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 C CH3 CH3 HaC-C Ke >1 H. H tert-butyl group axial tert-butyl group equatorial

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 C CH3 CH3 HaC-C Ke >1 H. 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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