Identify the final product C in the following | vedclass

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(A) $1$. The first step is an intramolecular Wurtz reaction: $Br-(CH_2)_5-Br \xrightarrow{Na, 	ext{D.E.}} 	ext{cyclopentane} (A)$.$2$. The second st

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(A) $1$. The first step is an intramolecular Wurtz reaction: $Br-(CH_2)_5-Br \xrightarrow{Na, 	ext{D.E.}} 	ext{cyclopentane} (A)$.$2$. The second step is free radical bromination: $	ext{cyclopentane} \xrightarrow{Br_2, \Delta} 	ext{bromocyclopentane} (B)$.$3$. The third step is dehydrohalogenation using alcoholic $KOH$: $	ext{bromocyclopentane} \xrightarrow{	ext{alc. KOH}, \Delta} 	ext{cyclopentene} (C)$.

Identify the final product $C$ in the following reaction sequence:
$Br-(CH_2)_5-Br$ $\xrightarrow{Na, \text{D.E.}} A$ $\xrightarrow{Br_2, \Delta} B$ $\xrightarrow{\text{alc. KOH}, \Delta} C$

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Identify the final product $C$ in the following reaction sequence:$Br-(CH_2)_5-Br$ $\xrightarrow{Na, \text{D.E.}} A$ $\xrightarrow{Br_2, \Delta} B$ $\xrightarrow{\text{alc. KOH}, \Delta} C$