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ChemistryCarboxylic acid and their DerivativesPREPARATION OF CARBOXYLIC ACIDS AND THEIR DERIVATIVESMedium2 minQB
ChemistryMediumsingle choice

The compound which undergo nucelophilic substitution fastest would be :

Options:

Answer:
C
Solution:

Question Explanation:

The question asks which of the given acyl compounds undergoes nucleophilic substitution at the fastest rate.

Concept:

This question is based on the reactivity order of carboxylic acid derivatives.

Solution:  

The rate of nucleophilic substitution depends on the electrophilicity of the carbonyl carbon and the leaving group ability.

Acid halides (–COCl) are the most reactive acyl derivatives because chlorine has a strong –I effect, increasing the positive character of the carbonyl carbon.

Additionally, Cl- is a good leaving group, facilitating rapid substitution.

General reactivity order: Acid halide > Anhydride > Ester > Amide. Ketones do not undergo nucleophilic substitution reaction.

Stream:JEESubject:ChemistryTopic:Carboxylic acid and their DerivativesSubtopic:PREPARATION OF CARBOXYLIC ACIDS AND THEIR DERIVATIVES
2mℹ️ Source: QB

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