Explain why cis−1−chloro−2−methylcyclohexane undergoes e2 elimination much faster than its trans isomer.
the reacting conformation of the cis isomer has
group(s) axial, making it stable and present in a
concentration than the reacting conformation of the trans isomer.
Answers: 3
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Explain why cis−1−chloro−2−methylcyclohexane undergoes e2 elimination much faster than its trans iso...
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