10. Identify the higher energy and lower energy forms of two substituted cyclohexanes, for example t-butyl cyclohexane. Which form (t-butyl axial or equatorial) has a higher energy, and why? more stable by 24 kJ/mol H3C.,CH3 CH3 Key >1 CCH3 CH3 H. tert-butyl group axial tert-butyl group equatorial

Organic Chemistry
9th Edition
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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explain and answer the "why" please. also, what makes one axial and the other equatorial? and what does Keq have to do with it ?

10. Identify the higher energy and lower energy forms of two substituted cyclohexanes, for example
t-butyl cyclohexane. Which form (t-butyl axial or equatorial) has a higher energy, and why?
more stable by 24 kJ/mol
H3C.,CH3
CH3
Key >1
CCH3
CH3
H.
tert-butyl group axial
tert-butyl group equatorial
Transcribed Image Text:10. Identify the higher energy and lower energy forms of two substituted cyclohexanes, for example t-butyl cyclohexane. Which form (t-butyl axial or equatorial) has a higher energy, and why? more stable by 24 kJ/mol H3C.,CH3 CH3 Key >1 CCH3 CH3 H. tert-butyl group axial tert-butyl group equatorial
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