Answered

Discover the best answers at Westonci.ca, where experts share their insights and knowledge with you. Our platform provides a seamless experience for finding precise answers from a network of experienced professionals. Experience the ease of finding precise answers to your questions from a knowledgeable community of experts.

Aspirin synthesis involves the addition of an acetyl group to salicylic acid in a condensation reaction with an alcohol. The acetyl group could be added with a carboxylic acid but the preferred procedure is to use the acid anhydride. Why is preferable to use an acid anhydride for ester formation with an alcohol rather than a carboxylic acid

Sagot :

pstnonsonjoku

Answer:

See explanation

Explanation:

The synthesis of asprin involves the;

i) Hydrolysis of Methyl salicylate

ii) Reaction of salicylic acid with acid anhydride

The chemical name of asprin is acetylsalicylic acid.

It is preferable to use an acid anhydride for ester formation with an alcohol rather than a carboxylic acid because we will not produce water which can then cause the hydrolysis of the newly formed ester.

Thank you for your visit. We are dedicated to helping you find the information you need, whenever you need it. Thank you for choosing our platform. We're dedicated to providing the best answers for all your questions. Visit us again. Westonci.ca is here to provide the answers you seek. Return often for more expert solutions.