Explanation
Alkyl and aryl cyanides (nitriles) can be reduced to their corresponding primary amines using lithium aluminium hydride ($$LiAlH_4$$) or catalytic hydrogenation.
Hence option A is correct.
Reduction of aryl nitriles in presence of $$LiAlH_4$$ Gives Aryl Amines. Alkyl and aryl cyanides (nitriles) can be reduce by $$LiAlH_4$$) or catalytic hydrogenation
Hence option B is correct.
The combined effect of the pushing effect of the alkyl group (+I effect), steric hindrance and the solvation of amines causes the basicity order to be:
$$NH_3< tertiary\ amine < primary \ amine< secondary\ amine$$.
$$HN(CH_3)_2$$ is secondary amine. So it is most basic.
Due to resonance there is a dispersal of positive charge on the benzene ring. This resonance accounts for the stability of the diazonium ion. Hence, diazonium salts of aromatic amines are more stable than those of aliphatic amines.
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