Write the structure for the most stable conformer of trans-1-iodo-3-ethylcyclohexane. Calculate the percentages of both conformers at 25 °C from the data below. R=1.99 cal/mol K Free Energy difference between equatorial and axial substituents: Substituent AG I 0.4 kcal/mol CH5 2.1 kcal/mol

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
Section: Chapter Questions
Problem 2.45P: Gibbs free energy differences between axial-substituted and equatorial-substituted chair...
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Write the structure for the most stable conformer of trans-1-iodo-3-ethylcyclohexane.
Calculate the percentages of both conformers at 25 °C from the data below.
R=1.99 cal/mol K
5.
Free Energy difference between equatorial and axial substituents:
Substituent
AG
0.4 kcal/mol
I
CHs
2.1 kcal/mol
Transcribed Image Text:Write the structure for the most stable conformer of trans-1-iodo-3-ethylcyclohexane. Calculate the percentages of both conformers at 25 °C from the data below. R=1.99 cal/mol K 5. Free Energy difference between equatorial and axial substituents: Substituent AG 0.4 kcal/mol I CHs 2.1 kcal/mol
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