Which of the following compounds gives diaste | vedclass

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(A) The addition of $Br_2$ to an alkene is an anti-addition reaction. When an alkene already contains a chiral center,the addition of $Br_2$ creates n

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$3-Methylcyclopentene$

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(A) The addition of $Br_2$ to an alkene is an anti-addition reaction. When an alkene already contains a chiral center,the addition of $Br_2$ creates new chiral centers. The resulting products will be diastereomers because the configuration at the existing chiral center remains unchanged,while the new chiral centers are formed in different relative configurations. $3-Methylcyclopentene$ contains a chiral center at the $C-3$ position. Upon reaction with $Br_2$ in $CCl_4$,the anti-addition of bromine across the double bond results in the formation of two diastereomeric products,as the existing chiral center at $C-3$ is not involved in the reaction.

Which of the following compounds gives diastereomers when treated with $Br_2$ in $CCl_4$?

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