Answer and Explanation:
In the acyl substitution reaction, aldehydes and ketones which have a carbonyl group in their structure, are not left with any leaving group during the reaction.
And hence, the product is not formed.
For steric and electrical reasons, aldehydes are more reactive than ketones in nucleophilic addition processes.
In ketones, the presence of two relatively big substituents makes it more difficult for a nucleophile to access the carbonyl carbon than in aldehydes with only one such substituent.
Many aldehydes and ketones undergo substitution reactions at alpha carbons.
These reactions are acid or base catalyzed, but in the case of halogenation the reaction generates an acid as one of the products, and is therefore autocatalytic.
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introduce the various classes of carbonyl compounds Nucleophilic acyl substitution reactions primarily occur when the carbonyl compound is an acid amide but an intermediate ion that undergoes further reaction as we showed in Figure |
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Carbonyl compounds compounds containing carbonyl groups aldehydes and ketones do not have leaving groups so cannot undergo substitution reactions Nucleophilic acyl substitution reaction = nucleophile replaces the substituent |
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