for-the-elimination-reaction-of-the-cis-1-iodo-4-isopropylcyclohexane-and-trans-

Question

The elimination reactions of the cis-1-iodo-4-isopropylcyclohexane and trans-1-iodo-4-isopropylcyclohexane with sodium methoxide in methanol form 4-isopropylcyclohex-1-ene. Explain the reason why the cis-1-iodo-4-isopropylcyclohexane is more reactive than the trans-1-iodo-4-isopropylcyclohexane.

Accepted Answer

The isopropyl substituent is in a more stable equatorial position.

Answer

The isopropyl substituent is in a more stable axial position.

Answer

The isopropyl substituent is located three carbons away.

Answer

The isopropyl substituent is in a less stable equatorial position.

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The elimination reactions of the cis-1-iodo-4-isopropylcyclohexane and trans-1-iodo-4-isopropylcyclohexane with sodium methoxide in methanol form 4-isopropylcyclohex-1-ene. Explain the reason why the cis-1-iodo-4-isopropylcyclohexane is more reactive than the trans-1-iodo-4-isopropylcyclohexane.