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Given cyclohexane in a chair conformation, substitute two of the H labels with bromine and chlorine to construct the more stable conformation of cis-1-bromo-3-chlorocyclohexane. Use the numbering provided on the ring.

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Answer:

the answer is 1-Bromo-3-chlorobenzene. Attached file is the answer.

Explanation:

Equatorial position of bonds provides greater stability for the chair conformation.

Cis-configuration is ensured by aligning both dash bonds to be downwards directed.

The final product is a compound 1-Bromo-3-chlorobenzene.

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