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Question

(A) The reaction proceeds in two steps:$1$. Cyclohexane reacts with $Br_2$ in the presence of $h
u$ (ultraviolet light) to undergo free radical subst

Vedclass · Accepted Answer

Bicyclohexyl

Vedclass · Answer

(A) The reaction proceeds in two steps:$1$. Cyclohexane reacts with $Br_2$ in the presence of $h
u$ (ultraviolet light) to undergo free radical substitution,forming bromocyclohexane as product $A$.$2$. Bromocyclohexane reacts with $Na$ in the presence of dry ether,which is a Wurtz reaction. Two molecules of bromocyclohexane couple to form bicyclohexyl as product $B$.

Product $B$ is

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