Which is more stable, cis–1,4–dimethylcyclohexane or the trans isomer? Draw the structure of the morestable isomer. Your structure should clearly distinguish between all axial and equatorial positions.Draw the most stable conformer of trans-1-t-butyl–3–methylcyclohexane. Your structure shouldclearly distinguish between all axial and equatorial positions. Given that pKa for phenol is 9.95 and pKa for the ammonium ion is 9.24, will the following reaction befavorable? (Will the products be favored at equilibrium?)HO+ NH3phenoxide ionphenolpKa = 9.95ammoniaammonium ionpKa = 9.24

As per the rules only the first question can be answered.

Answered: Which is more stable,…

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

Chapter21: Benzene And The Concept Of Aromaticity

Section: Chapter Questions

Problem 21.33P

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Which is more stable, cis–1,4-dimethylcyclohexane or the trans isomer? Draw the structure of the more stable isomer. Your structure should clearly distinguish between all axial and equatorial positions.