6. Explain why one diastereomer is themodynamically more stable than the other. To do so, draw both chair conformations for cis-4-tert-butyleyclohexanol. Do the same for trans-4-tert- butyleyclohexanol. Label all 1,3-diazial interactions for these four species. Indicate the most stable chair conformation of cis-4-tert-butyleyclohexanol. Do the same for trans-4-tert-butyl- cyclohexanol. Which of these latter two species is the most stable?

6. Explain why one diastereomer is themodynamically more stable than the other. To do so, draw both chair conformations for cis-4-tert-butyleyclohexanol. Do the same for trans-4-tert- butyleyclohexanol. Label all 1,3-diazial interactions for these four species. Indicate the most stable chair conformation of cis-4-tert-butyleyclohexanol. Do the same for trans-4-tert-butyl- cyclohexanol. Which of these latter two species is the most stable?

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter14: Elimination

Section: Chapter Questions

Problem 46CTQ

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