A solution of cyclohexene in benzene is stirr | vedclass

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Question

(A) The reaction involves the protonation of cyclohexene by concentrated $H_2SO_4$ to form a cyclohexyl carbocation.This carbocation then undergoes an

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cyclohexylbenzene

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(A) The reaction involves the protonation of cyclohexene by concentrated $H_2SO_4$ to form a cyclohexyl carbocation.This carbocation then undergoes an electrophilic aromatic substitution $(S_EAr)$ reaction with benzene.The cyclohexyl carbocation acts as an electrophile and attacks the benzene ring to form cyclohexylbenzene.The reaction sequence is: Cyclohexene $+ H^+ ightarrow$ Cyclohexyl carbocation $\xrightarrow{	ext{Benzene}} 	ext{Cyclohexylbenzene}$.

$A$ solution of cyclohexene in benzene is stirred at $0 \ ^oC$ while concentrated sulphuric acid is added. After washing away the acid and removing the excess benzene,what product is isolated?

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