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Chemistry, 17.03.2020 19:56 125712

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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 itstable and present in a
concentration than the reacting conformation of the trans isomer.

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Explain why cis−1−chloro−2−methylcyclohexane undergoes E2 e...

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