs of electrons repel each other to maximum separation (1)
(d)(ii)
- M1: Shape: Trigonal pyramidal and angle: 107 degrees (accept 102-108 degrees) (1)
- M2: Explanation: 3 bonding pairs and 1 lone pair; lone pair repels bonding pairs more than bonding-bonding repulsion (1)
(a) But-2-ene reacts with hydrogen bromide (HBr) to form a single organic product.
(i) State the IUPAC name of the organic product. [1 mark]
(ii) Write the mechanism for this reaction, using curly arrows to show the movement of electron pairs. Include all partial charges (dipoles), lone pairs, and the structure of the intermediate carbocation. [4 marks]
(b) When propene reacts with HBr, two structural isomers are formed: a major product and a minor product.
(i) Identify both products and state which is the major product. [2 marks]
(ii) Explain, in terms of the stability of carbocation intermediates, why the major product is formed in greater abundance. [3 marks]
(c) But-2-ene exists as two stereoisomers.
(i) Draw the skeletal formulae of both stereoisomers of but-2-ene and clearly label each with its IUPAC stereochemical prefix (E or Z). [2 marks]
(ii) Explain why but-2-ene exhibits stereoisomerism, whereas but-1-ene does not. [3 marks]
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解題
(ii) Mechanism:
- The double bond (electron-rich \(\pi\) cloud) attacks the hydrogen of \(\text{H}^{\delta+}-\text{Br}^{\delta-}\). A curly arrow starts from the middle of the \(\text{C}=\text{C}\) bond to the \(\text{H}\) atom.
- The bond in \(\text{H-Br}\) breaks heterolytically. A curly arrow goes from the \(\text{H-Br}\) bond to the \(\text{Br}\) atom.
- A carbocation intermediate (\(\text{CH}_3\text{CH}_2\text{C}^+\text{HCH}_3\)) and a bromide ion (\(\text{Br}^-\)) with a lone pair are formed.
- A curly arrow goes from the lone pair on \(\text{Br}^-\) to the positively charged carbon of the carbocation to form the final product, 2-bromobutane.
(b)(i) Major product: 2-bromopropane. Minor product: 1-bromopropane.
(ii) The major product, 2-bromopropane, is formed via the more stable secondary carbocation intermediate (\(\text{CH}_3\text{C}^+\text{HCH}_3\)). The minor product, 1-bromopropane, is formed via the less stable primary carbocation intermediate (\(\text{CH}_3\text{CH}_2\text{C}^+\text{H}_2\)). Secondary carbocations are more stable because there are two electron-donating alkyl (methyl) groups that reduce the positive charge on the carbon atom (inductive effect), whereas primary carbocations have only one.
(c)(i) Draw skeletal formulae:
- E-but-2-ene: A zig-zag structure with the two methyl groups pointing in opposite directions across the double bond (trans-like).
- Z-but-2-ene: A 'U'-shaped structure with the two methyl groups pointing in the same direction across the double bond (cis-like).
(ii) Stereoisomerism (specifically geometric / E-Z isomerism) arises because there is restricted rotation around the \(\text{C}=\text{C}\) double bond due to the presence of the \(\pi\) bond. Additionally, each carbon of the double bond must be attached to two different groups. In but-2-ene, both double-bonded carbons are bonded to \(-\text{H}\) and \(-\text{CH}_3\) (two different groups). In but-1-ene, one of the carbon atoms in the double bond is bonded to two identical hydrogen atoms, so it cannot exhibit stereoisomerism.
評分準則
- M1: 2-bromobutane (1)
(a)(ii)
- M1: Curly arrow from \(\text{C}=\text{C}\) double bond to \(\text{H}\) of \(\text{H-Br}\) with correct dipole \(\text{H}^{\delta+}-\text{Br}^{\delta-}\) shown (1)
- M2: Curly arrow from the \(\text{H-Br}\) bond to the \(\text{Br}\) (1)
- M3: Correct drawing of secondary carbocation intermediate and bromide ion with lone pair (1)
- M4: Curly arrow from the lone pair on \(\text{Br}^-\) to the \(\text{C}^+\) of the carbocation (1)
(b)(i)
- M1: Correct names: 2-bromopropane and 1-bromopropane (1)
- M2: Clearly states that 2-bromopropane is the major product (1)
(b)(ii)
- M1: Major product goes via secondary carbocation and minor via primary carbocation (1)
- M2: Secondary carbocations are more stable than primary carbocations (1)
- M3: Due to the electron-donating inductive effect of two alkyl groups (versus one) (1)
(c)(i)
- M1: Correct skeletal formula of E-but-2-ene with label (1)
- M2: Correct skeletal formula of Z-but-2-ene with label (1)
(c)(ii)
- M1: Restricted rotation about the \(\text{C}=\text{C}\) double bond / \(\pi\) bond prevents rotation (1)
- M2: Each carbon of the double bond must be bonded to two different groups (1)
- M3: But-2-ene has \(-\text{H}\) and \(-\text{CH}_3\) on each carbon, whereas but-1-ene has two identical \(-\text{H}\) atoms on one of the carbons (1)
WCH12 甲部
- A.-602
- B.-301
- C.-60.2
- D.-15.0
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解題
評分準則
- A.The magnesium ion has a larger ionic radius and polarises the carbonate ion less effectively.
- B.The magnesium ion has a smaller ionic radius and polarises the carbonate ion more effectively.
- C.The magnesium ion has a smaller ionic radius and is polarised by the carbonate ion more effectively.
- D.The carbonate ion polarises the magnesium ion more effectively because of its smaller size.
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解題
評分準則
- A.1-chlorobutane
- B.2-chloro-2-methylpropane
- C.2-iodo-2-methylpropane
- D.1-iodobutane
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解題
評分準則
- A.HF has the strongest London forces, while HCl has the weakest hydrogen bonding.
- B.HF has the strongest covalent bond, while HCl has the weakest permanent dipole-dipole forces.
- C.HF has hydrogen bonding, while HCl has the weakest permanent dipole-dipole forces of all the hydrogen halides.
- D.HF has hydrogen bonding, while HCl has the weakest London forces among the other hydrogen halides.
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解題
評分準則
- A.The distribution curve is unchanged, and the activation energy decreases.
- B.The peak of the distribution curve shifts to the right, and the activation energy decreases.
- C.The distribution curve is unchanged, and the activation energy increases.
- D.The peak of the distribution curve shifts to the left, and the activation energy decreases.
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解題
評分準則
- A.\(\text{I}_2\), \(\text{SO}_2\), \(\text{H}_2\text{S}\)
- B.\(\text{SO}_2\), \(\text{S}\), \(\text{H}_2\text{S}\)
- C.\(\text{HI}\), \(\text{S}\), \(\text{SO}_2\)
- D.\(\text{NaHSO}_4\), \(\text{SO}_2\), \(\text{I}_2\)
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解題
評分準則
- A.Propan-1-ol
- B.Methyl ethanoate
- C.Propanoic acid
- D.3-hydroxypropanal
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解題
評分準則
- A.\(2\text{C(g)} + 6\text{H(g)} + \text{O(g)} \rightarrow \text{C}_2\text{H}_5\text{OH(l)}\)
- B.\(2\text{C(s, graphite)} + 3\text{H}_2\text{(g)} + \frac{1}{2}\text{O}_2\text{(g)} \rightarrow \text{C}_2\text{H}_5\text{OH(g)}\)
- C.\(\text{C}_2\text{H}_4\text{(g)} + \text{H}_2\text{O(l)} \rightarrow \text{C}_2\text{H}_5\text{OH(l)}\)
- D.\(2\text{C(s, graphite)} + 3\text{H}_2\text{(g)} + \frac{1}{2}\text{O}_2\text{(g)} \rightarrow \text{C}_2\text{H}_5\text{OH(l)}\)
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解題
評分準則
- A.1-chlorobutane reacts fastest because the C-Cl bond is the most polar, making the carbon most susceptible to nucleophilic attack.
- B.1-iodobutane reacts fastest because the C-I bond has the lowest bond enthalpy and is easiest to break.
- C.1-chlorobutane reacts slowest because chlorine has the highest electronegativity, which hinders the nucleophilic substitution.
- D.1-iodobutane reacts slowest because the C-I bond is the longest and has the greatest steric hindrance.
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解題
評分準則
- A.Thermal stability increases because the ionic radius of the cation increases, which decreases its polarizing power and distorts the carbonate ion less.
- B.Thermal stability decreases because the ionic radius of the cation increases, which increases its polarizing power and distorts the carbonate ion more.
- C.Thermal stability increases because the electronegativity of the Group 2 elements increases down the group.
- D.Thermal stability decreases because the sum of the first and second ionization energies of the metals decreases down the group.
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解題
評分準則
- A.-11.8 kJ mol^{-1}
- B.-376 kJ mol^{-1}
- C.-752 kJ mol^{-1}
- D.+376 kJ mol^{-1}
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解題
評分準則
- A.\(\text{CH}_3\text{CH}_2\text{CH}_2\text{CHO}\)
- B.\(\text{CH}_3\text{CH}_2\text{CH}_2\text{CH}_2\text{OH}\)
- C.\((\text{CH}_3)_3\text{COH}\)
- D.\(\text{CH}_3\text{CH}_2\text{OCH}_2\text{CH}_3\)
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解題
評分準則
- A.The peak of the Maxwell-Boltzmann curve shifts to the right and more molecules have energy greater than the activation energy.
- B.The peak of the Maxwell-Boltzmann curve shifts to the left and the value of the activation energy is lowered.
- C.The shape of the Maxwell-Boltzmann curve remains unchanged, but a larger fraction of molecules have energy greater than or equal to \(E_{\text{cat}}\).
- D.The area under the Maxwell-Boltzmann curve increases because the rate of reaction increases.
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解題
評分準則
- A.Increasing the temperature of the system.
- B.Decreasing the temperature of the system.
- C.Increasing the total pressure of the system by decreasing the volume.
- D.Adding a catalyst to the mixture.
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解題
評分準則
- A.Alcohol
- B.Aldehyde
- C.Ketone
- D.Carboxylic acid
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解題
評分準則
- A.-1 and +1
- B.-1 and +3
- C.-1 and +5
- D.+1 and +5
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解題
評分準則
- A.To act as a nucleophile to hydrolyse the halogenoalkane.
- B.To act as a solvent allowing the halogenoalkane and the aqueous silver nitrate to mix.
- C.To prevent the precipitation of silver oxide.
- D.To increase the activation energy of the hydrolysis reaction.
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解題
評分準則
- A.The magnesium ion has a smaller ionic radius and higher charge density than the barium ion, so it polarises the nitrate ion more strongly.
- B.The magnesium ion has a larger ionic radius than the barium ion, making the lattice energy of magnesium nitrate lower.
- C.The nitrogen-oxygen bonds in the nitrate ion of magnesium nitrate are inherently weaker than those in barium nitrate.
- D.Magnesium nitrate is more stable because the electronegativity of magnesium is higher than that of barium.
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解題
評分準則
- A.\(-106\text{ kJ mol}^{-1}\)
- B.\(+106\text{ kJ mol}^{-1}\)
- C.\(-1540\text{ kJ mol}^{-1}\)
- D.\(-2326\text{ kJ mol}^{-1}\)
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解題
評分準則
- A.The peak shifts to the left and becomes higher.
- B.The peak shifts to the right and becomes higher.
- C.The peak shifts to the left and becomes lower.
- D.The peak shifts to the right and becomes lower.
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解題
評分準則
WCH12 乙部 & C
An organic compound X has the molecular formula \(C_4H_9Br\). When X is heated under reflux with aqueous sodium hydroxide, an alcohol Y (\(C_4H_{10}O\)) is formed. Alcohol Y is oxidized by heating under reflux with an excess of acidified potassium dichromate(VI) to form a carboxylic acid Z (\(C_4H_8O_2\)). When X is reacted with aqueous silver nitrate in ethanol, a pale cream precipitate forms slowly.
(a) Identify the structures of X, Y, and Z. Explain your reasoning, including how the structures are deduced from the chemical tests and oxidation products. [5 marks]
(b) A student plans to compare the rate of hydrolysis of 1-chlorobutane, 1-bromobutane, and 1-iodobutane.
(i) Describe the procedure the student should use, including the reagents and the condition needed to ensure a fair comparison. [3 marks]
(ii) State the order of the rate of hydrolysis from fastest to slowest, and explain this trend in terms of bond enthalpies and bond polarities. [4 marks]
(c) Under different conditions, 2-bromo-2-methylpropane undergoes elimination rather than nucleophilic substitution when reacted with potassium hydroxide.
(i) State the reagent and solvent condition required to favor elimination. [1 mark]
(ii) Draw the skeletal structure of the organic product of this elimination reaction and state its IUPAC name. [2 marks]
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解題
(a) Identification & Reasoning:
1. The reaction with aqueous silver nitrate in ethanol produces a pale cream precipitate slowly, which indicates the presence of bromide ions (formation of \(AgBr(s)\)). Thus, compound X is a bromoalkane.
2. When Y is oxidized under reflux with excess acidified potassium dichromate(VI) to form a carboxylic acid Z, it means Y must be a primary alcohol. Secondary alcohols would oxidize to ketones, and tertiary alcohols do not oxidize.
3. Since Y is a primary alcohol, the starting bromoalkane X must be a primary bromoalkane.
4. There are two primary bromoalkane isomers with formula \(C_4H_9Br\): 1-bromobutane or 1-bromo-2-methylpropane.
- If X is 1-bromobutane: \(CH_3CH_2CH_2CH_2Br\). Then Y is butan-1-ol: \(CH_3CH_2CH_2CH_2OH\), and Z is butanoic acid: \(CH_3CH_2CH_2COOH\).
- If X is 1-bromo-2-methylpropane: \((CH_3)_2CHCH_2Br\). Then Y is 2-methylpropan-1-ol: \((CH_3)_2CHCH_2OH\), and Z is 2-methylpropanoic acid: \((CH_3)_2CHCOOH\).
(b) (i) Procedure:
1. Add equal volumes/amounts (e.g., \(1\text{ cm}^3\)) of 1-chlorobutane, 1-bromobutane, and 1-iodobutane to separate test tubes.
2. Add a mutual solvent such as ethanol (to dissolve the halogenoalkanes) and aqueous silver nitrate solution to each test tube.
3. Place all test tubes in a water bath held at a constant temperature (e.g., \(50^\circ\text{C}\)) and record the time taken for a precipitate to appear in each test tube.
(b) (ii) Order & Explanation:
- Order: 1-iodobutane (fastest) > 1-bromobutane > 1-chlorobutane (slowest).
- The rate of hydrolysis depends on the strength of the carbon-halogen bond (bond enthalpy).
- Going down Group 7 from Cl to I, the atomic size increases, which weakens the orbital overlap in the C-X bond, increasing bond length and decreasing the C-X bond enthalpy (C-I is the weakest bond, C-Cl is the strongest).
- Although the C-Cl bond is the most polar due to the higher electronegativity of chlorine (which would attract nucleophiles faster), bond enthalpy is the dominant factor. The C-I bond requires the least energy to break, so it reacts the fastest.
(c) (i) Elimination Conditions:
Concentrated potassium hydroxide (or sodium hydroxide) dissolved in ethanol (ethanolic) and heating under reflux.
(c) (ii) Product:
The skeletal structure of the product is a three-carbon chain with a double bond and a methyl group on the middle carbon. The IUPAC name is methylpropene (or 2-methylpropene).
評分準則
(a) [5 marks total]
- Deduce X is a bromoalkane due to cream precipitate of \(AgBr\) with silver nitrate. (1)
- Deduce Y is a primary alcohol because it oxidizes to a carboxylic acid. (1)
- Identify that X must be a primary bromoalkane. (1)
- State correct names/structures for X, Y, and Z for one isomer set: either 1-bromobutane, butan-1-ol, and butanoic acid OR 1-bromo-2-methylpropane, 2-methylpropan-1-ol, and 2-methylpropanoic acid. (2 marks for all three correct; 1 mark if only one or two are correct).
(b)(i) [3 marks total]
- Use equal volumes/amounts of each halogenoalkane and add ethanol and silver nitrate. (1)
- Control temperature using a water bath. (1)
- Measure the time taken for the precipitate to appear to determine rate. (1)
(b)(ii) [4 marks total]
- State correct order: 1-iodobutane > 1-bromobutane > 1-chlorobutane. (1)
- Identify that C-X bond enthalpy decreases down the group / C-I bond is the weakest. (1)
- Identify that C-Cl bond is the most polar. (1)
- State that bond enthalpy is the deciding factor / C-I bond is broken most easily. (1)
(c)(i) [1 mark total]
- Potassium hydroxide in ethanol / ethanolic KOH AND heating under reflux. (1)
(c)(ii) [2 marks total]
- Correct skeletal structure of methylpropene showing the double bond and branched methyl group. (1)
- Correct IUPAC name: methylpropene / 2-methylpropene. (1)
A student carried out an experiment to determine the enthalpy change of neutralisation, \(\Delta H_{neut}\), for the reaction between dilute hydrochloric acid, \(HCl(aq)\), and aqueous sodium hydroxide, \(NaOH(aq)\).
\(50.0\text{ cm}^3\) of \(1.00\text{ mol dm}^{-3}\) hydrochloric acid was mixed with \(50.0\text{ cm}^3\) of \(1.05\text{ mol dm}^{-3}\) sodium hydroxide solution in a polystyrene cup. The initial temperature of both solutions was \(18.5^\circ\text{C}\). The maximum temperature reached was \(25.2^\circ\text{C}\).
(a) (i) Calculate the heat energy released, \(q\), in joules. State any assumptions made about the density and specific heat capacity of the solutions. [3 marks]
(ii) Calculate the enthalpy change of neutralisation, \(\Delta H_{neut}\), in \(\text{kJ mol}^{-1}\) of water formed. Give your answer to 3 significant figures and include a sign. [4 marks]
(b) (i) Suggest two reasons, other than heat loss to the surroundings, why the experimental value obtained in part (a)(ii) might differ from the standard literature value of \(-57.1\text{ kJ mol}^{-1}\). [2 marks]
(ii) Explain why the enthalpy change of neutralisation of a weak acid, such as ethanoic acid, with sodium hydroxide is less exothermic than that of a strong acid. [2 marks]
(c) The standard enthalpy of formation of liquid ethanol, \(C_2H_5OH(l)\), can be determined using Hess's Law and standard enthalpies of combustion.
The standard enthalpies of combustion, \(\Delta H_c^\ominus\), are given in the table below:
Substance\(\Delta H_c^\ominus\) / \(\text{kJ mol}^{-1}\)\(C(s, graphite)\)\(-393.5\)\(H_2(g)\)\(-285.8\)\(C_2H_5OH(l)\)\(-1367.3\)(i) Write the chemical equation, including state symbols, for the reaction representing the standard enthalpy of formation of liquid ethanol. [2 marks]
(ii) Draw a Hess's Law cycle and calculate the standard enthalpy of formation of liquid ethanol, \(\Delta H_f^\ominus[C_2H_5OH(l)]\). [2 marks]
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解題
(a) (i) Heat energy calculation:
Total volume of solution = \(50.0 + 50.0 = 100.0\text{ cm}^3\).
Assume the density of the solution is the same as that of water, \(1.00\text{ g cm}^{-3}\), so mass \(m = 100.0\text{ g}\).
Assume the specific heat capacity of the solution is the same as water, \(c = 4.18\text{ J g}^{-1}\text{ K}^{-1}\).
Temperature rise, \(\Delta T = 25.2 - 18.5 = 6.7^\circ\text{C} = 6.7\text{ K}\).
\(q = m c \Delta T = 100.0 \times 4.18 \times 6.7 = 2800.6\text{ J}\) (or \(2.80\text{ kJ}\)).
(a) (ii) Enthalpy of neutralisation:
Moles of \(HCl\) used = \(\frac{50.0}{1000} \times 1.00 = 0.0500\text{ mol}\).
Moles of \(NaOH\) used = \(\frac{50.0}{1000} \times 1.05 = 0.0525\text{ mol}\).
Since \(HCl\) is the limiting reactant, moles of water formed = \(0.0500\text{ mol}\).
\(\Delta H_{neut} = - \frac{q}{\text{moles of water}} = - \frac{2800.6\text{ J}}{0.0500\text{ mol}} = -56012\text{ J mol}^{-1} = -56.0\text{ kJ mol}^{-1}\) (to 3 sig figs).
(b) (i) Reasons for difference:
1. Some heat was absorbed by the polystyrene cup and the thermometer (heat capacity of calorimeter not being negligible).
2. Inaccurate measurements of solution volumes or concentrations (experimental uncertainty).
3. The density and specific heat capacity of the actual aqueous mixtures are slightly different from those of pure water.
(b) (ii) Weak acid neutralisation:
Ethanoic acid is a weak acid and is only partially dissociated in aqueous solution.
Some energy is absorbed to fully dissociate the weak acid molecules into \(H^+\) and \(CH_3COO^-\) ions (as dissociation is an endothermic process). This reduces the net heat released to the surroundings, making the overall process less exothermic.
(c) (i) Formation Equation:
\(2C(s, graphite) + 3H_2(g) + \frac{1}{2}O_2(g) \rightarrow C_2H_5OH(l)\)
(c) (ii) Hess's Law calculation:
From Hess's Cycle using combustion values:
\(\Delta H_f^\ominus[C_2H_5OH(l)] = \sum \Delta H_c^\ominus(\text{Reactants}) - \sum \Delta H_c^\ominus(\text{Products})\)
\(\Delta H_f^\ominus = [2 \times (-393.5) + 3 \times (-285.8)] - [-1367.3]\)
\(\Delta H_f^\ominus = [-787.0 - 857.4] + 1367.3 = -1644.4 + 1367.3 = -277.1\text{ kJ mol}^{-1}\).
評分準則
(a)(i) [3 marks total]
- Calculates temperature change correctly: \(\Delta T = 6.7^\circ\text{C}\). (1)
- Calculates heat energy correctly: \(q = 2800.6\text{ J}\) (or \(2.80\text{ kJ}\)). (1)
- States both assumptions: density of solution is \(1.00\text{ g cm}^{-3}\) and specific heat capacity is \(4.18\text{ J g}^{-1}\text{ K}^{-1}\). (1)
(a)(ii) [4 marks total]
- Calculates moles of \(HCl = 0.0500\text{ mol}\) and moles of \(NaOH = 0.0525\text{ mol}\). (1)
- Identifies \(HCl\) is the limiting reactant, so moles of water formed = \(0.0500\text{ mol}\). (1)
- Calculates value of enthalpy change: \(\frac{2.8006}{0.0500} = 56.0\text{ kJ mol}^{-1}\). (1)
- Correctly applies negative sign and 3 significant figures: \(-56.0\text{ kJ mol}^{-1}\). (1)
(b)(i) [2 marks total]
- Accept any two reasonable points: heat absorbed by the calorimeter / thermometer (1); density/heat capacity of solutions is not exactly that of pure water (1); uncertainty in temperature reading (1).
(b)(ii) [2 marks total]
- Weak acids are only partially dissociated in solution. (1)
- Energy is required/absorbed to complete the dissociation of the acid molecules, making the overall process less exothermic. (1)
(c)(i) [2 marks total]
- Balanced chemical equation for formation: \(2C + 3H_2 + 0.5O_2 \rightarrow C_2H_5OH\). (1)
- All state symbols correct: \(C(s)\) (or graphite), \(H_2(g)\), \(O_2(g)\), \(C_2H_5OH(l)\). (1)
(c)(ii) [2 marks total]
- Shows correct Hess's cycle or algebraic formulation: \(2 \times \Delta H_c[C] + 3 \times \Delta H_c[H_2] - \Delta H_c[C_2H_5OH]\). (1)
- Correct answer with units: \(-277.1\text{ kJ mol}^{-1}\). (1)
This question is about Group 2 and Group 7 elements and their compounds.
(a) The thermal stability of the Group 2 nitrates increases down the group.
(i) Write a balanced chemical equation for the thermal decomposition of anhydrous magnesium nitrate. Include state symbols. [2 marks]
(ii) Explain, in terms of the charge and size of the cations, why magnesium nitrate decomposes at a lower temperature than barium nitrate. [4 marks]
(b) Chlorine is used in water treatment, where it undergoes a disproportionation reaction.
(i) Write the equation for the reaction of chlorine with cold water. Explain why this reaction is classified as disproportionation, referring to oxidation numbers. [4 marks]
(ii) State the hazard associated with using chlorine in drinking water treatment and explain why chlorine is used despite this hazard. [2 marks]
(c) Solid sodium halides react with concentrated sulfuric acid.
(i) When solid sodium iodide reacts with concentrated sulfuric acid, several products are formed including a gas with a smell of bad eggs and a purple vapour. Identify these two products and state the role of sulfuric acid in their formation. [3 marks]
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解題
(a) (i) Equation:
\(2Mg(NO_3)_2(s) \rightarrow 2MgO(s) + 4NO_2(g) + O_2(g)\)
(a) (ii) Explanation:
1. The magnesium ion (\(Mg^{2+}\)) has a smaller ionic radius than the barium ion (\(Ba^{2+}\)).
2. Both ions have the same charge (+2).
3. Therefore, the magnesium ion has a higher charge density than the barium ion.
4. This higher charge density polarizes and distorts the electron cloud of the nitrate ion (\(NO_3^-\)) more strongly, weakening the covalent oxygen-nitrogen bonds within the nitrate ion, which allows it to decompose at a lower temperature.
(b) (i) Disproportionation:
Equation: \(Cl_2(aq) + H_2O(l) \rightleftharpoons HCl(aq) + HClO(aq)\)
- The oxidation number of chlorine in elemental chlorine (\(Cl_2\)) is 0.
- In hydrochloric acid (\(HCl\)), the oxidation number of chlorine is -1.
- In chloric(I) acid (\(HClO\)), the oxidation number of chlorine is +1.
- Since chlorine has been simultaneously oxidized (from 0 to +1) and reduced (from 0 to -1) in the same chemical reaction, it is a disproportionation reaction.
(b) (ii) Hazard and Benefit:
- Hazard: Chlorine is highly toxic/poisonous and can react with organic compounds in water to form chlorinated organic compounds, which are carcinogenic.
- Benefit: The benefits of killing pathogenic microorganisms (such as bacteria causing cholera and typhoid) outweigh the extremely low risks associated with the concentrations of chlorine used.
(c) (i) Sodium Iodide and Sulfuric Acid:
- The gas with a smell of bad eggs is hydrogen sulfide, \(H_2S\).
- The purple vapour is iodine, \(I_2\).
- Sulfuric acid acts as an oxidizing agent (it oxidizes iodide ions, \(I^-\), to free iodine, while being reduced to hydrogen sulfide).
評分準則
(a)(i) [2 marks total]
- Correct formulae and balancing: \(2Mg(NO_3)_2 \rightarrow 2MgO + 4NO_2 + O_2\). (1)
- Correct state symbols: \((s)\) for reactants/solid products and \((g)\) for gases. (1)
(a)(ii) [4 marks total]
- State that \(Mg^{2+}\) has a smaller ionic radius / ionic size than \(Ba^{2+}\). (1)
- State both cations have the same (+2) charge. (1)
- Conclude \(Mg^{2+}\) has a higher charge density. (1)
- Explain that \(Mg^{2+}\) polarizes / distorts the nitrate ion electron cloud more, weakening the N-O bond. (1)
(b)(i) [4 marks total]
- Correct equation: \(Cl_2 + H_2O \rightleftharpoons HCl + HClO\). (1)
- State that chlorine in \(Cl_2\) is at oxidation state 0. (1)
- State that chlorine in \(HCl\) is at -1 AND in \(HClO\) is at +1. (1)
- Define disproportionation as the simultaneous oxidation and reduction of the same element in a single reaction. (1)
(b)(ii) [2 marks total]
- State hazard: chlorine is toxic / poisonous / forms toxic chlorinated hydrocarbons. (1)
- State benefit: kills bacteria / sterilises water, and the benefits outweigh the risks. (1)
(c)(i) [3 marks total]
- Identify hydrogen sulfide (\(H_2S\)). (1)
- Identify iodine (\(I_2\)). (1)
- Identify the role of sulfuric acid as an oxidizing agent. (1)
This question is about chemical kinetics and equilibria.
(a) The Maxwell-Boltzmann distribution curves represent the molecular energies in a gas at two different temperatures, \(T_1\) and \(T_2\).
(i) Describe how you would draw a sketch of the Maxwell-Boltzmann distribution of molecular energies for a fixed mass of gas at temperature \(T_1\), and explain how this distribution shifts at a higher temperature, \(T_2\). Your description should explain the key features of the axes, the shape of the curves, and how the activation energy, \(E_a\), is represented. [4 marks]
(ii) Explain why the rate of reaction increases significantly with a relatively small increase in temperature. [3 marks]
(b) Methanol can be synthesised industrially from carbon monoxide and hydrogen in a reversible reaction:
\(CO(g) + 2H_2(g) \rightleftharpoons CH_3OH(g) \quad \Delta H = -91\text{ kJ mol}^{-1}\)
(i) State and explain the effect of increasing the total pressure on the equilibrium yield of methanol. [2 marks]
(ii) State and explain the effect of increasing the temperature on the equilibrium yield of methanol. [2 marks]
(iii) In industry, this reaction is carried out at a compromise temperature of about \(250^\circ\text{C}\) and a pressure of about \(50\text{ to }100\text{ atm}\) in the presence of a copper-based catalyst. Explain why a compromise temperature and pressure are used rather than high pressure and low temperature, which would maximize the yield. [4 marks]
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解題
(a) (i) Maxwell-Boltzmann Distribution Features:
1. Axes: The y-axis represents the number of molecules (or fraction of molecules) with a given energy, and the x-axis represents the molecular kinetic energy.
2. Shape at \(T_1\): The curve starts at the origin \((0,0)\), rises to a peak (most probable energy), and then tails off gradually towards the right at higher energies, but never touches the x-axis.
3. Shift at higher temperature \(T_2\): The curve shifts to the right; the peak is lower and broader. The total area under both curves remains identical (representing the same number of molecules).
4. Activation Energy, \(E_a\): Marked as a vertical line on the high-energy tail of the x-axis. The area under the curve to the right of this line represents the number of molecules with energy equal to or greater than \(E_a\).
(a) (ii) Temperature and Rate:
1. At temperature \(T_2\), a much larger fraction of molecules have kinetic energy equal to or greater than the activation energy (\(E \ge E_a\)), which is shown by a larger area under the curve to the right of \(E_a\).
2. Therefore, upon collision, a significantly greater proportion of collisions are successful.
3. Additionally, the molecules move faster, leading to a higher frequency of collisions (though the increase in successful proportion of collisions is the dominant factor).
(b) (i) Effect of Pressure:
- Yield of methanol increases.
- According to Le Chatelier's principle, an increase in pressure shifts the equilibrium in the direction that decreases the pressure, which is towards the side with fewer gas molecules (there are 3 moles of gas on the left and only 1 mole on the right).
(b) (ii) Effect of Temperature:
- Yield of methanol decreases.
- The forward reaction is exothermic (\(\Delta H = -91\text{ kJ mol}^{-1}\)). An increase in temperature shifts the equilibrium to the left (the endothermic direction) to absorb the added thermal energy.
(b) (iii) Compromise Conditions in Industry:
1. Low Temperature: Although low temperature favors a high yield of methanol, the rate of reaction would be extremely slow, making the process economically unviable as it takes too long to reach equilibrium.
2. High Pressure: Although high pressure increases both the rate and the equilibrium yield, generating and maintaining very high pressures requires very expensive thick-walled reactors and compressors, and presents a high safety risk.
3. Compromise: A compromise temperature of \(250^\circ\text{C}\) and pressure of \(50-100\text{ atm}\) provide a sufficient reaction rate and reasonable yield while ensuring cost-effectiveness and safety.
4. Catalyst: The use of a copper catalyst speeds up the rate of reaction, allowing equilibrium to be reached much faster at this moderate compromise temperature.
評分準則
(a)(i) [4 marks total]
- Labels axes correctly (y-axis: number/fraction of molecules; x-axis: energy). (1)
- Describes curve starting at the origin, having an asymmetrical peak, and tailing off without touching the x-axis. (1)
- Describes high-temperature curve (\(T_2\)) as having a lower peak shifted to the right. (1)
- Explains that activation energy \(E_a\) is a vertical line and the area to its right represents molecules with \(E \ge E_a\). (1)
(a)(ii) [3 marks total]
- State that only molecules with energy \(E \ge E_a\) can react upon collision. (1)
- State that at higher temperature, a much larger proportion / fraction of molecules have energy \(E \ge E_a\). (1)
- Conclude that this results in a higher frequency of successful collisions. (1)
(b)(i) [2 marks total]
- State that equilibrium yield increases. (1)
- Explain that increasing pressure shifts the system to the side with fewer gas moles (3 moles reactant vs 1 mole product). (1)
(b)(ii) [2 marks total]
- State that equilibrium yield decreases. (1)
- Explain that the forward reaction is exothermic, so the equilibrium shifts to the left to absorb heat. (1)
(b)(iii) [4 marks total]
- Explains why low temp is not used: rate is too slow. (1)
- Explains why high pressure is not used: high costs of equipment/energy and safety hazards. (1)
- States that compromise conditions balance rate, yield, and safety/cost. (1)
- States the catalyst increases the rate, allowing a lower, safer, and cheaper compromise temperature to be used. (1)
部分 WCH13 Practical Papers
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WCH14 甲部
\[2A + B \rightarrow C + D\]
The rate equation is found to be:
\[\text{Rate} = k[A][B]^2\]
In an experiment, the initial concentrations of A and B are both \(0.10\text{ mol dm}^{-3}\) and the initial rate is \(r\).
If the experiment is repeated with the initial concentration of A doubled and the initial concentration of B halved, what is the new initial rate of reaction?
- A.\(\frac{r}{4}\)
- B.\(\frac{r}{2}\)
- C.\(r\)
- D.\(2r\)
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解題
When the concentration of A is doubled, \([A]_1 = 2 \times 0.10 = 0.20\text{ mol dm}^{-3}\).
When the concentration of B is halved, \([B]_1 = 0.5 \times 0.10 = 0.05\text{ mol dm}^{-3}\).
The new rate is:
\[r' = k[A]_1[B]_1^2 = k(0.20)(0.05)^2 = k(0.20)(0.0025) = k(0.00050)\]
Comparing \(r'\) with \(r\):
\[\frac{r'}{r} = \frac{0.00050}{0.0010} = 0.5\]
Therefore, the new initial rate of reaction is \(\frac{r}{2}\).
評分準則
\[\text{N}_2(\text{g}) + 3\text{H}_2(\text{g}) \rightleftharpoons 2\text{NH}_3(\text{g})\]
**Given data:**
* \(\Delta S_{\text{system}}^{\ominus} = -198.3\text{ J K}^{-1}\text{ mol}^{-1}\)
* \(\Delta H^{\ominus} = -92.2\text{ kJ mol}^{-1}\) (at \(298\text{ K}\))
- A.\(-507.7\text{ J K}^{-1}\text{ mol}^{-1}\)
- B.\(-111.1\text{ J K}^{-1}\text{ mol}^{-1}\)
- C.\(+111.1\text{ J K}^{-1}\text{ mol}^{-1}\)
- D.\(+507.7\text{ J K}^{-1}\text{ mol}^{-1}\)
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解題
\[\Delta S_{\text{surroundings}} = -\frac{\Delta H}{T}\]
Convert \(\Delta H\) from \(\text{kJ mol}^{-1}\) to \(\text{J mol}^{-1}\):
\[\Delta H = -92.2 \times 10^3\text{ J mol}^{-1} = -92200\text{ J mol}^{-1}\]
\[\Delta S_{\text{surroundings}} = -\frac{-92200}{298} = +309.4\text{ J K}^{-1}\text{ mol}^{-1}\]
Now, calculate \(\Delta S_{\text{total}}\):
\[\Delta S_{\text{total}} = \Delta S_{\text{system}} + \Delta S_{\text{surroundings}}\]
\[\Delta S_{\text{total}} = -198.3 + 309.4 = +111.1\text{ J K}^{-1}\text{ mol}^{-1}\]
評分準則
\[2\text{SO}_2(\text{g}) + \text{O}_2(\text{g}) \rightleftharpoons 2\text{SO}_3(\text{g}) \quad \Delta H = -197\text{ kJ mol}^{-1}\]
Which of the following changes will increase the value of the equilibrium constant, \(K_p\)?
- A.Increasing the total pressure of the system.
- B.Decreasing the temperature of the system.
- C.Adding a catalyst.
- D.Increasing the partial pressure of \(\text{O}_2(\text{g})\).
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解題
Because the forward reaction is exothermic (\(\Delta H < 0\)), lowering the temperature of the system shifts the equilibrium to the right to oppose the change, producing more products and increasing the value of \(K_p\).
評分準則
The acid dissociation constant, \(K_{\text{a}}\), for propanoic acid is \(1.30 \times 10^{-5}\text{ mol dm}^{-3}\) at \(298\text{ K}\).
What is the ratio of \(\frac{[\text{propanoate ions}]}{[\text{propanoic acid}]}\) in this buffer solution?
- A.0.12
- B.0.82
- C.1.22
- D.8.20
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解題
\[\text{pH} = \text{p}K_{\text{a}} + \log_{10}\left(\frac{[\text{A}^-]}{[\text{HA}]}\right)\]
First, calculate \(\text{p}K_{\text{a}}\):
\[\text{p}K_{\text{a}} = -\log_{10}(1.30 \times 10^{-5}) = 4.886\]
Substitute the given pH and the calculated \(\text{p}K_{\text{a}}\) into the equation:
\[4.80 = 4.886 + \log_{10}\left(\frac{[\text{A}^-]}{[\text{HA}]}\right)\]
\[\log_{10}\left(\frac{[\text{A}^-]}{[\text{HA}]}\right) = 4.80 - 4.886 = -0.086\]
\[\frac{[\text{A}^-]}{[\text{HA}]} = 10^{-0.086} = 0.820\]
評分準則
Which of the following statements about this reaction is correct?
- A.The reaction is a nucleophilic substitution.
- B.The product mixture rotates the plane of plane-polarised light.
- C.The reaction involves attack by a \(\text{CN}^-\)\ nucleophile on the planar carbonyl carbon atom from either side with equal probability.
- D.The reaction occurs more rapidly at a pH below 3.
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解題
B: The product mixture is a racemic mixture and is therefore optically inactive.
C: Correct. The planar carbonyl carbon of propanal can be attacked with equal probability from either side by the nucleophile (\(\text{CN}^-\)), yielding equal amounts of both enantiomers (a racemic mixture).
D: At very low pH, the cyanide ions are protonated to form HCN, lowering the concentration of the \(\text{CN}^-\) nucleophile and slowing down the reaction.
評分準則
- A.Propanal
- B.Propan-2-ol
- C.Pentan-2-one
- D.Pentan-3-one
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解題
2. The compound must be capable of being reduced to a secondary alcohol. Therefore, the starting compound must be a ketone.
3. Combining these two requirements, the compound must be a methyl ketone.
* Propanal (aldehyde) reduces to a primary alcohol.
* Propan-2-ol is already an alcohol and cannot be reduced to a secondary alcohol.
* Pentan-2-one (\(\text{CH}_3\text{COCH}_2\text{CH}_2\text{CH}_3\)) is a methyl ketone; it gives a positive iodoform test and reduces to the secondary alcohol pentan-2-ol.
* Pentan-3-one (\(\text{CH}_3\text{CH}_2\text{COCH}_2\text{CH}_3\)) is a ketone but not a methyl ketone, so it does not give a positive iodoform test.
評分準則
What is the activation energy, \(E_{\text{a}}\), for this reaction?
(Gas constant, \(R = 8.31\text{ J K}^{-1}\text{ mol}^{-1}\))
- A.\(+1.02 \times 10^{-3}\text{ kJ mol}^{-1}\)
- B.\(+1.02\text{ kJ mol}^{-1}\)
- C.\(+70.6\text{ kJ mol}^{-1}\)
- D.\(+70.6\text{ J mol}^{-1}\)
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解題
\[\ln k = -\frac{E_{\text{a}}}{R} \left(\frac{1}{T}\right) + \ln A\]
Thus, a plot of \(\ln k\) against \(\frac{1}{T}\) yields a straight line with:
\[\text{gradient} = -\frac{E_{\text{a}}}{R}\]
\[-8.50 \times 10^3 = -\frac{E_{\text{a}}}{8.31}\]
\[E_{\text{a}} = 8.50 \times 10^3 \times 8.31 = 70635\text{ J mol}^{-1}\]
Convert to \(\text{kJ mol}^{-1}\):
\[E_{\text{a}} = +70.6\text{ kJ mol}^{-1}\]
評分準則
- A.1.00
- B.1.70
- C.2.00
- D.7.00
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解題
\[n(\text{H}^+) = \frac{30.0 \times 0.100}{1000} = 0.00300\text{ mol}\]
\[n(\text{OH}^-) = \frac{20.0 \times 0.100}{1000} = 0.00200\text{ mol}\]
2. Determine the excess reactant after neutralisation:
\[\text{Excess } n(\text{H}^+) = 0.00300 - 0.00200 = 0.00100\text{ mol}\]
3. Calculate the total volume of the mixture:
\[V_{\text{total}} = 20.0 + 30.0 = 50.0\text{ cm}^3 = 0.0500\text{ dm}^3\]
4. Calculate the concentration of \(\text{H}^+\) ions:
\[[\text{H}^+] = \frac{0.00100\text{ mol}}{0.0500\text{ dm}^3} = 0.0200\text{ mol dm}^{-3}\]
5. Calculate the pH:
\[\text{pH} = -\log_{10}(0.0200) \approx 1.70\]
評分準則
- A.\(1.2 \text{ dm}^6 \text{ mol}^{-2} \text{ s}^{-1}\)
- B.\(1.2 \text{ dm}^3 \text{ mol}^{-1} \text{ s}^{-1}\)
- C.\(0.12 \text{ dm}^6 \text{ mol}^{-2} \text{ s}^{-1}\)
- D.\(0.12 \text{ dm}^3 \text{ mol}^{-1} \text{ s}^{-1}\)
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- A.\(+99.7 \text{ kJ mol}^{-1}\)
- B.\(-99.7 \text{ kJ mol}^{-1}\)
- C.\(+1.44 \text{ kJ mol}^{-1}\)
- D.\(+9.97 \times 10^4 \text{ kJ mol}^{-1}\)
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解題
評分準則
- A.\(-242.8 \text{ J K}^{-1} \text{ mol}^{-1}\)
- B.\(+242.8 \text{ J K}^{-1} \text{ mol}^{-1}\)
- C.\(-312.7 \text{ J K}^{-1} \text{ mol}^{-1}\)
- D.\(-37.8 \text{ J K}^{-1} \text{ mol}^{-1}\)
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解題
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- A.Above \(386 \text{ K}\)
- B.Below \(386 \text{ K}\)
- C.Above \(0.386 \text{ K}\)
- D.Below \(0.386 \text{ K}\)
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- A.\(0.296 \text{ atm}^{-2}\)
- B.\(3.38 \text{ atm}^2\)
- C.\(0.667 \text{ atm}^{-2}\)
- D.\(2.67 \text{ atm}^{-2}\)
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解題
評分準則
- A.\(4.44\)
- B.\(5.05\)
- C.\(4.74\)
- D.\(2.72\)
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評分準則
- A.\(1.60\)
- B.\(1.40\)
- C.\(3.00\)
- D.\(1.00\)
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- A.\(\text{CH}_3\text{COCH}_2\text{CH}_3\)
- B.\(\text{CH}_3\text{CH}_2\text{CH}_2\text{CHO}\)
- C.\((\text{CH}_3)_2\text{CHCHO}\)
- D.\(\text{CH}_2=\text{CHCH}_2\text{CH}_2\text{OH}\)
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解題
評分準則
- A.\(+99.7\)
- B.\(+1.44\)
- C.\(-99.7\)
- D.\(+9.97 \times 10^4\)
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解題
評分準則
- A.\(+16.0\text{ J K}^{-1}\text{ mol}^{-1}\)
- B.\(-175.8\text{ J K}^{-1}\text{ mol}^{-1}\)
- C.\(-368.0\text{ J K}^{-1}\text{ mol}^{-1}\)
- D.\(+368.0\text{ J K}^{-1}\text{ mol}^{-1}\)
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- A.4.57
- B.4.87
- C.5.17
- D.2.93
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- A.Pentan-3-one
- B.Pentan-2-one
- C.Pentanal
- D.Propanoic acid
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WCH14 乙部 & C
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評分準則
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WCH15 甲部
- A.Mn2+(aq)
- B.MnO4-(aq) in acidic conditions
- C.Cr2O72-(aq) in acidic conditions
- D.Cl2(g)
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解題
評分準則
- A.Cu+ is [Ar] 3d9 4s1 and Cr3+ is [Ar] 3d3
- B.Cu+ is [Ar] 3d10 and Cr3+ is [Ar] 3d3
- C.Cu+ is [Ar] 3d10 and Cr3+ is [Ar] 3d1 4s2
- D.Cu+ is [Ar] 3d9 4s1 and Cr3+ is [Ar] 3d1 4s2
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解題
評分準則
- A.Formula: [CuCl4]2-, Coordination number: 4, Geometry: Tetrahedral
- B.Formula: [CuCl6]4-, Coordination number: 6, Geometry: Octahedral
- C.Formula: [CuCl4]2-, Coordination number: 4, Geometry: Square planar
- D.Formula: [CuCl4(H2O)2]2-, Coordination number: 6, Geometry: Octahedral
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解題
評分準則
- A.Benzene
- B.Nitrobenzene
- C.Methylbenzene
- D.Benzoic acid
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解題
評分準則
- A.Ethylamine < Ammonia < Phenylamine
- B.Ammonia < Phenylamine < Ethylamine
- C.Phenylamine < Ammonia < Ethylamine
- D.Phenylamine < Ethylamine < Ammonia
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解題
評分準則
- A.\( \Delta S^\theta_{\text{total}} = \frac{nFE^\theta_{\text{cell}}}{T} \)
- B.\( \Delta S^\theta_{\text{total}} = -nFE^\theta_{\text{cell}}T \)
- C.\( \Delta S^\theta_{\text{total}} = \frac{-nFE^\theta_{\text{cell}}}{T} \)
- D.\( \Delta S^\theta_{\text{total}} = nFE^\theta_{\text{cell}}T \)
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解題
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- A.To remove insoluble impurities while preventing the organic product from crystallizing in the funnel
- B.To remove soluble impurities while preventing the organic product from crystallizing in the funnel
- C.To initiate rapid crystallization of the pure organic product
- D.To ensure that all soluble impurities are precipitated out of the solvent
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評分準則
- A.\( \text{CH}_3\text{CH}(\text{NH}_3^+)\text{COOH} \)
- B.\( \text{CH}_3\text{CH}(\text{NH}_3^+)\text{COO}^- \)
- C.\( \text{CH}_3\text{CH}(\text{NH}_2)\text{COO}^- \)
- D.\( \text{CH}_3\text{CH}(\text{NH}_2)\text{COOH} \)
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評分準則
- A.\(\text{Fe}^{2+}(aq)\) reducing \(\text{S}_4\text{O}_6^{2-}(aq)\)
- B.\(\text{I}^-(aq)\) reducing \(\text{Fe}^{3+}(aq)\)
- C.\(\text{S}_2\text{O}_3^{2-}(aq)\) reducing \(\text{I}^-(aq)\)
- D.\(\text{I}_2(aq)\) oxidizing \(\text{Fe}^{2+}(aq)\)
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解題
Reduction: \(\text{Fe}^{3+}(aq) + e^- \to \text{Fe}^{2+}(aq) \quad E^\ominus = +0.77 \text{ V}\)
Oxidation: \(2\text{I}^-(aq) \to \text{I}_2(aq) + 2e^- \quad E^\ominus = +0.54 \text{ V}\)
This gives \(E^\ominus_{\text{cell}} = +0.77 - 0.54 = +0.23 \text{ V}\). Since \(E^\ominus_{\text{cell}} > 0\), this reaction is thermodynamically feasible under standard conditions.
評分準則
- A.\(\text{V}^{3+}\)
- B.\(\text{Cr}^{3+}\)
- C.\(\text{Fe}^{2+}\)
- D.\(\text{Mn}^{2+}\)
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解題
\(\text{V}^{3+}\): \([\text{Ar}]3d^2\) (2 unpaired electrons)
\(\text{Cr}^{3+}\): \([\text{Ar}]3d^3\) (3 unpaired electrons)
\(\text{Fe}^{2+}\): \([\text{Ar}]3d^6\) (4 unpaired electrons, because one d-orbital is doubly occupied and four are singly occupied)
\(\text{Mn}^{2+}\): \([\text{Ar}]3d^5\) (5 unpaired electrons, because all five d-orbitals are singly occupied)
Therefore, \(\text{Mn}^{2+}\) has the highest number of unpaired d-electrons.
評分準則
- A.From +2 to +3
- B.From +3 to +4
- C.From +4 to +5
- D.From +2 to +4
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解題
- \(\text{V}^{2+}(aq)\) (oxidation state +2) is violet.
- \(\text{V}^{3+}(aq)\) (oxidation state +3) is green.
- \(\text{VO}^{2+}(aq)\) (oxidation state +4) is blue.
- \(\text{VO}_2^+(aq)\) (oxidation state +5) is yellow.
Thus, a color change from green to blue corresponds to oxidation from the +3 to the +4 oxidation state.
評分準則
- A.Propyloxybenzene
- B.1-phenylpropan-1-one
- C.1-phenylpropan-2-one
- D.Propylbenzene
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解題
評分準則
- A.Ammonia
- B.Phenylamine
- C.Ethylamine
- D.Diethylamine
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解題
評分準則
- A.\(\text{H}_2(g) + 2\text{OH}^-(aq) \to 2\text{H}_2\text{O}(l) + 2e^-\)
- B.\(\text{O}_2(g) + 2\text{H}_2\text{O}(l) + 4e^- \to 4\text{OH}^-(aq)\)
- C.\(\text{H}_2(g) \to 2\text{H}^+(aq) + 2e^-\)
- D.\(\text{O}_2(g) + 4\text{H}^+(aq) + 4e^- \to 2\text{H}_2\text{O}(l)\)
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解題
評分準則
- A.\(\text{C}_6\text{H}_5\text{N}=\text{NC}_6\text{H}_4\text{OH}\)
- B.\(\text{C}_6\text{H}_5\text{NHNHC}_6\text{H}_4\text{OH}\)
- C.\(\text{C}_6\text{H}_5\text{N}=\text{NC}_6\text{H}_5\)
- D.\(\text{C}_6\text{H}_5\text{NHCOC}_6\text{H}_4\text{OH}\)
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解題
評分準則
- A.The coordination number of copper(II) increases from 6 to 12.
- B.The enthalpy change of the reaction is highly positive.
- C.The system experiences a significant increase in entropy because the number of species in solution increases from 4 to 7.
- D.The copper-nitrogen bonds formed are much stronger than the copper-oxygen bonds broken.
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評分準則
- A.The coordination number changes from 6 to 4, and the geometry changes from octahedral to tetrahedral.
- B.The coordination number changes from 6 to 4, and the geometry changes from octahedral to square planar.
- C.The coordination number remains 6, and the geometry remains octahedral.
- D.The coordination number changes from 4 to 6, and the geometry changes from tetrahedral to octahedral.
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解題
評分準則
- A.Phenol and nitrogen
- B.Benzene and nitrogen
- C.Phenol and nitrogen dioxide
- D.Chlorobenzene and chlorine
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解題
評分準則
- A.\(Fe^{2+}\) reduces \(S_2O_8^{2-}\) to \(SO_4^{2-}\) and is oxidized to \(Fe^{3+}\); the resulting \(Fe^{3+}\) then oxidizes \(I^-\) to \(I_2\) and is reduced back to \(Fe^{2+}\). Both steps are thermodynamically feasible.
- B.\(Fe^{2+}\) oxidizes \(S_2O_8^{2-}\) to \(SO_4^{2-}\) and is reduced to \(Fe^+\); the resulting \(Fe^+\) then reduces \(I^-\) to \(I_2\) and is oxidized back to \(Fe^{2+}\). Both steps are thermodynamically feasible.
- C.\(Fe^{2+}\) reduces \(I^-\) to \(I_2\) and is oxidized to \(Fe^{3+}\); the resulting \(Fe^{3+}\) then oxidizes \(S_2O_8^{2-}\) to \(SO_4^{2-}\) and is reduced back to \(Fe^{2+}\). Both steps are thermodynamically feasible.
- D.\(Fe^{2+}\) adsorbs the reactant ions onto its surface, lowering the activation energy by weakening the bonds within the reactant ions.
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解題
評分準則
- A.Benzene, methylbenzene, phenol
- B.Phenol, methylbenzene, benzene
- C.Methylbenzene, benzene, phenol
- D.Benzene, phenol, methylbenzene
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評分準則
WCH15 乙部 & C
(a) Write the electronic configuration of vanadium in its +5 oxidation state and explain why V(V) compounds are usually colorless, whereas V(IV) compounds are blue.
(b) A student reduces a \(25.0\text{ cm}^3\) sample of \(0.0200\text{ mol dm}^{-3}\) ammonium vanadate(V) solution, \(\text{NH}_4\text{VO}_3\), using excess zinc under acidic conditions. After filtration to remove excess zinc, the solution is titrated with \(0.0100\text{ mol dm}^{-3}\) acidified potassium manganate(VII), \(\text{KMnO}_4\).
(i) Identify the oxidation state of vanadium after reduction with zinc.
(ii) State the color change at the end point of the titration.
(iii) Calculate the volume of \(\text{KMnO}_4\) solution required to oxidize the vanadium back to its +5 oxidation state.
(c) Explain why, when using tin instead of zinc, the vanadium is only reduced to the +3 oxidation state. Justify your answer using the standard electrode potentials below:
\(E^\theta(\text{Zn}^{2+}/\text{Zn}) = -0.76\text{ V}\)
\(E^\theta(\text{Sn}^{2+}/\text{Sn}) = -0.14\text{ V}\)
\(E^\theta(\text{V}^{3+}/\text{V}^{2+}) = -0.26\text{ V}\)
\(E^\theta(\text{VO}^{2+}/\text{V}^{3+}) = +0.34\text{ V}\)
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解題
(b)(i) +2
(b)(ii) Colorless to first permanent pale pink.
(b)(iii)
1. Moles of \(\text{VO}_3^-\): \(n(\text{V}) = 0.0250\text{ dm}^3 \times 0.0200\text{ mol dm}^{-3} = 5.00 \times 10^{-4}\text{ mol}\).
2. The oxidation state changes from +2 to +5. Therefore, each vanadium ion loses 3 electrons: \(\text{V}^{2+} \rightarrow \text{V}^{5+} + 3e^-\).
3. Total moles of electrons transferred: \(3 \times 5.00 \times 10^{-4}\text{ mol} = 1.50 \times 10^{-3}\text{ mol}\).
4. Manganate(VII) ions are reduced: \(\text{MnO}_4^- + 8\text{H}^+ + 5e^- \rightarrow \text{Mn}^{2+} + 4\text{H}_2\text{O}\).
5. Moles of \(\text{MnO}_4^-\) required: \(\frac{1.50 \times 10^{-3}\text{ mol}}{5} = 3.00 \times 10^{-4}\text{ mol}\).
6. Volume of \(\text{KMnO}_4\): \(V = \frac{3.00 \times 10^{-4}\text{ mol}}{0.0100\text{ mol dm}^{-3}} = 0.0300\text{ dm}^3 = 30.0\text{ cm}^3\).
(c) For reduction to occur, the overall cell potential \(E^\theta_{\text{cell}}\) must be positive (\(E^\theta_{\text{cell}} > 0\)).
- Zinc can reduce \(\text{V}^{3+}\) to \(\text{V}^{2+}\) because: \(E^\theta_{\text{cell}} = E^\theta(\text{V}^{3+}/\text{V}^{2+}) - E^\theta(\text{Zn}^{2+}/\text{Zn}) = -0.26 - (-0.76) = +0.50\text{ V}\). Since this value is positive, the reaction is thermodynamically feasible.
- Tin cannot reduce \(\text{V}^{3+}\) to \(\text{V}^{2+}\) because: \(E^\theta_{\text{cell}} = E^\theta(\text{V}^{3+}/\text{V}^{2+}) - E^\theta(\text{Sn}^{2+}/\text{Sn}) = -0.26 - (-0.14) = -0.12\text{ V}\). Since this value is negative, the reaction is not feasible.
- However, tin can reduce \(\text{VO}^{2+}\) to \(\text{V}^{3+}\) because: \(E^\theta_{\text{cell}} = E^\theta(\text{VO}^{2+}/\text{V}^{3+}) - E^\theta(\text{Sn}^{2+}/\text{Sn}) = +0.34 - (-0.14) = +0.48\text{ V}\). Since this value is positive, the reaction is feasible and the reduction stops at the +3 state.
評分準則
- 1 mark: Correct electronic configuration of vanadium(V) as \(1s^2 2s^2 2p^6 3s^2 3p^6\) or \([\text{Ar}]3d^0\).
- 1 mark: V(V) is colorless because there are no 3d electrons, so no d-d transitions are possible.
- 1 mark: V(IV) has a \(3d^1\) configuration and the d-orbitals are split into different energy levels by ligands.
- 1 mark: Electrons are excited/promoted by absorbing specific wavelengths of light, and the complementary blue color is seen.
(b)(i) [1 mark]
- 1 mark: +2 (allow V2+ / V(II))
(b)(ii) [1 mark]
- 1 mark: Colorless to (first permanent pale/light) pink (reject purple)
(b)(iii) [5.5 marks]
- 1 mark: Calculate moles of V(V) = \(5.00 \times 10^{-4}\text{ mol}\)
- 1.5 marks: Deduces moles of electrons lost = \(3 \times 5.00 \times 10^{-4} = 1.50 \times 10^{-3}\text{ mol}\) (1 mark for multiplying by 3, 0.5 mark for correct calculation)
- 1 mark: Moles of \(\text{MnO}_4^-\)= \(1.50 \times 10^{-3} / 5 = 3.00 \times 10^{-4}\text{ mol}\)
- 1 mark: Correct calculation of volume of \(\text{KMnO}_4\) = \(30.0\text{ cm}^3\)
- 1 mark: Correct use of units and 3 significant figures.
(c) [6 marks]
- 1 mark: States that a reaction is feasible if \(E^\theta_{\text{cell}}\) is positive (or \(E^\theta\) of the reduction half-reaction is more positive than that of the oxidation half-reaction).
- 2 marks: Calculates \(E^\theta_{\text{cell}} = +0.50\text{ V}\) for zinc reducing \(\text{V}^{3+}\) to \(\text{V}^{2+}\) and concludes this is feasible.
- 2 marks: Calculates \(E^\theta_{\text{cell}} = -0.12\text{ V}\) for tin reducing \(\text{V}^{3+}\) to \(\text{V}^{2+}\) and concludes this is not feasible.
- 1 mark: Calculates \(E^\theta_{\text{cell}} = +0.48\text{ V}\) for tin reducing \(\text{VO}^{2+}\) to \(\text{V}^{3+}\) to show it stops at +3.
(a) Phenylalanine exists as a zwitterion in the solid state.
(i) Draw the structure of the zwitterion of phenylalanine.
(ii) Draw the structures of the organic products formed when phenylalanine reacts with:
- Excess \(\text{CH}_3\text{COCl}\)
- Excess \(\text{CH}_3\text{OH}\) in the presence of concentrated \(\text{H}_2\text{SO}_4\) catalyst
- Excess aqueous sodium hydroxide, \(\text{NaOH}\)
(b) Explain the difference in basicity between phenylamine, ethylamine, and ammonia. Arrange them in order of increasing basic strength and justify your answer by referring to their electronic structures.
(c) Phenylalanine can be synthesized from phenylacetaldehyde (\(\text{C}_6\text{H}_5\text{CH}_2\text{CHO}\)) in a two-step pathway:
- Step 1: Phenylacetaldehyde is reacted with a mixture of \(\text{KCN}\) and \(\text{NH}_4\text{Cl}\) to form the aminonitrile, \(\text{C}_6\text{H}_5\text{CH}_2\text{CH(NH}_2)\text{CN}\).
- Step 2: The aminonitrile is hydrolyzed to form phenylalanine.
(i) Name the type of reaction mechanism in Step 1 and identify the formula of the carbon-containing nucleophile.
(ii) Give the reagents and conditions required for the hydrolysis in Step 2, and write the equation for this step under acidic conditions, showing the structures of the organic and inorganic nitrogen-containing products.
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解題
(a)(ii)
- With excess \(\text{CH}_3\text{COCl}\): \(\text{C}_6\text{H}_5\text{CH}_2\text{CH(NHCOCH}_3)\text{COOH}\)
- With excess \(\text{CH}_3\text{OH}/\text{H}^+\): \(\text{C}_6\text{H}_5\text{CH}_2\text{CH(NH}_3^+)\text{COOCH}_3\text{ Cl}^-\)
- With excess aqueous \(\text{NaOH}\): \(\text{C}_6\text{H}_5\text{CH}_2\text{CH(NH}_2)\text{COO}^- \text{Na}^+\)
(b) Order of increasing basicity: phenylamine < ammonia < ethylamine.
Basicity is a measure of the ability of the nitrogen lone pair to accept a proton (\(\text{H}^+\)).
- In phenylamine, the lone pair of electrons on the nitrogen atom is delocalized into the \(\pi\)-system of the benzene ring. This decreases the electron density on the nitrogen, making the lone pair less available to form a dative covalent bond with a proton.
- In ethylamine, the ethyl group is an electron-donating alkyl group (+I inductive effect). This increases the electron density on the nitrogen atom, making the lone pair more available to accept a proton compared to ammonia, which has no alkyl groups.
(c)(i) Mechanism: Nucleophilic addition. Nucleophile: \(\text{CN}^-\).
(c)(ii) Reagents and conditions: Heat under reflux with dilute hydrochloric acid (\(\text{HCl}\)) or dilute sulfuric acid (\(\text{H}_2\text{SO}_4\)).
Equation: \(\text{C}_6\text{H}_5\text{CH}_2\text{CH(NH}_2)\text{CN} + 2\text{H}_2\text{O} + 2\text{H}^+ \rightarrow \text{C}_6\text{H}_5\text{CH}_2\text{CH(NH}_3^+)\text{COOH} + \text{NH}_4^+\)
評分準則
- 1 mark: Correct zwitterion structure showing \(\text{NH}_3^+\) and \(\text{COO}^-\).
(a)(ii) [4.5 marks]
- 1.5 marks: Correct structure of \(\text{C}_6\text{H}_5\text{CH}_2\text{CH(NHCOCH}_3)\text{COOH}\) (amide group formed, carboxylic acid untouched).
- 1.5 marks: Correct structure of \(\text{C}_6\text{H}_5\text{CH}_2\text{CH(NH}_3^+)\text{COOCH}_3\) (ester formed and amine protonated, accept neutral amine if acid catalyst not specified as excess, but protonated is preferred).
- 1.5 marks: Correct structure of \(\text{C}_6\text{H}_5\text{CH}_2\text{CH(NH}_2)\text{COO}^-\text{ Na}^+\) (carboxylate salt formed, amine untouched).
(b) [6.5 marks]
- 1.5 marks: Correct order of basicity (phenylamine < ammonia < ethylamine).
- 1 mark: States basicity is due to the availability of the nitrogen lone pair to accept a proton.
- 2 marks: Explains phenylamine basicity (delocalization of nitrogen lone pair into benzene \(\pi\)-system decreases its availability).
- 2 marks: Explains ethylamine basicity (electron-releasing/donating ethyl group (+I effect) increases electron density on nitrogen, making the lone pair more available).
(c)(i) [1.5 marks]
- 1 mark: Nucleophilic addition (reject nucleophilic substitution).
- 0.5 mark: \(\text{CN}^-\).
(c)(ii) [4 marks]
- 1 mark: Dilute hydrochloric acid (or dilute sulfuric acid).
- 1 mark: Heat under reflux.
- 2 marks: Correct balanced equation: \(\text{C}_6\text{H}_5\text{CH}_2\text{CH(NH}_2)\text{CN} + 2\text{H}_2\text{O} + 2\text{H}^+ \rightarrow \text{C}_6\text{H}_5\text{CH}_2\text{CH(NH}_3^+)\text{COOH} + \text{NH}_4^+\) (1 mark for organic product showing protonated amine, 1 mark for balanced equation/inorganic ammonium ion).
(a) When hydrated copper(II) sulfate is dissolved in water, a pale blue solution containing \([\text{Cu(H}_2\text{O)}_6]^{2+}\) is formed.
(i) Define the term *ligand* and explain how a coordinate bond is formed between a ligand and a transition metal ion.
(ii) Describe and explain why transition metal complexes are colored, referring to d-orbital splitting, light absorption, and complementary colors.
(b) When concentrated hydrochloric acid is added to the pale blue solution of \([\text{Cu(H}_2\text{O)}_6]^{2+}\), a yellow-green solution of \([\text{CuCl}_4]^{2-}\) is formed.
(i) Write the equation for this ligand substitution reaction.
(ii) State and explain the change in coordination number and shape of the complex that occurs during this reaction.
(iii) Suggest why the coordination number changes.
(c) When excess aqueous ammonia is added to the original \([\text{Cu(H}_2\text{O)}_6]^{2+}\) solution, a deep blue solution is formed.
(i) Write the formula of the copper complex ion responsible for the deep blue color.
(ii) Explain why this reaction reaches an equilibrium and how the stability constant, \(K_{\text{stab}}\), of this complex compares to that of \([\text{Cu(H}_2\text{O)}_6]^{2+}\).
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解題
(a)(ii) In isolated transition metal ions, the 3d orbitals are degenerate (have the same energy). When ligands approach the transition metal ion, the d-orbitals are split into two groups of different energy levels (\(\Delta E\)). When visible light is shone on the complex, electrons in the lower energy d-orbitals absorb light of a specific frequency/wavelength and are promoted to a higher energy d-orbital (d-d transition). The energy absorbed is given by \(\Delta E = h\nu\). The remaining frequencies of light are transmitted (or reflected), and the complementary color of the absorbed light is observed.
(b)(i) \([\text{Cu(H}_2\text{O)}_6]^{2+} + 4\text{Cl}^- \rightleftharpoons [\text{CuCl}_4]^{2-} + 6\text{H}_2\text{O}\)
(b)(ii) The coordination number decreases from 6 to 4. The shape of the complex changes from octahedral (bond angles of \(90^\circ\)) to tetrahedral (bond angles of \(109.5^\circ\)).
(b)(iii) Chloride ligands (\(\text{Cl}^-\)) are larger than water molecules (\(\text{H}_2\text{O}\)) and have negative charges, leading to greater electrostatic and steric repulsion around the central copper(II) ion, which limits the number of ligands that can coordinate to 4.
(c)(i) \([\text{Cu(NH}_3)_4(\text{H}_2\text{O})_2]^{2+}\)
(c)(ii) The reaction is a reversible ligand substitution where ammonia ligands displace water ligands. The stability constant, \(K_{\text{stab}}\), is the equilibrium constant for the formation of the complex. The \([\text{Cu(NH}_3)_4(\text{H}_2\text{O})_2]^{2+}\) complex has a much larger stability constant compared to the hexaaquacopper(II) complex because ammonia is a stronger ligand/nucleophile than water, making the equilibrium position lie heavily to the right.
評分準則
- 1 mark: Define ligand as a species with a lone pair of electrons.
- 1.5 marks: Explain coordinate bond formation as the donation of a lone pair from the ligand to the vacant d-orbitals of the transition metal.
(a)(ii) [5 marks]
- 1 mark: Ligands split the 3d orbitals into two different energy levels.
- 1 mark: Electrons absorb light energy to transition from lower to higher energy levels (d-d transition).
- 1 mark: Use of \(\Delta E = h\nu\) or \(\Delta E = hc/\lambda\).
- 1 mark: The color observed is the complementary color of the absorbed light.
- 1 mark: Note that transition metals must have partially filled d-orbitals for this transition to be possible.
(b)(i) [1.5 marks]
- 1.5 marks: Fully balanced equation with correct charges: \([\text{Cu(H}_2\text{O)}_6]^{2+} + 4\text{Cl}^- \rightleftharpoons [\text{CuCl}_4]^{2-} + 6\text{H}_2\text{O}\) (allow 1 mark for unbalanced or missing state symbols, but charges must be correct).
(b)(ii) [3 marks]
- 1 mark: Coordination number changes from 6 to 4.
- 1 mark: Shape changes from octahedral to tetrahedral.
- 1 mark: Bond angles change from \(90^\circ\) to \(109.5^\circ\) (allow \(109^\circ\) to \(110^\circ\)).
(b)(iii) [1.5 marks]
- 1 mark: Chloride ions are larger than water molecules.
- 0.5 mark: Steric hindrance/repulsion between negatively charged chloride ligands restricts the coordination number.
(c)(i) [1 mark]
- 1 mark: \([\text{Cu(NH}_3)_4(\text{H}_2\text{O})_2]^{2+}\) (accept \([\text{Cu(NH}_3)_4]^{2+}\) if water ligands are omitted, but preferred is the dihydrate).
(c)(ii) [3 marks]
- 1 mark: Ligand substitution is a reversible/equilibrium process.
- 1 mark: \(K_{\text{stab}}\) represents the equilibrium constant for ligand exchange.
- 1 mark: The stability constant for the tetraamminediaphor-copper(II) complex is much higher than that of the hexaaqua complex because ammonia forms stronger coordinate bonds.
(a) In Step 1, benzene is nitrated to produce nitrobenzene.
(i) State the reagents and temperature required for this reaction.
(ii) Write the equation for the reaction of the reagents to generate the electrophile, \(\text{NO}_2^+\).
(iii) Draw the mechanism for the electrophilic substitution of benzene to form nitrobenzene, showing the movement of electrons with curly arrows and the structure of the intermediate.
(b) In Step 2, nitrobenzene is reduced to phenylamine. State the reagents and conditions needed for this reduction, and write a simplified chemical equation using \([\text{H}]\) to represent the reducing agent.
(c) In Step 3, phenylamine is converted into benzenediazonium chloride. State the reagents and temperature required, and explain why the temperature must be carefully controlled.
(d) In Step 4, benzenediazonium chloride is coupled with an alkaline solution of phenol to form 4-(phenyldiazenyl)phenol.
(i) Draw the structure of 4-(phenyldiazenyl)phenol.
(ii) Explain why azo dyes are highly colored, referring to their molecular structure.
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解題
Temperature: \(50^\circ\text{C}\) to \(55^\circ\text{C}\).
(a)(ii) \(\text{HNO}_3 + 2\text{H}_2\text{SO}_4 \rightarrow \text{NO}_2^+ + 2\text{HSO}_4^- + \text{H}_3\text{O}^+\) (or \(\text{HNO}_3 + \text{H}_2\text{SO}_4 \rightarrow \text{NO}_2^+ + \text{HSO}_4^- + \text{H}_2\text{O}\)).
(a)(iii)
- A curly arrow starts from the delocalized \(\pi\)-ring of benzene to the nitrogen atom of the \(\text{NO}_2^+\) electrophile.
- This forms a stable, positively charged intermediate (benzenonium ion) with a horseshoe-shaped partial delocalization ring that is open towards the \(\text{sp}^3\) carbon bearing the hydrogen and nitro group, and a \(+\) charge in the middle of the horseshoe.
- A curly arrow from the \(\text{C}-\text{H}\) bond of this carbon pointing back into the center of the ring restores the aromaticity.
- The products are nitrobenzene and a hydrogen ion (\(\text{H}^+\)).
(b) Reagents: Tin (\(\text{Sn}\)) and concentrated hydrochloric acid (\(\text{HCl}\)), followed by treatment with aqueous sodium hydroxide (\(\text{NaOH}\)) to liberate phenylamine.
Equation: \(\text{C}_6\text{H}_5\text{NO}_2 + 6[\text{H}] \rightarrow \text{C}_6\text{H}_5\text{NH}_2 + 2\text{H}_2\text{O}\).
(c) Reagents: Sodium nitrite (\(\text{NaNO}_2\)) and dilute hydrochloric acid (\(\text{HCl}\)) (to form nitrous acid, \(\text{HNO}_2\) in situ).
Temperature: Between \(0^\circ\text{C}\) and \(10^\circ\text{C}\).
Explanation: If the temperature is below \(0^\circ\text{C}\), the rate of reaction is too slow. If the temperature is above \(10^\circ\text{C}\), the benzenediazonium ion is highly unstable and decomposes rapidly to produce phenol and nitrogen gas (\(\text{N}_2\)).
(d)(i) The structure of 4-(phenyldiazenyl)phenol is:
\(\text{C}_6\text{H}_5-\text{N}=\text{N}-\text{C}_6\text{H}_4\text{OH}\) where the hydroxyl (\(\text{-OH}\)) group is in the para position (position 4) relative to the azo (\(\text{-N}=\text{N}-\)) group.
(d)(ii) Azo dyes are highly colored because they possess an extensive, highly conjugated \(\pi\)-electron system that spans across both benzene rings and the azo group. This delocalization narrows the energy gap between the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO). Consequently, the molecule can absorb light in the visible spectrum, and the complementary color of the absorbed wavelength is observed.
評分準則
- 1 mark: Concentrated \(\text{HNO}_3\) and concentrated \(\text{H}_2\text{SO}_4\).
- 1 mark: Temperature between \(50^\circ\text{C}\) and \(60^\circ\text{C}\) (reject if above \(60^\circ\text{C}\)).
(a)(ii) [1 mark]
- 1 mark: Correct equation for the generation of the electrophile.
(a)(iii) [4 marks]
- 1 mark: Curly arrow from the benzene ring to \(\text{NO}_2^+\).
- 2 marks: Correct structure of intermediate with horseshoe pointing to the substituted carbon, and positive charge inside the horseshoe.
- 1 mark: Curly arrow from \(\text{C}-\text{H}\) bond to ring, reforming the delocalized ring.
(b) [3 marks]
- 1 mark: Tin (\(\text{Sn}\)) and concentrated hydrochloric acid (\(\text{HCl}\)).
- 1 mark: Addition of sodium hydroxide (\(\text{NaOH}\)) to liberate the free amine.
- 1 mark: Balanced equation: \(\text{C}_6\text{H}_5\text{NO}_2 + 6[\text{H}] \rightarrow \text{C}_6\text{H}_5\text{NH}_2 + 2\text{H}_2\text{O}\).
(c) [3.5 marks]
- 1 mark: Sodium nitrite (\(\text{NaNO}_2\)) and hydrochloric acid (\(\text{HCl}\)) / nitrous acid (\(\text{HNO}_2\)).
- 0.5 mark: Temperature between \(0^\circ\text{C}\) and \(10^\circ\text{C}\).
- 1 mark: Explains that below \(0^\circ\text{C}\) the reaction is too slow.
- 1 mark: Explains that above \(10^\circ\text{C}\) the benzenediazonium ion decomposes to phenol and nitrogen.
(d)(i) [2 marks]
- 2 marks: Correct structure of 4-(phenyldiazenyl)phenol showing the \(\text{-N}=\text{N}-\) linker and the para-positioned \(\text{-OH}\) group on the second ring (1 mark for diazo linker, 1 mark for para-OH position).
(d)(ii) [2 marks]
- 1 mark: Explains that there is an extensive/extended conjugated \(\pi\)-system (involving both rings and the azo group).
- 1 mark: Explains that this delocalization reduces the HOMO-LUMO energy gap, allowing absorption of visible light.
部分 WCH16 Practical Papers
**Procedure:**
1. Dissolve 2.0 cm3 of methyl benzoate in 4.0 cm3 of concentrated sulfuric acid in a flask. Cool the mixture in an ice-water bath.
2. Prepare a nitrating mixture by carefully adding 1.5 cm3 of concentrated nitric acid to 1.5 cm3 of concentrated sulfuric acid. Cool this mixture in an ice-water bath.
3. Slowly add the nitrating mixture to the methyl benzoate solution, ensuring the temperature remains below 15 °C.
4. After the addition is complete, allow the mixture to stand at room temperature for 15 minutes, then pour it over 20 g of crushed ice.
5. Filter the resulting crude solid, wash it thoroughly with cold water, and recrystallise the solid using ethanol as the solvent.
6. Record the mass of the dry recrystallised methyl 3-nitrobenzoate (\(M_{\text{r}} = 181.15\)).
(a) Explain why it is important to keep the temperature below 15 °C during the addition of the nitrating mixture. (1)
(b) Describe the appearance of the mixture when it is poured onto the crushed ice in step 4. (1)
(c) State the role of the concentrated sulfuric acid in this reaction and write an equation for the formation of the electrophile. (2)
(d) Describe the steps involved in the recrystallisation of the crude methyl 3-nitrobenzoate from ethanol to obtain a pure, dry sample. (5)
(e) A student starts with 2.0 cm3 of methyl benzoate (density = 1.09 g cm\(^{-3}\), \(M_{\text{r}} = 136.15\)) and obtains 1.85 g of pure methyl 3-nitrobenzoate. Calculate the percentage yield of the product. (3)
(f) State how the student could confirm the purity of the obtained crystals using a simple physical technique. (1)
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解題
(b) A cream or white precipitate/solid is formed.
(c) Sulfuric acid acts as a catalyst / proton donor / acid catalyst.
Equation for electrophile generation:
\(\text{HNO}_3 + 2\text{H}_2\text{SO}_4 \rightarrow \text{NO}_2^+ + \text{H}_3\text{O}^+ + 2\text{HSO}_4^-\) (or \(\text{HNO}_3 + \text{H}_2\text{SO}_4 \rightarrow \text{NO}_2^+ + \text{H}_2\text{O} + \text{HSO}_4^-\)).
(d) Recrystallisation steps:
1. Dissolve the crude solid in the minimum volume of hot/boiling ethanol.
2. Filter the hot solution through fluted filter paper to remove insoluble impurities.
3. Allow the filtrate to cool slowly to room temperature, then place it in an ice bath to crystallise.
4. Filter the crystals under reduced pressure using a Buchner funnel and flask.
5. Wash the crystals with a small volume of cold ethanol and dry them in a desiccator or warm oven.
(e) Mass of methyl benzoate used = \(2.0 \times 1.09 = 2.18\text{ g}\).
Moles of methyl benzoate = \(2.18 / 136.15 = 0.01601\text{ mol}\).
Since the reaction stoichiometry is 1:1, theoretical moles of methyl 3-nitrobenzoate = \(0.01601\text{ mol}\).
Theoretical mass of methyl 3-nitrobenzoate = \(0.01601 \times 181.15 = 2.90\text{ g}\).
Percentage yield = \(\frac{1.85}{2.90} \times 100 = 63.8\%\) (or 64%).
(f) Measure the melting point of the crystals. Pure methyl 3-nitrobenzoate has a sharp melting point (at 78 °C) that matches the literature value.
評分準則
- To prevent further nitration / dinitration / formation of methyl 3,5-dinitrobenzoate.
(b) [1 mark]
- White / cream solid or precipitate.
(c) [2 marks]
- Role: Catalyst / proton donor [1].
- Equation: \(\text{HNO}_3 + 2\text{H}_2\text{SO}_4 \rightarrow \text{NO}_2^+ + \text{H}_3\text{O}^+ + 2\text{HSO}_4^-\) OR \(\text{HNO}_3 + \text{H}_2\text{SO}_4 \rightarrow \text{NO}_2^+ + \text{H}_2\text{O} + \text{HSO}_4^-\) [1].
(d) [5 marks]
- Dissolve in the minimum volume [1]
- of hot / boiling ethanol [1]
- Filter hot (to remove insoluble impurities) [1]
- Cool in ice (to crystallise) and filter under reduced pressure / using Buchner funnel [1]
- Wash with cold ethanol and dry [1].
(e) [3 marks]
- Mass of methyl benzoate = 2.18 g AND moles = 0.0160(1) mol [1]
- Theoretical mass = 2.90 g [1]
- Percentage yield = 63.8% (accept 63.8% to 64.0%) [1].
(f) [1 mark]
- Measure melting point which should be sharp and match literature values / 78 °C.
To determine the values of \(x\) and \(y\), two separate analytical procedures are carried out:
**Analysis 1: Gravimetric determination of sulfate ions**
A 0.950 g sample of the complex is dissolved in distilled water and acidified with dilute nitric acid. An excess of barium chloride solution, \(\text{BaCl}_2\text{(aq)}\), is added. The resulting precipitate of barium sulfate, \(\text{BaSO}_4\), is filtered, washed, dried, and weighed. The mass of the dry precipitate is 0.902 g.
**Analysis 2: Back-titration of ammonia**
Another 0.950 g sample of the complex is heated with excess aqueous sodium hydroxide. The liberated ammonia gas is distilled and absorbed completely into 50.00 cm3 of 0.500 mol dm\(^{-3}\) hydrochloric acid, \(\text{HCl}\).
The excess hydrochloric acid requires 38.15 cm3 of 0.250 mol dm\(^{-3}\) sodium hydroxide, \(\text{NaOH}\), for complete neutralisation.
(a) State why the solution is acidified with dilute nitric acid before adding barium chloride in Analysis 1. (1)
(b) Write the ionic equation, including state symbols, for the formation of the precipitate of barium sulfate. (1)
(c) Show by calculation that the number of moles of sulfate ions in the 0.950 g sample is \(3.86 \times 10^{-3}\) mol. (2)
(d) Calculate the number of moles of ammonia (\(\text{NH}_3\)) in the 0.950 g sample. (4)
(e) Determine the mass of water of crystallisation in the 0.950 g sample, and hence calculate the values of \(x\) and \(y\) in the formula.
(Relative atomic masses: \(\text{Cu} = 63.55\); \(\text{S} = 32.06\); \(\text{O} = 16.00\); \(\text{N} = 14.01\); \(\text{H} = 1.01\); \(\text{Ba} = 137.33\)) (4)
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解題
(b) \(\text{Ba}^{2+}\text{(aq)} + \text{SO}_4^{2-}\text{(aq)} \rightarrow \text{BaSO}_4\text{(s)}\)
(c) Molar mass of \(\text{BaSO}_4 = 137.33 + 32.06 + 4(16.00) = 233.39\text{ g mol}^{-1}\) (or 233.4).
Moles of \(\text{BaSO}_4 = \frac{0.902}{233.39} = 3.8648 \times 10^{-3}\text{ mol}\).
Since 1 mole of \(\text{SO}_4^{2-}\) produces 1 mole of \(\text{BaSO}_4\), the moles of \(\text{SO}_4^{2-}\) in the sample is indeed \(3.86 \times 10^{-3}\text{ mol}\) (to 3 s.f.).
(d) Initial moles of \(\text{HCl} = 0.05000 \times 0.500 = 0.02500\text{ mol}\).
Moles of \(\text{NaOH}\) used in the titration = \(0.03815 \times 0.250 = 9.5375 \times 10^{-3}\text{ mol}\).
Moles of excess \(\text{HCl}\) = moles of \(\text{NaOH}\) = \(9.5375 \times 10^{-3}\text{ mol}\).
Moles of \(\text{HCl}\) reacted with ammonia = \(0.02500 - 9.5375 \times 10^{-3} = 0.01546\text{ mol}\).
Since \(\text{NH}_3 + \text{HCl} \rightarrow \text{NH}_4\text{Cl}\), the moles of \(\text{NH}_3\) in the sample = \(0.01546\text{ mol}\) (or \(1.55 \times 10^{-2}\text{ mol}\)).
(e) Moles of \(\text{Cu}^{2+}\) must equal the moles of \(\text{SO}_4^{2-}\) to maintain neutrality: \(3.8648 \times 10^{-3}\text{ mol}\).
Let us find the mass of each component in the 0.950 g sample:
- Mass of \(\text{Cu}^{2+} = 3.8648 \times 10^{-3} \times 63.55 = 0.2456\text{ g}\)
- Mass of \(\text{SO}_4^{2-} = 3.8648 \times 10^{-3} \times 96.06 = 0.3712\text{ g}\)
- Mass of \(\text{NH}_3 = 0.01546 \times 17.04 = 0.2634\text{ g}\)
Total dry complex mass (excluding water) = \(0.2456 + 0.3712 + 0.2634 = 0.8802\text{ g}\).
Mass of water of crystallisation = \(0.950 - 0.8802 = 0.0698\text{ g}\).
Moles of \(\text{H}_2\text{O} = \frac{0.0698}{18.02} = 3.87 \times 10^{-3}\text{ mol}\).
Now find the mole ratios relative to \(\text{SO}_4^{2-}\):
- Ratio of \(\text{SO}_4^{2-} = \frac{3.8648 \times 10^{-3}}{3.8648 \times 10^{-3}} = 1\)
- Ratio of \(\text{NH}_3 = x = \frac{0.01546}{3.8648 \times 10^{-3}} = 4.00\)
- Ratio of \(\text{H}_2\text{O} = y = \frac{3.87 \times 10^{-3}}{3.8648 \times 10^{-3}} = 1.00\).
Therefore, \(x = 4\) and \(y = 1\).
評分準則
- To prevent precipitation of other ions like carbonate / sulfite (which form insoluble barium salts).
(b) [1 mark]
- \(\text{Ba}^{2+}\text{(aq)} + \text{SO}_4^{2-}\text{(aq)} \rightarrow \text{BaSO}_4\text{(s)}\) (including correct state symbols).
(c) [2 marks]
- Calculates molar mass of \(\text{BaSO}_4 = 233.39 / 233.4\text{ g mol}^{-1}\) [1]
- Moles of sulfate = \(0.902 / 233.39 = 3.86 \times 10^{-3}\text{ mol}\) [1].
(d) [4 marks]
- Calculates initial moles of HCl = 0.02500 mol [1]
- Calculates moles of NaOH / excess HCl = \(9.5375 \times 10^{-3}\text{ mol}\) [1]
- Calculates moles of reacted HCl = \(0.01546\text{ mol}\) [1]
- Moles of ammonia = \(0.01546\text{ mol}\) (accept 0.01546 to 0.0155) [1].
(e) [4 marks]
- Calculates mass of Cu, \(\text{SO}_4^{2-}\), and \(\text{NH}_3\) (or total mass = 0.880 g) [1]
- Calculates mass of \(\text{H}_2\text{O}\) = 0.070 g [1]
- Calculates moles of \(\text{H}_2\text{O}\) = \(3.87 \times 10^{-3}\text{ mol}\) [1]
- Finds ratio to get \(x = 4\) and \(y = 1\) [1].
\(\text{CH}_3\text{COCH}_3\text{(aq)} + \text{I}_2\text{(aq)} \xrightarrow{\text{H}^+\text{(aq)}} \text{CH}_3\text{COCH}_2\text{I(aq)} + \text{H}^+\text{(aq)} + \text{I}^-\text{(aq)}\)
(a) The student uses a colorimetric method. To do this, they must first construct a calibration curve.
Describe how the student would prepare five iodine solutions of different known concentrations from a standard 0.0100 mol dm\(^{-3}\) iodine solution using 100 cm3 volumetric flasks, and how these would be used to obtain the calibration curve. (4)
(b) Explain why a colorimeter is suitable for monitoring this reaction, and state the colour of the filter that should be used. (2)
(c) In one run, the student mixes 25.0 cm3 of 1.00 mol dm\(^{-3}\) propanone, 25.0 cm3 of 1.00 mol dm\(^{-3}\) sulfuric acid, and 50.0 cm3 of 0.0050 mol dm\(^{-3}\) iodine solution, and immediately starts a stop clock.
The student plots a graph of absorbance against time and obtains a straight line that decreases to zero.
(i) Deduce the order of reaction with respect to iodine, justifying your answer. (2)
(ii) Explain why the concentrations of propanone and sulfuric acid are chosen to be much larger than that of iodine. (1)
(d) In a second run, the student changes the concentration of propanone to find its order. The results of the two experiments are summarised below:
- **Experiment 1:** \([\text{propanone}] = 0.250\text{ mol dm}^{-3}\); Rate = \(1.20 \times 10^{-5}\text{ mol dm}^{-3}\text{ s}^{-1}\)
- **Experiment 2:** \([\text{propanone}] = 0.500\text{ mol dm}^{-3}\); Rate = \(2.40 \times 10^{-5}\text{ mol dm}^{-3}\text{ s}^{-1}\)
Given that the reaction is first-order with respect to \(\text{H}^+\), and that the concentration of \(\text{H}^+\) in both experiments is 0.500 mol dm\(^{-3}\):
- Deduce the order of reaction with respect to propanone.
- Calculate the value of the rate constant, \(k\), for the reaction.
- Include the units of \(k\). (4)
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解題
(b) Iodine is brown/yellow in aqueous solution, while the products are colourless, so the absorbance decreases as the reaction proceeds. A blue filter should be used (as blue is the complementary colour of yellow/brown, resulting in maximum absorbance).
(c) (i) The order with respect to iodine is zero. The straight-line graph of absorbance against time indicates a constant rate (i.e., the rate is independent of the iodine concentration).
(ii) To ensure that the concentrations of propanone and acid remain essentially constant during the reaction, so that any change in rate is solely due to the change in iodine concentration (flooding technique).
(d)
- Deduce order with respect to propanone:
When \([\text{propanone}]\) is doubled (from 0.250 to 0.500 mol dm\(^{-3}\)), the rate also doubles (from \(1.20 \times 10^{-5}\) to \(2.40 \times 10^{-5}\)). Thus, the reaction is first-order with respect to propanone.
- Rate equation:
\(\text{Rate} = k [\text{propanone}] [\text{H}^+]\)
- Calculate \(k\):
\(1.20 \times 10^{-5} = k \times 0.250 \times 0.500\)
\(1.20 \times 10^{-5} = 0.125 k\)
\(k = 9.60 \times 10^{-5}\)
- Units: \(\text{dm}^3\text{ mol}^{-1}\text{ s}^{-1}\).
評分準則
- Transfer known volumes of standard iodine using a pipette / burette [1]
- into five 100 cm3 volumetric flasks and make up to the mark with distilled/deionised water [1]
- Measure absorbance of each solution in the colorimeter [1]
- Plot absorbance against concentration to draw calibration curve [1].
(b) [2 marks]
- Iodine is coloured/brown and reactants/products are colourless / colorimeter monitors intensity of brown colour [1]
- Blue filter (accept blue-green) [1].
(c) [3 marks]
- (i) Zero order [1]
- because the graph of absorbance (concentration) against time is a straight line / has a constant gradient [1]
- (ii) To keep their concentrations virtually constant / so that they do not affect the rate during the run [1].
(d) [4 marks]
- Order with respect to propanone = 1st order, because doubling concentration doubles the rate [1]
- Rate equation: \(\text{Rate} = k [\text{propanone}] [\text{H}^+]\) [1]
- Calculation: \(k = 9.60 \times 10^{-5}\) [1]
- Units: \(\text{dm}^3\text{ mol}^{-1}\text{ s}^{-1}\) [1].
A student performs a series of chemical tests and spectroscopic analyses to determine the structure of **X**.
(a) Chemical Tests:
(i) Liquid **X** is added to a solution of 2,4-dinitrophenylhydrazine (2,4-DNPH). A bright orange precipitate is formed. State what information this test provides about the functional group present in **X**. (1)
(ii) Liquid **X** is warmed with Fehling's solution. The blue solution remains blue and no precipitate is observed. State what conclusion can be drawn from this result. (1)
(iii) State the name of another reagent that would give a similar negative result to Fehling's solution for compound **X**. (1)
(iv) State the IUPAC name of compound **X**. (1)
(b) If compound **X** was instead an isomer of formula \(\text{C}_4\text{H}_8\text{O}\) that reacted positively with Tollens' reagent, list the names of all possible structural isomers for this compound. (2)
(c) Spectroscopic analysis:
(i) Identify the wavenumber range and the bond responsible for the most intense peak in the infrared (IR) spectrum of **X**. (2)
(ii) Explain why there is no broad peak in the region \(3200 - 3750\text{ cm}^{-1}\) in the IR spectrum of **X**. (1)
(d) Mass Spectrometry:
In the mass spectrum of **X**, there is a major peak at \(m/z = 43\).
(i) Write the formula of the fragment ion responsible for this peak. (1)
(ii) Write an equation for the fragmentation of the molecular ion of **X** to form this species. (1)
(iii) State how you would use the mass spectrum to find the molar mass of **X**. (1)
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解題
(i) The presence of a carbonyl group / \(\text{C=O}\) / aldehyde or ketone.
(ii) **X** is not an aldehyde (it is a ketone).
(iii) Tollens' reagent (or acidified potassium dichromate(VI) / Benedict's solution).
(iv) Butanone (or butan-2-one).
(b) The isomers that are aldehydes are:
- Butanal
- Methylpropanal (or 2-methylpropanal).
(c)
(i) Range: \(1675 - 1750\text{ cm}^{-1}\) (or \(1665 - 1740\text{ cm}^{-1}\)). Bond: \(\text{C=O}\).
(ii) No \(\text{O-H}\) bond is present in the compound.
(d)
(i) \(\text{CH}_3\text{CO}^+\) (or \(\text{C}_3\text{H}_7^+\)).
(ii) \([\text{CH}_3\text{COCH}_2\text{CH}_3]^{+\bullet} \rightarrow \text{CH}_3\text{CO}^+ + \cdot\text{CH}_2\text{CH}_3\) (or \([\text{C}_4\text{H}_8\text{O}]^{+\bullet} \rightarrow \text{CH}_3\text{CO}^+ + \text{C}_2\text{H}_5^{\bullet}\)).
(iii) Find the \(m/z\) value of the molecular ion peak (\(\text{M}^+\)), which represents the molar mass.
評分準則
- (i) Carbonyl group / \(\text{C=O}\) present [1]
- (ii) Not an aldehyde / is a ketone [1]
- (iii) Tollens' reagent / Benedict's / acidified potassium dichromate(VI) [1]
- (iv) Butanone / butan-2-one [1].
(b) [2 marks]
- Butanal [1]
- Methylpropanal / 2-methylpropanal [1].
(c) [3 marks]
- (i) \(1665 - 1750\text{ cm}^{-1}\) [1]
- Carbonyl / \(\text{C=O}\) bond [1]
- (ii) No alcohol / carboxylic acid / no \(\text{O-H}\) bond present [1].
(d) [3 marks]
- (i) \(\text{CH}_3\text{CO}^+\) (or \(\text{C}_3\text{H}_7^+\)) [1] (charge must be shown)
- (ii) \([\text{CH}_3\text{COCH}_2\text{CH}_3]^{+\bullet} \rightarrow \text{CH}_3\text{CO}^+ + \cdot\text{CH}_2\text{CH}_3\) [1]
- (iii) Identify the molecular ion peak / \(\text{M}^+\) peak (highest m/z value excluding isotopic peaks) [1].
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