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.
Practising builds a set from this topic, free with an account. One question opens straight away, with no account.
- 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.
- Try this questionQuestion 2May/June 2026, paper 41Structured11 marks
Define mathematically.
- Try this questionQuestion 7Oct/Nov 2025, paper 41Structured12 marksHas a diagram
State the relative acidities of bromoethanoic acid, , chloroethanoic acid, , ethanoic acid, and ethanol, .
- Try this questionQuestion 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 is mixed with compound .
- Try this questionQuestion 9Oct/Nov 2023, paper 41Structured13 marksHas a diagram
Benzoyl chloride, , can be made from ethyl benzene in a two-step process. A reaction scheme is shown. Draw the intermediate organic compound in the box.
- Try this questionQuestion 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 with in step 1.
- Try this questionQuestion 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 group.
- Try this questionQuestion 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.
- Try this questionQuestion 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.
- Try this questionQuestion 9Oct/Nov 2023, paper 42Structured14 marksHas a diagram
State the reactants and conditions for two different types of reactions that both produce diethylamine, .
- Try this questionQuestion 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.
- Try this questionQuestion 8May/June 2024, paper 42Structured16 marksHas a diagram
State the relative basicities of phenylamine, , benzylamine, , and ammonia, , in aqueous solution.
- Try this questionQuestion 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.
- Try this questionQuestion 10May/June 2025, paper 41Structured7 marks
Propanoic acid, methanoic acid and ethanedioic acid are all weak acids. Draw the displayed formula of ethanedioic acid.
- Try this questionQuestion 9May/June 2024, paper 42Structured12 marksHas a diagram
Explain why trichloroethanoic acid, , is more acidic than ethanoic acid, .






