Identify C in the following sequence of react | vedclass

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(B) The reaction sequence is as follows:$1$. $2	ext{-methylcyclohexanecarboxylic acid}$ reacts with $SOCl_2$ to form the acid chloride,$A$ $(2	ext{-

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$2-$methylcyclohexanecarbonitrile

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(B) The reaction sequence is as follows:$1$. $2	ext{-methylcyclohexanecarboxylic acid}$ reacts with $SOCl_2$ to form the acid chloride,$A$ $(2	ext{-methylcyclohexanecarbonyl chloride})$.$2$. The acid chloride $A$ reacts with $NH_3$ to form the amide,$B$ $(2	ext{-methylcyclohexanecarboxamide})$.$3$. The amide $B$ undergoes dehydration with $P_4O_{10}$ upon heating to form the nitrile,$C$ $(2	ext{-methylcyclohexanecarbonitrile})$.The stereochemistry is retained throughout the reaction sequence. The starting material has the $-COOH$ group and $-CH_3$ group in a specific relative configuration (trans). Therefore,the final product $C$ will also have the $-CN$ group and $-CH_3$ group in the same relative configuration.

Identify $C$ in the following sequence of reactions:
$2\text{-methylcyclohexanecarboxylic acid}$ $\xrightarrow{SOCl_2} A$ $\xrightarrow{NH_3} B$ $\xrightarrow{P_4O_{10}, \text{heat}} C(C_8H_{13}N)$

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Identify $C$ in the following sequence of reactions:$2\text{-methylcyclohexanecarboxylic acid}$ $\xrightarrow{SOCl_2} A$ $\xrightarrow{NH_3} B$ $\xrightarrow{P_4O_{10}, \text{heat}} C(C_8H_{13}N)$