The major product formed in the following rea | vedclass

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(C) $PCC$ (Pyridinium chlorochromate) is a selective oxidizing agent that oxidizes primary alcohols to aldehydes and secondary alcohols to ketones. In

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(C) $PCC$ (Pyridinium chlorochromate) is a selective oxidizing agent that oxidizes primary alcohols to aldehydes and secondary alcohols to ketones. In the given reactant,there is a primary allylic alcohol group $(-CH_2OH)$ and a secondary alcohol group $(-OH)$ attached to the ring. $PCC$ will oxidize the primary alcohol to an aldehyde and the secondary alcohol to a ketone. The $-OCOCH_3$ group remains unaffected under these conditions. Therefore,the product is the one where the primary alcohol is converted to an aldehyde and the secondary alcohol is converted to a ketone.

List-$I$	List-$II$
$A$. Grignard reagent	$1$. $H_2 / Pd-BaSO_4$
$B$. Clemmensen reduction	$2$. $N_2H_4 / KOH / (CH_2OH)_2$
$C$. Rosenmund reduction	$3$. $CH_3MgX$
$D$. Wolff-Kishner reduction	$4$. $Zn-Hg / \text{conc. } HCl$
	$5$. $H_2 / Ni$

The major product formed in the following reaction is
(Structure of the reactant) $\xrightarrow[{CHCl_3}]{{PCC}}$

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List-$I$ List-$II$
$A$. Grignard reagent $1$. $H_2 / Pd-BaSO_4$
$B$. Clemmensen reduction $2$. $N_2H_4 / KOH / (CH_2OH)_2$
$C$. Rosenmund reduction $3$. $CH_3MgX$
$D$. Wolff-Kishner reduction $4$. $Zn-Hg / \text{conc. } HCl$
$5$. $H_2 / Ni$

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The major product formed in the following reaction is(Structure of the reactant) $\xrightarrow[{CHCl_3}]{{PCC}}$