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1. Uses of sulphuric acid are as follows:
2. Aspirin is only slightly soluble in water and acidic
solutions because Aspirin contains polar functional groups which
can form hydrogen bonds with polar water molecules. Besides this
Aspirin is a monoprotic weak acid, Ka = 2.8 x
10-4 at 25oC, so very little of the molecular
aspirin (acetylsalicylic acid) dissociates to form acetylsalicylate
ions.
For the equilibrium dissociation reaction:
aspirin (acetylsalicylic acid) | acetylsalicylate ion | + | H+ | |
+ | H+ |
the equilibrium position lies well to the left, favouring molecular
aspirin.
3. The aspirin molecule is made up of a benzene ring, a carboxyl group, and an ester. It has both polar and non-polar components. Thus, the affinity of alcohol molecules for aspirin molecules is relatively similar to the affinity of alcohol molecules for each other. Thus, aspirin is disolves in alcohol.
4.In the synthesis of aspirin you will start with salicylic acid and acetic anhydride Note that it is the -OH group of salicylic acid that reacts with acetic anhydride to form an esterlike product. The carboxylic acid group of salicylic acid remains unchanged. Phosphoric acid will be used as a catalyst in this experiment.
The main impurity in the crystallized aspirin will be salicylic acid, which will co-precipitate with the aspirin if the procedure is done too quickly.