For the Newman projection shown below, the back carbon is being rotated clockwise as illustrated below (B through G are left blank for you to predict what they will look like). Select the conformation(s) with the highest energy/energies. Select all that apply. 0: 0° 60° 120° 180° 240° 300° 360° D E A.A B. B C.C D. D E. E F. F G.G CI H H H A OH B F

For the Newman projection shown below, the back carbon is being rotated clockwise as illustrated below (B through G are left blank for you to predict what they will look like). Select the conformation(s) with the highest energy/energies. Select all that apply. 0: 0° 60° 120° 180° 240° 300° 360° D E A.A B. B C.C D. D E. E F. F G.G CI H H H A OH B F

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter7: Cycloalkanes

Section: Chapter Questions

Problem 14CTQ

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Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This group is called an ethyl group and can be considered a sphere about twice the sizeof a methyl group. Draw the following Newman projections sighting down the C1C2 bond... a. The lowest potential energy conformation. b. The highest potential energy staggered conformation.
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