Give a plausible explanation for the following. There are two NH2 groups in semicarbazide. However, only one such group is involved in the formation of semicarbazones.
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Solution
Semicarbazide undergoes resonance as given on the structure.
One of the anion group involves in resonance and hence the electron density on this −NH2 group decreases and it does not act as a nucleophile. But the other group (attached to −NH) has a lone pair of electrons which are not involved in resonance and is available for the nucleophilic attack on carbonyl group tp product semicarbazones.