1. Between trans-3-isopropylcyclohexanamine and cis-3-isopropylcyclohexanamine, which stereoisomer and configuration is the most stable? Why? Show your depicted physical model of these molecules and point out where steric strain occurs.

1. Between trans-3-isopropylcyclohexanamine and cis-3-isopropylcyclohexanamine, which stereoisomer and configuration is the most stable? Why? Show your depicted physical model of these molecules and point out where steric strain occurs.

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

Chapter10: Alcohols

Section: Chapter Questions

Problem 10.33P: Two diastereomeric sets of enantiomers, A/B and C/D, exist for 3-bromo-2-butanol. When enantiomer A...

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Question

Between trans-3-isopropylcyclohexanamine and cis-3-isopropylcyclohexanamine, which stereoisomer
and configuration is the most stable? Why? Show your depicted physical model of these molecules and
point out where steric strain occurs.
1.
cis

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