Aldehydes, Ketones and Carboxylic Acids
Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is
CH3COOCH3
CH3CONH2
CH3COOCOCH3
CH3COCl
D.
CH3COCl
Lesser the electron density of acyl carbon atom, more will be the susceptibility of a nucleophile to attack it.
The Cl atom has strong - I effect and weakest +R effect because of the weak π-bond between the small sized C- atom and large sized Cl atom. Thus, in CH3COCl, acyl carbon has least electron density and hence, more susceptible for nucleophilic attack.
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