Trans-1,2-dimethylcyclohexane is more stable than cis-1,2-dimethylcyclohexane because? (A) The trans isomer has one axial and one equatorial methyl group. (B) The trans isomer has two equatorial groups. (C) The trans isomer has the two CH3 groups further away from each other. (D) The trans isomer has two CH3 groups in an anti-arrangement.

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter2: Alkanes And Cycloalkanes
Section2.6: Cis,trans Isomerism In Cycloalkanes And Bicycloalkanes
Problem 2.13P: Following is a planar hexagon representation for one isomer of 1,2,4-trimethylcyclohexane. Draw the...
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Trans-1,2-dimethylcyclohexane is more stable than cis-1,2-dimethylcyclohexane because?
(A) The trans isomer has one axial and one equatorial methyl group.
(B) The trans isomer has two equatorial groups.
(C) The trans isomer has the two CH3 groups further away from each other.
(D) The trans isomer has two CH3 groups in an anti-arrangement.
Transcribed Image Text:Trans-1,2-dimethylcyclohexane is more stable than cis-1,2-dimethylcyclohexane because? (A) The trans isomer has one axial and one equatorial methyl group. (B) The trans isomer has two equatorial groups. (C) The trans isomer has the two CH3 groups further away from each other. (D) The trans isomer has two CH3 groups in an anti-arrangement.
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