The major products A and B for the following | vedclass

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(B) $1$. In the first step,the reaction of $2-(2-iodoethyl)cyclohexanone$ with $KCN$ in $DMSO$ proceeds via an $S_N2$ mechanism. The $CN^-$ nucleophil

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Product $A$ is a substituted cyclohexanone with a cyano group and $B$ is a substituted cyclohexanol with an amine group.

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(B) $1$. In the first step,the reaction of $2-(2-iodoethyl)cyclohexanone$ with $KCN$ in $DMSO$ proceeds via an $S_N2$ mechanism. The $CN^-$ nucleophile replaces the iodide ion,resulting in $2-(2-cyanoethyl)cyclohexanone$ as product $A$.$2$. In the second step,the catalytic hydrogenation of product $A$ using $H_2/Pd$ reduces both the ketone group to a secondary alcohol and the nitrile group to a primary amine. Thus,product $B$ is $2-(3-aminopropyl)cyclohexanol$.

List-$I$ Reaction	List-$II$ Reagents
$A$. Hoffmann Degradation	$I$. Conc. $KOH, \Delta$
$B$. Clemmensen reduction	$II$. $CHCl_3, NaOH / H_3O^{+}$
$C$. Cannizzaro reaction	$III$. $Br_2, NaOH$
$D$. Reimer-Tiemann reaction	$IV$. $Zn-Hg / HCl$

The major products $A$ and $B$ for the following reactions are,respectively:

Similar Questions

Match List-$I$ with List-$II$.

List-$I$ Reaction List-$II$ Reagents

$A$. Hoffmann Degradation $I$. Conc. $KOH, \Delta$

$B$. Clemmensen reduction $II$. $CHCl_3, NaOH / H_3O^{+}$

$C$. Cannizzaro reaction $III$. $Br_2, NaOH$

$D$. Reimer-Tiemann reaction $IV$. $Zn-Hg / HCl$

The product of the following reaction is :

The above reduction can be best carried out by

The final product $(C)$ in the given reaction sequence is
$C_6H_5COOH$ $\xrightarrow{SOCl_2} (A)$ $\xrightarrow[\text{anhy. } AlCl_3]{C_6H_6} (B)$ $\xrightarrow[\text{(ii) } KOH / (CH_2OH)_2]{\text{(i) } NH_2-NH_2} (C)$

Which of the following is a solid trimer of formaldehyde?

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