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What's in a Medicine?

The iron(III) chloride test and esterifying a phenol

  • 1 thing to know
  • Components 01, 02 and 03

Overview

Recall questions on the neutral iron(III) chloride test, and why a phenol needs an anhydride or acyl chloride rather than a carboxylic acid.

What you need to know

Answer each one before you reveal it.

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Key term

Which reagent converts a phenol into an ester, why can a carboxylic acid not do it directly, and what is formed from phenol and ethanoic anhydride?

Questions from this subtopic

Each one with the model answer underneath.

  1. 1

    Explain why a carboxylic acid is a stronger acid than a phenol.

    Model answer

    The carboxylate ion spreads its negative charge over two equivalent oxygen atoms, which stabilises it more effectively than delocalisation into a benzene ring.

  2. 2

    State the reagent used as the standard chemical test for a phenol.

    Model answer

    Neutral iron(III) chloride solution is used.

  3. 3

    What is a positive result for the iron(III) chloride test?

    Model answer

    A purple colouration develops.

  4. 4

    Why must the iron(III) chloride solution be neutral for this test?

    Model answer

    Acidic conditions suppress the ionisation of the phenol, so the coloured complex does not form reliably.

  5. 5

    A compound gives a purple colour with neutral iron(III) chloride solution but no effervescence with sodium carbonate. Which functional group is present?

    Model answer

    A phenol group is present.

  6. 6

    Which reagent converts a phenol into an ester?

    Model answer

    An acid anhydride converts a phenol into an ester.

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