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Benzic acid can be prepared from ethyl benzoate - AQA - A-Level Chemistry - Question 3 - 2017 - Paper 3

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Benzic acid can be prepared from ethyl benzoate. Ethyl benzoate is first hydrolysed in alkaline conditions as shown: Add 5.0 cm³ of ethyl benzoate (density = 1.... show full transcript

Worked Solution & Example Answer:Benzic acid can be prepared from ethyl benzoate - AQA - A-Level Chemistry - Question 3 - 2017 - Paper 3

Step 1

Suggest how the anti-bumping granules prevent bumping during reflux.

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Answer

The anti-bumping granules provide a large surface area for small bubbles to form, preventing the development of very large bubbles which can lead to bumping.

Step 2

Show, by calculation, that an excess of sodium hydroxide is used in this reaction.

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Answer

The mass of ethyl benzoate used is calculated as follows:

extMassofester=5.0extcm3imes1.05extgcm3=5.25extg ext{Mass of ester} = 5.0 ext{ cm}^3 imes 1.05 ext{ g cm}^{-3} = 5.25 ext{ g}

Using the molar mass of ethyl benzoate (Mr = 150 g/mol), the moles of ethyl benzoate can be calculated:

extAmountofester=5.25extg150extgmol1=0.0350extmol ext{Amount of ester} = \frac{5.25 ext{ g}}{150 ext{ g mol}^{-1}} = 0.0350 ext{ mol}

The amount of sodium hydroxide in 30.0 cm³ of 2 mol dm⁻³ solution is:

extMolesofNaOH=2extmoldm3imes0.030extdm3=0.060extmol ext{Moles of NaOH} = 2 ext{ mol dm}^{-3} imes 0.030 ext{ dm}^3 = 0.060 ext{ mol}

Since 0.060 mol of NaOH is available against 0.0350 mol of ethyl benzoate, there is an excess of sodium hydroxide.

Step 3

Suggest why an excess of sodium hydroxide is used.

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Answer

An excess of sodium hydroxide ensures that all of the ethyl benzoate reacts completely, preventing any unreacted ester from remaining in the mixture.

Step 4

Suggest why an electric heater is used rather than a Bunsen burner in this hydrolysis.

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Answer

An electric heater is used to provide a more even and controlled heating, which reduces the risk of igniting flammable vapors that may be present.

Step 5

State why reflux is used in this hydrolysis.

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Answer

Reflux is used to maintain the reaction mixture at its boiling point for an extended period without losing any volatile components, ensuring thorough hydrolysis of the ester.

Step 6

Write an equation for the reaction between sodium benzoate and hydrochloric acid.

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Answer

The equation for the reaction is:

C6H5COONa+HClC6H5COOH+NaCl\text{C}_6\text{H}_5\text{COONa} + \text{HCl} \rightarrow \text{C}_6\text{H}_5\text{COOH} + \text{NaCl}

Step 7

Suggest why sodium benzoate is soluble in cold water but benzoic acid is insoluble in cold water.

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Answer

Sodium benzoate is soluble in cold water due to its ionic nature and the ability to form interactions with water molecules, while benzoic acid has non-polar characteristics and fewer favorable interactions with water, leading to its insolubility.

Step 8

Describe the method the student should use to purify the benzoic acid.

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Answer

To purify the benzoic acid, the student should:

  1. Dissolve the crude benzoic acid in a minimum volume of hot water to ensure it completely dissolves.
  2. Allow the solution to cool slowly, leading to the crystallization of pure benzoic acid.
  3. Filter the crystals using a Buchner funnel and wash them with cold water to remove impurities.
  4. Dry the purified benzoic acid using filter paper or in a desiccator.

Step 9

Calculate the percentage yield of benzoic acid.

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Answer

Using the provided data, the moles of ethyl benzoate used in the reaction were 0.0400 mol. The theoretical yield of benzoic acid can be calculated based on the stoichiometry (1:1 ratio) of the reaction. Each mole of ethyl benzoate yields one mole of benzoic acid.

The theoretical mass of benzoic acid produced is:

extTheoreticalmass=0.0400extmolimes122.12extgmol1=4.88extg ext{Theoretical mass} = 0.0400 ext{ mol} imes 122.12 ext{ g mol}^{-1} = 4.88 ext{ g}

The actual mass obtained was 5.12 g. Hence,

ext{Percentage yield} = \left( \frac{5.12 ext{ g}}{4.88 ext{ g}} \right) \times 100 = 104.9\%$$

Step 10

Suggest why the yield is not 100%.

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Answer

The yield may not be 100% due to several factors:

  1. Loss of product during transfer or filtration.
  2. Incomplete reaction if all ethyl benzoate did not convert to benzoic acid.
  3. Impurities remaining in the product might contribute to a higher measured mass.

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