Draw structures showing stereochemistry as requested. (Except at the stereocenter draw the structure condensed). 2. (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) (25,3)- 2-bromo-3-ch CH - CHS -Bh CI. 4 CHS H- ci me CH3 CHS CHS (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) Br Ochz - (R,2s) -1-bromo--

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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)
CH
(25,35)- 2-bromo-3-ch
-Bh
Sc me
CH3
CHs
(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)
O 48-
(R, 2s) - 1-bromo--
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) CH (25,35)- 2-bromo-3-ch -Bh Sc me CH3 CHs (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) O 48- (R, 2s) - 1-bromo--
Expert Solution
Step 1

R/S nomenclature is based on CIP rule which states that higher is the atomic number of directly attached atom, higher will be the priority. 

When 4th group is vertical : 1 to 2 to 3 clockwise rotation R and anti-clockwise rotation S.

When 4th group is horizontal : 1 to 2 to 3 clockwise rotation S and anti-clockwise rotation R.

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