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Phenol and bromine water: Edexcel International A Level Chemistry questions

Edexcel International A Level Chemistry past-paper questions on 18.1.4 Phenol and bromine water, 2019–2025, with mark schemes and examiner’s reports where available.

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  1. Q20(d)(iii)

    June 2025 · Unit 5

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  2. Q13

    June 2025 (A) · Unit 5

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  3. Q22

    January 2025 · Unit 5

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  4. Q2(a)

    January 2025 · Unit 6

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  5. Q15(a)(iii)

    June 2024 · Unit 5

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  6. Q14(e)

    January 2024 · Unit 5

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  7. Q20(a)(ii)

    October 2023 · Unit 5

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  8. Q16

    June 2023 · Unit 5

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  9. The start of question 19

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  10. Q19(a)(ii)

    January 2023 · Unit 5

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  11. Q20

    October 2022 · Unit 5

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  12. Q11

    June 2022 · Unit 5

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  13. Q12

    October 2021 · Unit 5

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  14. Q20(c)(i)

    June 2021 · Unit 5

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  15. Q20(c)(ii)

    June 2021 · Unit 5

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All 15 questions on Phenol and bromine water, as a list
  1. June 2025, Unit 5, Q20(d)(iii) (3 marks): Explain why benzenecarboxylic acid requires concentrated nitric and sulfuric acids for nitration while salicylic acid may be nitrated using dilute nitric acid.
  2. June 2025 (A), Unit 5, Q13 (1 mark): The reaction between chlorine and phenol is faster than that between chlorine and benzene. Which is the best explanation for this? A the carbon‑oxygen bond is w
  3. January 2025, Unit 5, Q22 (6 marks): * 22 Compare and contrast the bromination of benzene and the bromination of phenol. Include equations in your answer. Detailed mechanisms are not required. (6)
  4. January 2025, Unit 6, Q2(a) (2 marks): A student suggested using iron as a catalyst in Step 1. Explain why it is not needed in the reaction with phenol, even though chlorination of other aryl compoun
  5. June 2024, Unit 5, Q15(a)(iii) (3 marks): Explain why the reaction of chlorine with phenol occurs under milder conditions than the reaction of chlorine with benzene. (3)
  6. January 2024, Unit 5, Q14(e) (2 marks): Another painkiller, paracetamol, can be synthesised from phenol in a similar sequence. Phenol is nitrated by dilute nitric acid. H NO2 NH2 N O HO HO HO HO pheno
  7. October 2023, Unit 5, Q20(a)(ii) (6 marks): Compare and contrast the reaction of benzene with bromine with the reactions of cyclohexene with bromine and of phenol with bromine. Include reasons for any dif
  8. June 2023, Unit 5, Q16 (1 mark): Which statement explains why bromine reacts more readily with phenol than with benzene? A the O H bond in phenol is polar B the oxygen atom in phenol is very el
  9. January 2023, Unit 5, Q19(a)(i) (3 marks): Draw a mechanism for the reaction to form 2-nitrophenol. + is the electrophile. Assume that NO2 (3)
  10. January 2023, Unit 5, Q19(a)(ii) (2 marks): Benzene requires a mixture of concentrated nitric acid and concentrated sulfuric acid at 60 °C to form nitrobenzene. Explain why phenol requires milder conditio
  11. October 2022, Unit 5, Q20 (6 marks): *20 Delocalised electron systems are important in determining the chemical properties of some compounds. Compare and contrast the chemical reactions of bromine
  12. June 2022, Unit 5, Q11 (1 mark): Which is correct for the reaction of bromine with phenol when compared with benzene? Reactivity of phenol Electron density of the ring in phenol A more reactive
  13. October 2021, Unit 5, Q12 (1 mark): What is the molar mass, in g mol–1, of the organic product when phenol reacts with excess bromine water? A 156.9 B 172.9 C 330.7 D 488.5
  14. June 2021, Unit 5, Q20(c)(i) (1 mark): Identify, by name or formula, the organic product when phenol reacts with excess bromine. (1)
  15. June 2021, Unit 5, Q20(c)(ii) (2 marks): Explain why bromine reacts much faster with phenol than with benzene. (2)

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