In the given set of reactions,the IUPAC name | vedclass

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(D) $AgCN$ is a covalent compound,therefore,the nucleophilic attack occurs through the nitrogen atom of the $CN^-$ group,leading to the formation of a

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$N-	ext{Methylpropan-2-amine}$

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(D) $AgCN$ is a covalent compound,therefore,the nucleophilic attack occurs through the nitrogen atom of the $CN^-$ group,leading to the formation of an isocyanide $(R-NC)$.Step $1$: $CH_3-CH(Br)-CH_3 + AgCN \xrightarrow{\Delta} CH_3-CH(NC)-CH_3$ (Product $X$ is isopropyl isocyanide).Step $2$: Reduction of isocyanide with $LiAlH_4$ yields a secondary amine.$CH_3-CH(NC)-CH_3 \xrightarrow{LiAlH_4} CH_3-CH(NHCH_3)-CH_3$ (Product $Y$ is $N-	ext{methylpropan-2-amine}$).

In the given set of reactions,the $IUPAC$ name of product '$Y$' is:
$2-\text{Bromopropane}$ $\xrightarrow[\text{alc. / heat}]{AgCN} X$ $\xrightarrow{LiAlH_4} Y$

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In the given set of reactions,the $IUPAC$ name of product '$Y$' is: $2-\text{Bromopropane}$ $\xrightarrow[\text{alc. / heat}]{AgCN} X$ $\xrightarrow{LiAlH_4} Y$