OCR A-Level Chemistry B H433
Development of Practical Skills in Chemistry
Elements of Life
Developing Fuels
Elements From the Sea
The Ozone Story
What's in a Medicine?
The Chemical Industry
Polymers and Life
Oceans
Developing Metals
Colour by Design
Chemical Literacy
Mathematical Skills in Chemistry
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.
Questions from this subtopic
Each one with the model answer underneath.
- 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
State the reagent used as the standard chemical test for a phenol.
Model answer
Neutral iron(III) chloride solution is used.
- 3
What is a positive result for the iron(III) chloride test?
Model answer
A purple colouration develops.
- 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
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
Which reagent converts a phenol into an ester?
Model answer
An acid anhydride converts a phenol into an ester.
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