Phenol, C6H5OH, is a weak acid.
- (a)Phenol can be made from phenylamine, C6H5NH2. Give the reagents and conditions for this reaction.[2]
- (b)Phenol reacts with dilute aqueous nitric acid under room conditions to give a mixture of two isomeric products with molecular formula C6H5NO3. Use the Data Booklet to draw the structural formulae of these two products in the boxes and name each product. [Figure shows two empty boxes labelled 'name'][2]
- (c)(i)Phenol reacts with an excess of aqueous bromine. Draw and name the organic product of this reaction in the box. [Figure shows an empty box labelled 'name'][2]
- (c)(ii)Describe two visual observations that can be made when phenol reacts with an excess of aqueous bromine.[1]
- (d)Write an equation for a neutralisation reaction in which phenol behaves as an acid.[1]
- (e)Water, phenol and ethanol can all behave as acids. Place these three compounds in order of acidity, starting with the most acidic. Explain your answer.[3]
This question uses a diagram from the original paper, which isn't shown here. Open the full paper from the past papers archive to see it.
Mark scheme
Marking points from the official mark scheme (Oct/Nov 2020). The mark or mark type is shown in brackets.
- [1] M1: HNO2 OR NaNO2 + HCl
- [1] M2: T ≥ 10 °C / warm AND water
- [1] (b) Structure for 2-nitrophenol
- [1] (b) Name: 2-nitrophenol
- [1] (b) Structure for 4-nitrophenol
- [1] (b) Name: 4-nitrophenol
- [1] (c)(i) Structure for 2,4,6-tribromophenol
- [1] (c)(i) Name: 2,4,6-tribromophenol
- [1] bromine is decolourised AND white precipitate is formed BOTH
- [1] C6H5OH + NaOH → C6H5ONa + H2O ALLOW any equation for phenol acting as an acid
- [1] phenol>water>ethanol
- [1] (explanation) (phenol:) lone pair on oxygen is delocalised into the benzene ring
- [1] (explanation) (ethanol:) positive inductive effect / electron donating effect of alkyl / ethyl group
- [1] (explanation) correct statement about stabilisation of anion/ conjugate base OR weakening of O-H bonds once in the context of phenol / ethanol
- [1] (explanation) correct statement about ease of proton/H+ donation in the context of phenol / ethanol (Two correct statements = 1 mark)
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