The product of the reaction given below is :

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(D) The reaction proceeds in two steps: $1$. Allylic bromination using $NBS$ ($N$-Bromosuccinimide) under $hv$ (light) conditions,which introduces a b

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$4-$tert-butylcyclohex$-2-$en$-1-$ol.

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(D) The reaction proceeds in two steps: $1$. Allylic bromination using $NBS$ ($N$-Bromosuccinimide) under $hv$ (light) conditions,which introduces a bromine atom at the allylic position. $2$. Nucleophilic substitution of the bromine atom with a hydroxyl group using $H_2O/K_2CO_3$,resulting in the formation of an allylic alcohol. The final product is $4$-tert-butylcyclohex-$2$-en-$1$-ol.

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