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
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ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter3: Organic Compounds: Alkanes And Their Stereochemistry
Section3.SE: Something Extra
Problem 52AP: Increased substitution around a bond leads to increased strain. Take the four substituted butanes...
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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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