Hydrocarbons: WJEC A‑Level Chemistry questions
Every WJEC A-Level Chemistry exam question on 2.5 Hydrocarbons, 2016–2025, with its mark scheme and examiner’s report.
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Calculations
Q6(a)(i)
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Q6(a)(ii)
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Q8(a)(i)
The whole paper ↗![Summer 2025 Unit 4, question 8(a)(i): State the name of the reaction mechanism for this reaction. [1]](https://pub-e8a9dbab8e2a4d089f52b2a45e0d0b50.r2.dev/bank/1410u40-jun25-08-ai-qp.webp)
Q8(a)(ii)
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![Summer 2025 AS Unit 2, question 5: Name the compound shown by the structure drawn below. [2] CH3 H3C CH CH2CH3 C C H CH3](https://pub-e8a9dbab8e2a4d089f52b2a45e0d0b50.r2.dev/bank/2410u20-jun25-05-qp.webp)
Q7(a)(i)
The whole paper ↗![Summer 2025 AS Unit 2, question 7(a)(i): Name the mechanism for this reaction. [1]](https://pub-e8a9dbab8e2a4d089f52b2a45e0d0b50.r2.dev/bank/2410u20-jun25-07-ai-qp.webp)
Q7(a)(ii)
The whole paper ↗![Summer 2025 AS Unit 2, question 7(a)(ii): Give the reaction mechanism for the production of chloromethane from methane and chlorine. Show the initiation and propagation stages. [3] Initiation Propagatio](https://pub-e8a9dbab8e2a4d089f52b2a45e0d0b50.r2.dev/bank/2410u20-jun25-07-aii-qp.webp)
Q7(b)(i)
The whole paper ↗![Summer 2025 AS Unit 2, question 7(b)(i): Explain why the mixture produced in this reaction could contain ethane. [1]](https://pub-e8a9dbab8e2a4d089f52b2a45e0d0b50.r2.dev/bank/2410u20-jun25-07-bi-qp.webp)
Q7(b)(ii)
The whole paper ↗![Summer 2025 AS Unit 2, question 7(b)(ii): Explain why the mixture produced in this reaction could contain dichloromethane. [2]](https://pub-e8a9dbab8e2a4d089f52b2a45e0d0b50.r2.dev/bank/2410u20-jun25-07-bii-qp.webp)
Q7(c)(i)
The whole paper ↗![Summer 2025 AS Unit 2, question 7(c)(i): Suggest why this improvement could lead to fewer side-products in the mixture. [1]](https://pub-e8a9dbab8e2a4d089f52b2a45e0d0b50.r2.dev/bank/2410u20-jun25-07-ci-qp.webp)
Q7(c)(ii)
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Q10(a)(iii)
The whole paper ↗![Summer 2025 AS Unit 2, question 10(a)(iii): The but-1-ene formed during this reaction is then used to form 2-bromobutane by reaction with hydrogen bromide, HBr. Draw the mechanism for this reaction. [3]](https://pub-e8a9dbab8e2a4d089f52b2a45e0d0b50.r2.dev/bank/2410u20-jun25-10-aiii-qp.webp)
Q10(b)(ii)
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![Summer 2024 Unit 4, question 4: Give the formula of the triphenylmethyl radical. [1]](https://pub-e8a9dbab8e2a4d089f52b2a45e0d0b50.r2.dev/bank/1410u40-jun24-04-qp.webp)
Q7(b)(v)
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Q7(d)(iii)
The whole paper ↗![Summer 2024 Unit 4, question 7(d)(iii): Give the structure of the compound formed when compound J reacts with hydrogen bromide. [1]](https://pub-e8a9dbab8e2a4d089f52b2a45e0d0b50.r2.dev/bank/1410u40-jun24-07-diii-qp.webp)
Q4(a)
The whole paper ↗![Summer 2024 AS Unit 2, question 4(a): State why the chloroethene monomer does not exhibit E–Z isomerism. [1]](https://pub-e8a9dbab8e2a4d089f52b2a45e0d0b50.r2.dev/bank/2410u20-jun24-04-a-qp.webp)
Q4(b)
The whole paper ↗![Summer 2024 AS Unit 2, question 4(b): Draw the repeating unit for PVC. [1]](https://pub-e8a9dbab8e2a4d089f52b2a45e0d0b50.r2.dev/bank/2410u20-jun24-04-b-qp.webp)
![Summer 2024 AS Unit 2, question 5: Complete the equation to show the structure of the main product formed. [1] CH3CH CH2 + HBr](https://pub-e8a9dbab8e2a4d089f52b2a45e0d0b50.r2.dev/bank/2410u20-jun24-05-qp.webp)
![Summer 2024 AS Unit 2, question 7: Name the catalyst used in the hydrogenation of unsaturated oils to make saturated fats such as margarine. [1]](https://pub-e8a9dbab8e2a4d089f52b2a45e0d0b50.r2.dev/bank/2410u20-jun24-07-qp.webp)
All 73 questions on Hydrocarbons, as a list
- Summer 2025, Unit 4, Q6(a)(i) (1 mark): In ultraviolet light methane reacts with chlorine by a radical substitution reaction producing chloromethane and hydrogen chloride. CH4 + Cl2 CH3Cl + HCl Give t
- Summer 2025, Unit 4, Q6(a)(ii) (1 mark): Further chlorination of methane produces CH2Cl2, CHCl3 and CCl4. Give an equation to show how 1,2-dichloroethane might be another product of this chlorination r
- Summer 2025, Unit 4, Q8(a)(i) (1 mark): State the name of the reaction mechanism for this reaction. [1]
- Summer 2025, Unit 4, Q8(a)(ii) (1 mark): She predicted that the main product would be 2-bromopropanoic acid, rather than 3-bromopropanoic acid. Explain, in terms of carbocations, why 2-bromopropanoic a
- Summer 2025, AS Unit 2, Q5 (2 marks): Name the compound shown by the structure drawn below. [2] CH3 H3C CH CH2CH3 C C H CH3
- Summer 2025, AS Unit 2, Q7(a)(i) (1 mark): Name the mechanism for this reaction. [1]
- Summer 2025, AS Unit 2, Q7(a)(ii) (3 marks): Give the reaction mechanism for the production of chloromethane from methane and chlorine. Show the initiation and propagation stages. [3] Initiation Propagatio
- Summer 2025, AS Unit 2, Q7(b)(i) (1 mark): Explain why the mixture produced in this reaction could contain ethane. [1]
- Summer 2025, AS Unit 2, Q7(b)(ii) (2 marks): Explain why the mixture produced in this reaction could contain dichloromethane. [2]
- Summer 2025, AS Unit 2, Q7(c)(i) (1 mark): Suggest why this improvement could lead to fewer side-products in the mixture. [1]
- Summer 2025, AS Unit 2, Q7(c)(ii) (2 marks): This method was tested using different flow rates of the methane and chlorine mixture to find the best yield of chloromethane. The composition of the product mi
- Summer 2025, AS Unit 2, Q10(a)(iii) (3 marks): The but-1-ene formed during this reaction is then used to form 2-bromobutane by reaction with hydrogen bromide, HBr. Draw the mechanism for this reaction. [3]
- Summer 2025, AS Unit 2, Q10(b)(ii) (3 marks): Suggest which of the three possible products, A, B or C, would have the greatest yield. Explain your reasoning in terms of the stability of any carbocation inte
- Summer 2024, Unit 4, Q4 (1 mark): Give the formula of the triphenylmethyl radical. [1]
- Summer 2024, Unit 4, Q7(b)(v) (2 marks): The reaction product in stage 4, cyclohexadiene-1,4-dione acts as an alkene. I. State the type of reaction mechanism that occurs when an alkene reacts with brom
- Summer 2024, Unit 4, Q7(d)(iii) (1 mark): Give the structure of the compound formed when compound J reacts with hydrogen bromide. [1]
- Summer 2024, AS Unit 2, Q4(a) (1 mark): State why the chloroethene monomer does not exhibit E–Z isomerism. [1]
- Summer 2024, AS Unit 2, Q4(b) (1 mark): Draw the repeating unit for PVC. [1]
- Summer 2024, AS Unit 2, Q5 (1 mark): Complete the equation to show the structure of the main product formed. [1] CH3CH CH2 + HBr
- Summer 2024, AS Unit 2, Q7 (1 mark): Name the catalyst used in the hydrogenation of unsaturated oils to make saturated fats such as margarine. [1]
- Summer 2024, AS Unit 2, Q9(a) (2 marks): Calculate the empirical formula of A. [2] Empirical formula
- Summer 2024, AS Unit 2, Q13(a)(i) (2 marks): State the type of reaction involved in each case. [2] ethane and chlorine ethene and hydrogen chloride
- Summer 2024, AS Unit 2, Q13(a)(ii) (1 mark): Suggest why the reaction between ethene and hydrogen chloride gives the better yield. [1]
- Summer 2024, AS Unit 2, Q13(a)(iii) (4 marks): Give the mechanism for the reaction between ethene and hydrogen chloride. [4]
- Summer 2023, Unit 4, Q8(d) (1 mark): Tartaric acid is formed when butenedioic acid reacts with a suitable oxidising agent. Give the equation for this reaction, representing the oxidising agent as [
- Summer 2023, Unit 4, Q12(a)(i) (1 mark): State the type of mechanism occurring during the bromination. [1]
- Summer 2023, Unit 4, Q12(a)(iii) (1 mark): The dibromoacid produced in part (ii) is then reacted with zinc under suitable conditions to give 2-methylpropenoic acid. Complete the equation, showing zinc br
- Summer 2023, AS Unit 2, Q2 (1 mark): When fuels are burned with insufficient oxygen, incomplete combustion occurs and carbon monoxide is formed instead of carbon dioxide. Write the equation for the
- Summer 2023, AS Unit 2, Q3 (1 mark): Name the reagent that is needed to change unsaturated oils into saturated fats. [1]
- Summer 2023, AS Unit 2, Q5 (2 marks): Propene reacts with hydrogen bromide. C3H6 HBr C3H7Br + Draw the structures of the two isomers formed and give the name of the major product. [2] Major product
- Summer 2023, AS Unit 2, Q7 (2 marks): Name the following E-Z isomer. [2] H CH2 CH3 C C H3C CH2 Br
- Summer 2022, Unit 4, Q2 (1 mark): Give the name of a compound of formula C4H8 that will decolourise acidified potassium manganate(VII). [1]
- Summer 2022, Unit 4, Q9(d)(ii) (1 mark): During this reaction a cumene radical is produced. State what is meant by the term ‘radical’. [1]
- Summer 2022, Unit 4, Q9(d)(iii) (1 mark): Give the formula of a radical formed during the reaction of methane with chlorine. [1]
- Summer 2022, Unit 4, Q12(b)(i) (1 mark): In the first stage of this method bromine adds across the C C double bonds present. State the type of mechanism occurring when bromine adds across these double
- Summer 2022, AS Unit 2, Q1(a)(i) (1 mark): State the expected colour change for a positive test for alkenes. [1]
- Summer 2022, AS Unit 2, Q1(a)(ii) (1 mark): Draw the structure of the product formed when propene reacts with bromine water. [1]
- Summer 2022, AS Unit 2, Q1(b) (1 mark): Identify another reagent that can be used to test for the presence of alkenes. [1]
- Summer 2022, AS Unit 2, Q2(a) (1 mark): Draw an s-orbital and a p-orbital in the space below. [1]
- Summer 2022, AS Unit 2, Q2(b) (1 mark): Name the type of bond shown in the diagram below. [1] H C C H
- Summer 2022, AS Unit 2, Q4 (1 mark): Complete the equation below to show the product of addition polymerisation. [1] W X n C C Y Z
- Summer 2022, AS Unit 2, Q7(b)(i) (2 marks): Write an equation for the complete combustion of hexane in excess oxygen. [2]
- Summer 2022, AS Unit 2, Q7(b)(iii) (1 mark): 2,2-dimethylbutane is the isomer of C6H14 which ignites most readily. Suggest a reason for this. [1]
- Summer 2019, Unit 4, Q8(a)(i) (1 mark): This reaction involves radicals. In the first stage chlorine radicals are formed. They then attack the ethanoic acid molecule producing a molecule of hydrogen c
- Summer 2019, Unit 4, Q9(a)(i) (1 mark): Explain what can be deduced about the structural formula of alkene T. [1]
- Summer 2019, Unit 4, Q9(a)(iv) (2 marks): Use your answer to part (iii) and other relevant information given in the question to give the structure of alkene T. Name alkene T. [2] Name
- Summer 2019, AS Unit 2, Q3 (2 marks): The compounds shown below have the same molecular formula. H3C H H3C CH3 C C C C H3C H H H A B State which of these compounds can exist as E-Z isomers. Explain
- Summer 2019, AS Unit 2, Q5(a) (1 mark): State the type of polymerisation involved when 2-fluorobut-2-ene, CH3CF CHCH3, — forms a polymer. [1]
- Summer 2019, AS Unit 2, Q5(b) (1 mark): Draw one repeat unit of the polymer formed when 2-fluorobut-2-ene is polymerised. [1]
- Summer 2018, Unit 4, Q8(a) (1 mark): For a number of years CFCs were used in refrigeration and in air conditioning. The use of these compounds is in decline as they damage the ozone layer. A typica
- Summer 2018, Unit 4, Q8(d)(ii) (2 marks): The addition of hydrogen bromide to 1,3,3,3-tetrafluoropropene results in two structural isomers, each of molecular formula C3H3BrF4. I. State the type of mecha
- Summer 2018, AS Unit 2, Q4 (1 mark): Complete the diagram to show the formation of the π-bond in ethene. [1] H H H H C C C C H H H H
- Summer 2018, AS Unit 2, Q6 (1 mark): Draw two repeat units for the polymer formed from the monomer pent-2-ene. [1]
- Summer 2018, AS Unit 2, Q7 (2 marks): Draw diagrams to show the structures of the E and Z isomers of 2-bromopent-2-ene. Label the isomers E and Z. [2]
- Summer 2018, AS Unit 2, Q8(b) (4 marks): State why it is necessary to use ultraviolet light when making chloroethane from ethane. Give equations to show the mechanism for the formation of chloroethane.
- Summer 2018, AS Unit 2, Q8(c) (3 marks): The student found that he had made 1.0 g of chloroethane. Calculate his percentage yield. [3] Percentage yield = %
- Summer 2018, AS Unit 2, Q8(d) (2 marks): The student was disappointed by the yield he obtained but his teacher told him that the yield was always poor due to other products being formed in this reactio
- Summer 2018, AS Unit 2, Q9(d) (1 mark): Suggest the type of reaction that occurs between ethyne and hydrogen. [1]
- Summer 2018, AS Unit 2, Q13(b)(i) (1 mark): of the unknown alkane in terms of x and y. [1] Volume carbon dioxide = cm3 Volume water vapour = cm3
- Summer 2018, AS Unit 2, Q13(b)(ii) (2 marks): [2] y =
- Summer 2017, Unit 4, Q13(a)(ii) (3 marks): Another student suggested that the compound was bromocyclobutane. Br I. Describe a chemical test that would show that the compound was either L, M or N and not
- Summer 2017, Unit 4, Q13(c)(i) (2 marks): The bromination of 4-bromomethylbenzene is a free radical process. Give the equation for this reaction and then use the equation to calculate the minimum mass o
- Summer 2017, AS Unit 2, Q4 (1 mark): A section of polymer is shown. CH3 Cl CH3 H C C C C H H H Cl Draw the structural formula of the monomer used to make this polymer. [1]
- Summer 2017, AS Unit 2, Q8(a)(i) (3 marks): Find the empirical formula of X and hence its molecular formula. Show clearly how you carried out your calculation. [3] Molecular formula
- Summer 2017, AS Unit 2, Q8(a)(ii) (2 marks): Explain what can be deduced from the fact that 11.2 g of X reacts with exactly 32.0 g of bromine. [2]
- Summer 2017, AS Unit 2, Q8(a)(iii) (1 mark): What type of reaction mechanism occurs when X reacts with bromine in the absence of light? [1]
- Summer 2017, AS Unit 2, Q8(a)(iv) (1 mark): What type of reaction mechanism occurs when X reacts with more bromine in the presence of sunlight? [1]
- Summer 2017, AS Unit 2, Q8(a)(v) (3 marks): Draw displayed formulae for each of the following. [3] Compound X The product formed when X reacts with bromine in the absence of light One possible product for
- Summer 2016, AS Unit 2, Q3 (1 mark): Draw a section of the addition polymer formed from the monomer below. CH3CH(OH)CH CHCl You should show two repeat units. [1]
- Summer 2016, AS Unit 2, Q5(a) (1 mark): State what feature of a molecule gives rise to E-Z isomerism. [1]
- Summer 2016, AS Unit 2, Q5(b) (1 mark): Does the molecule shown below show E-Z isomerism? Explain your answer. [1] CH3CH2CH C(CH3)2
- Summer 2016, AS Unit 2, Q9(a) (5 marks): Describe the bonding in propene and use this to explain its reactivity. [5]
- Summer 2016, AS Unit 2, Q9(b) (4 marks): Draw the mechanism for the reaction between propene and bromine. You should show any relevant dipoles, lone pairs of electrons and curly arrows to indicate the
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