Aspirin Synthesis,Acylation mechanism and Acylchlorides,

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12 Terms

1
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Give 2 chemicals that can react with salicylic acid that creates Aspirin

Ethanoic anhydride Or Acyl chloride

2
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Suggest 3 reasons why ethanoic anhydride is used instead of acyl chloride

Using acylchloride will produce a corrosive gas as a byproduct

Less expensive

Less reactive so it’s easier to control the rate of reaction

3
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Why is phosphoric acid used in Aspirin synthesis?

To be a catalyst

4
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Suggest why water is added in Aspirin Synthesis

It will hydrolyse any remaining reactants, to remove impurities.

5
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Explain why air is sucked through the apparatus for 5 minutes

To dry the product and remove all the water or solvent

6
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What are the steps to name an Acylchloride?

  1. Count the number of Carbons in the R group

  2. Add the suffix -oyl chloride

  3. If it is branched count from the Acyl functional group to assign its number, place it at the front

7
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Draw the mechanism of the adulation of ethanoylchloride and Ammonia and name the products formed

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8
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Draw the fully displayed structure of 2methylbutanoylchloride

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9
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<p>Name this compound</p>

Name this compound

Ethanoyl Chloride

10
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<p>Name this compound</p>

Name this compound

Butanoyl chloride

11
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If ethanoyl chloride reacts with ammonia what are the products produced?

Ethanamide and HCL in the gaseous state and is corrosive

12
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Why are acylchlorides so reactive?

Because of the polarity of the chlorine and the oxygen. Causing the carbon to become very positive making it susceptible to attack.