Identify the product (C) in the following ser | vedclass

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(B) $1$. The reaction starts with cyclopentane. Treatment with $Br_2$ in the presence of $hv$ (free radical substitution) gives bromocyclopentane as p

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$3-$Bromocyclopent$-1-$ene

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(B) $1$. The reaction starts with cyclopentane. Treatment with $Br_2$ in the presence of $hv$ (free radical substitution) gives bromocyclopentane as product $(A)$.$2$. Bromocyclopentane $(A)$ reacts with alcoholic $KOH$ (dehydrohalogenation) to form cyclopentene as product $(B)$.$3$. Cyclopentene $(B)$ reacts with $NBS$ ($N$-Bromosuccinimide),which is a specific reagent for allylic bromination,to form $3-$bromocyclopent$-1-$ene as product $(C)$.

Identify the product $(C)$ in the following series of reaction:
$\text{Cyclopentane}$ $\xrightarrow{Br_2, hv} A$ $\xrightarrow{\text{alc. KOH}} B$ $\xrightarrow{\text{NBS}} C$

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Identify the product $(C)$ in the following series of reaction:$\text{Cyclopentane}$ $\xrightarrow{Br_2, hv} A$ $\xrightarrow{\text{alc. KOH}} B$ $\xrightarrow{\text{NBS}} C$