2. Draw structures showing stereochemistry as requested. (Except at the stereocenter draw the structure condensed). (a) (2S,3S)-2-bromo-3-chlorobutane (Except for the Fischer projection draw the conformation as staggered.) perspective drawing sawhorse drawing Newman projection Fischer projection (longest C chain horizontal) (longest C chain horizontal) (longest C chain vertical) (longest C chain vertical) (b) (1R,2S)-1-bromo-2-methylcyclopentane (Do you see that this is an enantiomer of the cis diastereomer?) ring perpendicular to plane of paper ring in plane of paper (perspective)
2. Draw structures showing stereochemistry as requested. (Except at the stereocenter draw the structure condensed). (a) (2S,3S)-2-bromo-3-chlorobutane (Except for the Fischer projection draw the conformation as staggered.) perspective drawing sawhorse drawing Newman projection Fischer projection (longest C chain horizontal) (longest C chain horizontal) (longest C chain vertical) (longest C chain vertical) (b) (1R,2S)-1-bromo-2-methylcyclopentane (Do you see that this is an enantiomer of the cis diastereomer?) ring perpendicular to plane of paper ring in plane of paper (perspective)
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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2

Transcribed Image Text:2.
Draw structures showing stereochemistry as requested. (Except at the stereocenter draw the structure
condensed).
(a) (2S,3S)-2-bromo-3-chlorobutane (Except for the Fischer projection draw the conformation as staggered.)
perspective drawing
sawhorse drawing
Newman projection
Fischer projection
(longest C chain horizontal)
(longest C chain horizontal)
(longest C chain vertical)
(longest C chain vertical)
(b) (1R,2S)-1-bromo-2-methylcyclopentane (Do you see that this is an enantiomer of the cis diastereomer?)
ring perpendicular to plane of paper
ring in plane of paper (perspective)
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