8. Explain why (1S,3R)-3-tert-butylcyclohexyl bromide undergoes E2 elimination with potassium tert-butoxide very slowly while the (1R,3R) reacts much more rapidly.

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8. Explain why (1S,3R)-3-tert-butylcyclohexyl bromide undergoes E2 elimination with
potassium tert-butoxide very slowly while the (1R,3R) reacts much more rapidly.
Transcribed Image Text:8. Explain why (1S,3R)-3-tert-butylcyclohexyl bromide undergoes E2 elimination with potassium tert-butoxide very slowly while the (1R,3R) reacts much more rapidly.
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