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

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter3: Organic Compounds: Alkanes And Their Stereochemistry

Section3.SE: Something Extra

Problem 47AP: Draw the most stable conformation of 1,4-dichlorobutane, using wedges and dashes to represent bonds...

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Draw the most stable conformation of 1,4-dichlorobutane, using wedges and dashes to represent bonds coming out of the paper and going behind the paper, respectively.
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