The correct structure of the product A formed | vedclass

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(B) The reaction involves the catalytic hydrogenation of an $\alpha,\beta$-unsaturated ketone,specifically $cyclohex-2-en-1-one$,using $H_2$ gas in th

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Cyclohexanone

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(B) The reaction involves the catalytic hydrogenation of an $\alpha,\beta$-unsaturated ketone,specifically $cyclohex-2-en-1-one$,using $H_2$ gas in the presence of $Pd/C$ catalyst.Under mild conditions ($1$ atm pressure,room temperature),$Pd/C$ is a selective catalyst that can reduce the carbon-carbon double bond $(C=C)$ while leaving the carbonyl group $(C=O)$ intact.Therefore,the $C=C$ bond is hydrogenated to a $C-C$ single bond,converting $cyclohex-2-en-1-one$ into $cyclohexanone$.

The correct structure of the product $A$ formed in the reaction shown below is:
$Cyclohex-2-en-1-one \xrightarrow[{Pd/C, \text{ ethanol}}]{{H_2 \text{ (gas, 1 atm)}}} A$

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The correct structure of the product $A$ formed in the reaction shown below is:$Cyclohex-2-en-1-one \xrightarrow[{Pd/C, \text{ ethanol}}]{{H_2 \text{ (gas, 1 atm)}}} A$