Answered

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(a) Prop-2-en-1-ol can be prepared by reacting 3-chloroprop-1-ene with dilute aqueous sodium
hydroxide. Name the mechanism for this reaction.

Sagot :

GinnyAnswer

Final answer:

The mechanism for the formation of Prop-2-en-1-ol from 3-chloroprop-1-ene involves nucleophilic trapping.


Explanation:

The mechanism for the reaction of 3-chloroprop-1-ene with dilute aqueous sodium hydroxide to produce Prop-2-en-1-ol involves nucleophilic trapping. This mechanism consists of the nucleophilic attack of the hydroxide ion on the electrophilic center, leading to the formation of the final product.


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