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(B) The reaction sequence is as follows:$1$. Benzene reacts with cyclohexene in the presence of $H_2SO_4$ (acid-catalyzed alkylation) to form cyclohex

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(B) The reaction sequence is as follows:$1$. Benzene reacts with cyclohexene in the presence of $H_2SO_4$ (acid-catalyzed alkylation) to form cyclohexylbenzene.$2$. Treatment with $NBS$ ($N$-bromosuccinimide) followed by $alc. KOH$ introduces a double bond,forming $1$-phenylcyclohex-$1$-ene (compound $(B)$).$3$. Epoxidation of $1$-phenylcyclohex-$1$-ene using a peroxyacid $(RCO_3H)$ yields $1$-phenyl-$-oxabicyclo[4.1.0]heptane$ (compound $(C)$).The correct structure for $(C)$ is the epoxide of $1$-phenylcyclohex-$1$-ene.

Product $(C)$ is

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