Please write the following mechanism with all of the intermediates, using a carboxylic acid derivative transformation:
Benzoyl chloride + LDA ---> N,N-diisopropyl benzamide
Thank you
LDA is primarily a base used to extract the acidic enol H from aldehyde/ ketones.
But benzoyl chloride doesn't have any such enolisable H. Hence, here, LDA behaves as a nucleophile and attacks the C of C=O group.
The carboxylic acid derivative transformation occuring is : acid chloride to amide
Please write the following mechanism with all of the intermediates, using a carboxylic acid derivative transformation:...
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