Alkyl isocyanides () exhibit fundamentally distinct chemical reactivity compared to alkyl cyanides (). If methyl isocyanide () undergoes complete chemical reduction utilizing , what is the exact ident

Question

Alkyl isocyanides ($R-NC$) exhibit fundamentally distinct chemical reactivity compared to alkyl cyanides ($R-CN$). If methyl isocyanide ($CH_3NC$) undergoes complete chemical reduction utilizing $LiAlH_4$, what is the exact identity of the resulting amine?

Prashant Kotian · Accepted Answer

Correct answer: D. Isocyanides feature the nitrogen atom structurally located between the alkyl chain and the terminal carbon. Complete powerful reduction utilizing specifically forces hydrogen onto both the carbon and the nitrogen atoms of the functional group, yielding entirely the secondary () amine, dimethylamine ().

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