Question

Quinoline undergoes nucleophilic substitution on heating with NaNH2 to give

Answer 1

Answer:

2-amino pyridine

Explanation:

Here, sodium amide is used as the nucleophile yielding 2-aminopyridine. The hydride ion released in this reaction combines with a proton of an available amino group, forming a hydrogen molecule.

if it reacts under excess of NaNH2 then it will give rise to 2,6-diaminopyridine

Sodium amide in excess is used as the nucleophile yielding 2,6-diaminopyridine. The hydride ion released in this reaction combines with a proton of an available amino group, forming a hydrogen molecule

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