Chemistry: 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.

Explain why cis−1−chloro−2−methylcyclohexane undergoes

Ответ:

meth77

10.01.2022

Chemistry

Both chloro and methyl groups axial
More stable
Higher concentration

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Ответ:

shadowangel84

04.01.2021

Chemistry

maybe option 3 idk

Explanation:

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

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