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(D) $1$. The first step is the oxidation of cyclohexanol using $CrO_3$ to form cyclohexanone.$2$. The second step is the reaction of cyclohexanone wit

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$N$-methylcyclohexanamine

Vedclass · Answer

(D) $1$. The first step is the oxidation of cyclohexanol using $CrO_3$ to form cyclohexanone.$2$. The second step is the reaction of cyclohexanone with methylamine $(CH_3NH_2)$,which is a nucleophilic addition-elimination reaction forming an imine ($N$-methylcyclohexanimine).$3$. The third step is the catalytic hydrogenation of the imine using $H_2/Pd$,which reduces the $C=N$ double bond to a $C-NH$ single bond,resulting in the final product $[X]$,which is $N$-methylcyclohexanamine.

The product $[X]$ of the given reaction is:

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