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- Recrystallisation of Benzoic Acid and Determination of its Melting Point Simplified Revision Notes

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7.1 - Recrystallisation of Benzoic Acid and Determination of its Melting Point

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Experiment Summary

This experiment involves purifying a sample of impure benzoic acid by recrystallisation and then determining the melting point of the purified sample.

  • Recrystallisation involves dissolving the impure solid in a hot solvent and filtering out insoluble impurities.
  • As the solution cools, pure crystals of benzoic acid form and can be collected.
  • The melting point of the recrystallised benzoic acid is measured and compared to the melting point of a pure sample to assess the purity of the recrystallised product.

Materials and Apparatus Required

Chemicals

  • Impure benzoic acid (1 g sample)
  • Deionised water (boiling)
  • Ice-cold deionised water

Apparatus

  • 100 cmÂł and 250 cmÂł beakers
  • 250 cmÂł conical flask
  • Oven set at 100°C
  • Filter funnel and filter paper
  • Hirsch or Buchner funnel
  • Small Buchner flask
  • Rubber adaptor
  • Retort stand, clamp, and boss head
  • Hotplate or Bunsen burner with tripod and gauze
  • Spatula
  • Clock glass
  • Safety glasses
  • Heat-resistant gloves
  • Melting point tubes
  • Mortar and pestle
  • Thiele tube or oil bath for melting point determination
  • Thermometer (-10°C to 150°C)

Safety Precautions

  • Wear safety glasses throughout the experiment.
  • Benzoic acid may irritate the skin and eyes; avoid direct contact.
  • Use heat-resistant gloves when handling hot glassware or working near the hotplate.
  • Avoid burns when handling hot equipment or solvents.
  • Be cautious when heating liquid paraffin for melting point determination, as it can ignite at high temperatures.

Method

Recrystallisation of Benzoic Acid

  1. Boil approximately 100 cmÂł of deionised water and keep it at a constant boil.
  2. Weigh about 1 g of impure benzoic acid and place it in a 100 cmÂł beaker.
  3. Add 25 cmÂł of boiling water to the beaker containing benzoic acid and stir the mixture while heating gently until the benzoic acid dissolves.
  4. If needed, add small amounts of boiling water to dissolve any remaining crystals, using the minimum amount necessary.
  5. Prepare a hot filtration setup with a filter funnel and fluted filter paper in a conical flask containing 20 cmÂł of boiling water.
  6. Pour the hot benzoic acid solution through the filter to remove insoluble impurities.
  7. Transfer the filtrate to a warm 100 cmÂł beaker and heat until crystals start to form on the sides of the beaker.
  8. Then allow the solution to cool to room temperature.
  9. Once cooled, further cool the solution in an ice bath to maximise crystal formation.
  10. Filter the recrystallised benzoic acid using vacuum filtration and wash the crystals with 2 cmÂł of ice-cold deionised water.
  11. Dry the crystals on a clock glass in an oven at 80°C or place them on a radiator for 24 hours.

Determination of Melting Point

  1. Grind a small amount of the recrystallised benzoic acid using a mortar and pestle.
  2. Fill a melting point tube with about 3–5 mm of the crystals.
  3. Attach the tube to a thermometer using a rubber band and place it in a Thiele tube filled with liquid paraffin or an oil bath.
  4. Heat the tube slowly and observe the temperature at which the crystals begin to melt and when they are fully liquefied.
  5. Record this melting point range.
  6. Repeat the process using a sample of pure benzoic acid for comparison.

Results

SubstanceMelting Point Range (°C)
Impure benzoic acid118–121°C
Recrystallised benzoic acid121–123°C
Pure benzoic acid (Analar grade)121–123°C

Example Questions with Answers

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Q1: Why is it important to use the minimum amount of hot solvent during recrystallisation?

Using the minimum amount of solvent ensures that fewer impurities remain dissolved in the solvent, resulting in a higher yield of purified crystals.

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Q2: What should you do if crystals form in the funnel during hot filtration?

Add a small amount of boiling water to the funnel to dissolve the crystals and prevent them from obstructing the filtration process.

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Q3: How could a second crop of crystals be obtained after the first filtration?

Reheat the filtrate to reduce its volume by half, cool it again to room temperature and in an ice bath, and filter the new crystals.

These crystals may not be as pure as the first crop due to the higher concentration of impurities in the remaining solution.

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Q4: How does the melting point of a substance indicate its purity?

A pure substance has a sharp, narrow melting point range.

An impure substance has a lower and broader melting point range due to the presence of impurities that disrupt the crystal structure.

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Q5: What is expected to happen to the melting point when two different pure substances with the same melting point are mixed?

The mixture will lower the melting point and broaden the melting range, as the two different substances act as impurities in each other.

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