A Level Chemistry 9701, topic 33

Carboxylic acids and derivatives: past paper questions

24 Cambridge A Level Chemistry 9701 questions on Carboxylic acids and derivatives (33) from 16 papers, 2023 to 2026. Open the paper or try a question free.

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Questions
24
Papers
16
Years
2023 to 2026
Total marks
287
Average per question
12 marks
Largest question
16 marks

By type: Structured 24

How hard the questions are

  • Recall0
  • Apply2
  • Analyse22
  • Not banded0

Derived from the command word Cambridge prints in each question, banded by a fixed table beside the syllabus's own definitions. A question printing no command word is unbanded: unknown, not middling.

Command words

  • completeApply20 questions
  • drawApply19 questions
  • suggestAnalyse17 questions

    apply knowledge and understanding to situations where there are a range of valid responses in order to make proposals / put forward considerations

  • explainAnalyse14 questions

    set out purposes or reasons / make the relationships between things evident / provide why and/or how and support with relevant evidence

  • stateRecall9 questions

    express in clear terms

  • giveRecall8 questions

    produce an answer from a given source or recall/memory

  • identifyRecall8 questions

    name/select/recognise

  • nameRecall7 questions
  • writeRecall7 questions
  • calculateApply4 questions

    work out from given facts, figures or information

Where the questions come from

By year

  • 20264
  • 20258
  • 20247
  • 20235

By session

  • May/June13
  • Oct/Nov11

By paper

  • Paper 424

Questions on this topic

Showing 14 of 24, spread across the years. Open one to write your answer and have it marked.

  • Question 2May/June 2026, paper 41Structured11 marks

    Define pH mathematically.

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  • Question 7Oct/Nov 2025, paper 41Structured12 marksHas a diagram

    State the relative acidities of bromoethanoic acid, BrCH2COOH, chloroethanoic acid, ClCH2COOH, ethanoic acid, CH3COOH and ethanol, CH3CH2OH.

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  • Question 7Oct/Nov 2024, paper 41Structured15 marksHas a diagram

    A reaction scheme is shown in Fig. 7.1. The reagents needed for reaction 2 and reaction 3 are stated. Reaction 5 takes place when C2H5NH2 is mixed with compound V.

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  • Question 9Oct/Nov 2023, paper 41Structured13 marksHas a diagram

    Benzoyl chloride, C6H5COCl, can be made from ethyl benzene in a two-step process. A reaction scheme is shown. Draw the intermediate organic compound M in the box.

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  • Question 8May/June 2026, paper 41Structured10 marksHas a diagram

    Secondary amine M can be made by the three-step synthesis shown in Figure 8.1. Write an equation for the reaction of CH3COOH with SOCl2 in step 1.

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  • Question 8Oct/Nov 2025, paper 41Structured13 marksHas a diagram

    In the electrophilic substitution of arenes, different substituents can direct to different ring positions. Describe the directing effect of the −NO2 group.

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  • Question 6Oct/Nov 2024, paper 42Structured12 marksHas a diagram

    Fig. 6.1 shows two reactions of ethanedioic acid, HOOCCOOH. Draw the organic product G in the box in Fig. 6.1.

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  • Question 7Oct/Nov 2023, paper 42Structured11 marksHas a diagram

    Benzene can be used to make benzoic acid in the two-step process shown in Fig. 7.1. Fig. 7.1 Give the reagents and conditions for step 1 and step 2.

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  • Question 9Oct/Nov 2023, paper 42Structured14 marksHas a diagram

    State the reactants and conditions for two different types of reactions that both produce diethylamine, CH3CH2NHCH2CH3.

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  • Question 7May/June 2025, paper 41Structured11 marksHas a diagram

    A hydrocarbon is known to be either compound D or compound E. Give the systematic name of E.

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  • Question 8May/June 2024, paper 42Structured16 marksHas a diagram

    State the relative basicities of phenylamine, C6H5NH2, benzylamine, C6H5CH2NH2, and ammonia, NH3, in aqueous solution.

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  • Question 5May/June 2023, paper 42Structured14 marksHas a diagram

    Methylbenzene can undergo different reactions, as shown in Fig. 5.1. Draw structures in Fig. 5.1 for the possible organic products of the three reactions shown.

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  • Question 10May/June 2025, paper 41Structured7 marks

    Propanoic acid, methanoic acid and ethanedioic acid are all weak acids. Draw the displayed formula of ethanedioic acid.

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  • Question 9May/June 2024, paper 42Structured12 marksHas a diagram

    Explain why trichloroethanoic acid, CCl3COOH, is more acidic than ethanoic acid, CH3COOH.

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