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Oxidation of alcohols: AQA A‑Level Chemistry questions

AQA A-Level Chemistry past-paper questions on 3.3.5.2 Oxidation of alcohols, 2008–2025, with mark schemes and examiner’s reports where available.

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  1. Q04.2

    June 2025 · Paper 2

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  2. Q05.1

    June 2025 · Paper 3

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  3. Q05.2

    June 2025 · Paper 3

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  4. Q05.3

    June 2025 · Paper 3

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  5. Q11

    June 2025 · AS Paper 2

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  6. Q13

    June 2025 · AS Paper 2

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  7. Q07.1

    June 2024 · AS Paper 2

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  8. Q07.2

    June 2024 · AS Paper 2

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  9. Q13

    June 2024 · AS Paper 2

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  10. Q06.4

    June 2023 · Paper 2

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  11. Q32

    June 2023 · Paper 3

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  12. Q22

    June 2023 · AS Paper 2

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  13. Q24

    June 2022 · Paper 3

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  14. Q15

    June 2022 · AS Paper 2

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  15. Q06.1

    November 2021 · Paper 3

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  16. Q06.2

    November 2021 · Paper 3

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  17. Q06.3

    November 2021 · Paper 3

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  18. Q06.4

    November 2021 · Paper 3

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  20. Q26

    November 2021 · Paper 3

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All 73 questions on Oxidation of alcohols, as a list
  1. June 2025, Paper 2, Q04.2 (1 mark): Deduce the role of the concentrated nitric acid in the reaction. [1 mark]
  2. June 2025, Paper 3, Q05.1 (6 marks): A student has separate unlabelled samples of propan-1-ol and propan-2-ol but does not know which sample is which alcohol. The student plans a series of steps to
  3. June 2025, Paper 3, Q05.2 (3 marks): A primary alcohol can be oxidised to form a carboxylic acid using an excess of the oxidising agent in Question 05.1. Give the condition needed for this reaction
  4. June 2025, Paper 3, Q05.3 (1 mark): During oxidation reactions, anti-bumping granules are often added to the pear-shaped flask containing the reactants. State why anti-bumping granules are used. [
  5. June 2025, AS Paper 2, Q11 (1 mark): Which compound produces (CH3)2CHCOCH3 on oxidation? [1 mark] A 2-methylpropan-1-ol B 2,2-dimethylpropan-1-ol C 2-methylbutan-2-ol D 3-methylbutan-2-ol
  6. June 2025, AS Paper 2, Q13 (1 mark): 2-Methylpentane-1,2,4-triol is refluxed with an excess of acidified potassium dichromate(VI). What is the molecular formula of the main organic product? [1 mark
  7. June 2024, AS Paper 2, Q07.1 (1 mark): Acidified potassium dichromate(VI) is used as the oxidising agent. State the colour change in this reaction. [1 mark]
  8. June 2024, AS Paper 2, Q07.2 (1 mark): A second organic product, X, is formed in small quantities. The boiling point of X is 49 °C Identify X. [1 mark]
  9. June 2024, AS Paper 2, Q13 (1 mark): Which diagram shows the correct apparatus for the conversion of hexan-1-ol to hexanal? [1 mark] A B C D
  10. June 2023, Paper 2, Q06.4 (3 marks): Figure 10 shows the apparatus that is used to separate a mixture of liquids K and M using fractional distillation. Suggest labels that should be added to positi
  11. June 2023, Paper 3, Q32 (1 mark): Which is a correct equation for the oxidation of 1-phenylethanol? [O] represents oxygen from an oxidising agent. [1 mark] A C6H5CH2CH2OH + 2 [O] → C6H5CH2COOH +
  12. June 2023, AS Paper 2, Q22 (1 mark): The alcohol CH3CH2CH2OH can be oxidised. Which compound cannot be produced by oxidation of this alcohol? [1 mark] A CO2 B CH3COCH3 C CH3CH2CHO D CH3CH2COOH
  13. June 2022, Paper 3, Q24 (1 mark): Which statement is not correct for both primary and secondary alcohols? [1 mark] A They are easily oxidised to carboxylic acids by acidified K2Cr2O7 solution. B
  14. June 2022, AS Paper 2, Q15 (1 mark): Which compound produces (CH3)2CHCOCH3 when oxidised? [1 mark] A 2-methylpropan-1-ol B 2,2-dimethylpropanol C 2-methylbutan-2-ol D 3-methylbutan-2-ol
  15. November 2021, Paper 3, Q06.1 (2 marks): Give two reasons why the apparatus shown in Figure 4 is not safe. [2 marks] 1 2
  16. November 2021, Paper 3, Q06.2 (1 mark): Give one additional reagent that is needed to form any propanoic acid. [1 mark]
  17. November 2021, Paper 3, Q06.3 (2 marks): State two more mistakes in the way the apparatus is set up in Figure 4. [2 marks] 1 2
  18. November 2021, Paper 3, Q06.4 (1 mark): State the purpose of the small glass beads in the flask in Figure 4. [1 mark]
  19. November 2021, Paper 3, Q06.5 (4 marks): After correcting the mistakes, the student heats a reaction mixture containing 6.50 g of propan-1-ol with an excess of the oxidising agent. The propanoic acid s
  20. November 2021, Paper 3, Q26 (1 mark): Which compound is produced when 1-phenylethanol reacts with acidified potassium dichromate(VI)? [1 mark] A C6H5CH2CH2OH B C6H5CH2CHO C C6H5COCH3 D C6H5CH(OH)CH3
  21. November 2021, AS Paper 2, Q03.1 (6 marks): Figure 2 shows the apparatus set up by a student to make propanone by this method. Suitable clamps are used to hold all the apparatus firmly in place. Figure 2
  22. November 2020, Paper 2, Q03.1 (2 marks): Identify the isomer(s) that would react when warmed with acidified potassium dichromate(VI). State the expected observation when acidified potassium dichromate(
  23. November 2020, Paper 2, Q03.2 (2 marks): Identify the isomer(s) that would react with Tollens’ reagent. State the expected observation when Tollens’ reagent reacts. [2 marks] Isomer(s) Expected observa
  24. November 2020, Paper 3, Q25 (1 mark): Which compound reacts to form a ketone when warmed with an acidified solution of potassium dichromate(VI)? [1 mark] A CH3CH2CH2OH B (CH3)2CHOH C CH3CH2CHO D (CH
  25. November 2020, AS Paper 2, Q07.2 (2 marks): Ethanedioic acid is formed by the oxidation of ethane-1,2-diol (HOCH2CH2OH). State suitable reagent(s) and a condition for this reaction. [2 marks] Reagent(s) C
  26. June 2019, Paper 2, Q06.1 (3 marks): Give a reagent and observations for a test-tube reaction to distinguish between 2-methylbutan-1-ol and 2-methylbutan-2-ol. [3 marks] Reagent Observation with 2-
  27. June 2019, Paper 2, Q13.2 (2 marks): A student attempted to reduce a sample of 2-methylbutanal but added insufficient NaBH4 The student confirmed that the reduction was incomplete by using a chemic
  28. June 2019, Paper 3, Q22 (1 mark): Which compound is formed when 1-phenylethanol reacts with acidified potassium dichromate(VI)? [1 mark] A C6H5CH2CH2OH B C6H5CH2CHO C C6H5COCH3 D C6H5CH2COOH
  29. June 2019, AS Paper 2, Q08.1 (3 marks): Calculate the minimum volume, in cm3, of 0.40 mol dm–3 potassium dichromate(VI) solution needed to oxidise 6.0 cm3 of propan-1-ol to propanal. Mr of propan-1-ol
  30. June 2019, AS Paper 2, Q08.2 (3 marks): The reaction is done in a pear-shaped flask. Complete the diagram to show the assembled apparatus needed to prepare propanal from propan-1-ol in this way. Label
  31. June 2019, AS Paper 2, Q18 (1 mark): Which compound can be oxidised to form (CH3)2CHCOCH3? [1 mark] A 2-methylpropan-1-ol B 2,2-dimethylpropanol C 2-methylbutan-2-ol D 3-methylbutan-2-ol
  32. June 2018, Paper 2, Q03.1 (3 marks): Explain, with reference to intermolecular forces, why distillation allows propanal to be separated from the other organic compounds in this reaction mixture. [3
  33. June 2018, Paper 2, Q03.2 (2 marks): Give two ways of maximising the yield of propanal obtained by distillation of the reaction mixture. [2 marks] 1 2
  34. June 2018, Paper 3, Q11 (1 mark): Which statement is correct about both 2-methylbutan-1-ol and 2-methylbutan-2-ol? [1 mark] A They can be formed by alkaline hydrolysis of esters. B They can be o
  35. June 2017, Paper 3, Q02.6 (3 marks): A by-product of the reaction of butan-2-ol with concentrated sulfuric acid has the molecular formula C4H8O Name this by-product, identify the role of the sulfur
  36. June 2017, AS Paper 2, Q17 (1 mark): Which alcohol can be oxidised by acidified potassium dichromate(VI) but cannot be dehydrated by heating with concentrated sulfuric acid? [1 mark] A 2,3-dimethyl
  37. June 2016, AS Paper 2, Q06.2 (2 marks): Write an equation for this oxidation reaction of propane-1,2-diol under reflux, using [O] to represent the oxidizing agent. Show the displayed formula of the or
  38. June 2016, AS Paper 2, Q06.3 (2 marks): Draw a labelled diagram to show how you would set up apparatus for refluxing. [2 marks]
  39. June 2016, AS Paper 2, Q06.4 (1 mark): Anti-bumping granules are placed in the flask when refluxing. Suggest why these granules prevent bumping. [1 mark]
  40. June 2016, AS Paper 2, Q06.5 (1 mark): Draw the structure of a different organic product formed when the acidified potassium dichromate(VI) is not in excess. [1 mark]
  41. June 2016, AS Paper 2, Q09 (1 mark): Which of the following compounds would form an orange-red precipitate when heated with Fehling’s solution? [1 mark] A CH3CH2CN B CH3CH2COOH C CH3CHO D CH3COCH3
  42. Specimen, Paper 2, Q04.2 (1 mark): Draw the structure of the organic product, B, formed when A is oxidised in the reaction with acidified potassium dichromate(VI). [1 mark] 0 4 . 2
  43. Specimen, Paper 2, Q04.7 (1 mark): Draw the structure of the isomer of A that is not oxidised by acidified potassium dichromate(VI). [1 mark] 0 4 . 7
  44. Specimen, Paper 3, Q01.1 (3 marks): In order to ensure that the oxidation to ethanoic acid is complete, the reaction is carried out under reflux. Describe what happens when a reaction mixture is r
  45. Specimen, Paper 3, Q01.2 (1 mark): Write a half-equation for the overall oxidation of ethanol into ethanoic acid. [1 mark] 0 1 . 2 3
  46. Specimen, Paper 3, Q01.3 (5 marks): The boiling points of the organic compounds in a reaction mixture are shown in Table 1. Table 1 Compound ethanol ethanal ethanoic acid Boiling point / °C 78 21
  47. June 2016, CHEM2 (old spec), Q4(b) (3 marks): Compounds A and B are both straight-chain compounds. A can be oxidised to form P. B can be oxidised to form Q. P and Q are isomers with molecular formula C4H8O
  48. June 2016, CHEM2 (old spec), Q4(d)(i) (3 marks): Compound S is obtained by distilling it off as it forms during the oxidation. Compound T is formed when the oxidation takes place under reflux. Identify the fun
  49. June 2015, CHEM2 (old spec), Q2(a) (3 marks): Butan-2-ol and 2-methylpropan-2-ol [3 marks] Reagent Observation with butan-2-ol Observation with 2-methylpropan-2-ol
  50. June 2015, CHEM2 (old spec), Q7(b)(i) (1 mark): Write an equation for this reaction using [O] to represent the oxidising agent. [1 mark]
  51. June 2015, CHEM2 (old spec), Q7(b)(ii) (1 mark): State the class of alcohols to which propan-2-ol belongs. [1 mark]
  52. June 2014, CHEM2 (old spec), Q7(d) (1 mark): Two alcohols are formed by the hydration of Isomer 4. Draw the displayed formula for the alcohol formed that is oxidised readily by acidified potassium dichroma
  53. June 2013, CHEM2 (old spec), Q2(d) (3 marks): Butanal and butanone Reagent Observation with butanal Observation with butanone
  54. June 2013, CHEM2 (old spec), Q8(b) (1 mark): Draw the structure of the alcohol with molecular formula C4H10O that is resistant to oxidation by acidified potassium dichromate(VI). (1 mark)
  55. June 2013, CHEM2 (old spec), Q10(d)(ii) (1 mark): Draw the structure of the organic compound with Mr = 60 that is produced in this reaction. (1 mark)
  56. January 2013, CHEM4 (old spec), Q6(a) (3 marks): Reagent Observation with R Observation with S
  57. January 2013, CHEM4 (old spec), Q6(c) (3 marks): Reagent Observation with V Observation with W
  58. January 2013, CHEM2 (old spec), Q5(c)(iv) (2 marks): The earliest breathalysers used laboratory chemicals to oxidise the ethanol to ethanoic acid. Detection was by a colour change. Identify a reagent or combinatio
  59. June 2012, CHEM2 (old spec), Q8(d) (3 marks): State the class of alcohols to which the diol butane-1,4-diol belongs. Identify a suitable reagent or combination of reagents for the conversion of butane-1,4-d
  60. January 2012, CHEM2 (old spec), Q6(b) (2 marks): A simple chemical test, using either Fehling’s solution or Tollens’ reagent, can be used to distinguish between compound 1 and compound 3. Choose one of these t
  61. January 2012, CHEM2 (old spec), Q10(c) (3 marks): Cyclohexanol (B) can be converted into cyclohexanone (C). Give a reagent or combination of reagents that can be used for this reaction and state the type of rea
  62. January 2011, CHEM2 (old spec), Q3(d) (3 marks): Butan-2-ol(l) and 2-methylpropan-2-ol(l) Reagent Observation with butan-2-ol(l) Observation with 2-methylpropan-2-ol(l) (3 marks)
  63. January 2011, CHEM2 (old spec), Q9(a)(iv) (1 mark): Using [O] to represent the oxidising agent, write an equation for the oxidation of butan-1-ol to form an aldehyde. (1 mark)
  64. June 2010, CHEM2 (old spec), Q5(c)(iii) (1 mark): State the class of alcohols to which ethanol belongs. (1 mark)
  65. June 2010, CHEM2 (old spec), Q5(c)(iv) (1 mark): Draw the displayed formula of the carboxylic acid formed when ethanol is oxidised by an excess of acidified potassium dichromate(VI) solution. (1 mark)
  66. January 2010, CHEM2 (old spec), Q9(a) (3 marks): Two of these are butan-l-ol (CH3CH2CH2CH2OH) and butan-2-ol. The other two isomers are alcohol X and alcohol Y. Draw the displayed formula for butan-2-ol. Alcoh
  67. January 2010, CHEM2 (old spec), Q9(d) (5 marks): Butan-l-ol reacts with acidified potassium dichromate(VI) solution to produce two organic compounds. State the class of alcohols to which butan-l-ol belongs. Dr
  68. June 2009, CHEM2 (old spec), Q9(a) (1 mark): 9 (a) State the class of alcohol to which butan-2-ol belongs. (1 mark)
  69. June 2009, CHEM2 (old spec), Q9(c) (1 mark): 9 (c) Draw the displayed formula of the alcohol C4H9OH which is resistant to oxidation by acidified potassium dichromate(VI). (1 mark) Section B Answer both que
  70. June 2008, CHM3W (2008 spec), Q2(e)(i) (1 mark): 2 (e) (i) State the type of reaction. (1 mark)
  71. June 2008, CHM3W (2008 spec), Q2(f)(ii) (1 mark): 2 (f) (ii) Identify the class of alcohol to which prop-2-en-l-ol belongs. (1 mark)
  72. January 2008, CHM3W (2008 spec), Q3(c) (1 mark): (c) State the class of alcohols to which citronellol belongs. (1 mark)
  73. January 2008, CHM3W (2008 spec), Q3(d) (2 marks): (d) Citronellol can be converted into the aldehyde citronellal, which has the following structure. State the type of reaction and a reagent or combination of re

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