Fischer projections are primarily used to represent carbohydrates, which contain multiple stereocenters. The structure of carbohydrate D-glucose is shown below as a Fischer projection with each carbon numbered. For each carbon, find the absolute configuration (R or S) if it is a stereocenter, or indicate that it is not a stereocenter. Completely fill in the circle in front of your chosen answer. D-Glucose H- HO- H H CHO 2 3 4 5 -OH -H -OH -OH 6 CH₂OH Carbon 1: OR OS O Not a stereocenter Carbon 4: OR OS O Not a stereocenter Carbon 2: OR OS O Not a stereocenter Carbon 5: OR OS O Not a stereocenter Carbon 3: OR OS O Not a stereocenter Carbon 6: OR OS O Not a stereocenter
Fischer projections are primarily used to represent carbohydrates, which contain multiple stereocenters. The structure of carbohydrate D-glucose is shown below as a Fischer projection with each carbon numbered. For each carbon, find the absolute configuration (R or S) if it is a stereocenter, or indicate that it is not a stereocenter. Completely fill in the circle in front of your chosen answer. D-Glucose H- HO- H H CHO 2 3 4 5 -OH -H -OH -OH 6 CH₂OH Carbon 1: OR OS O Not a stereocenter Carbon 4: OR OS O Not a stereocenter Carbon 2: OR OS O Not a stereocenter Carbon 5: OR OS O Not a stereocenter Carbon 3: OR OS O Not a stereocenter Carbon 6: OR OS O Not a stereocenter
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
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![9. Fischer projections are primarily used to represent carbohydrates, which contain multiple
stereocenters. The structure of carbohydrate D-glucose is shown below as a Fischer projection with
each carbon numbered. For each carbon, find the absolute configuration (R or S) if it is a stereocenter,
or indicate that it is not a stereocenter. Completely fill in the circle in front of your chosen answer.
D-Glucose
H
HO
H
H
2
1
CHO
3
4
5
6
-OH
-H
OH
-OH
CH₂OH
Carbon 1:
OR
S
Not a stereocenter
Carbon 4:
OS
Not a stereocenter
Carbon 2:
OR
OS
O Not a stereocenter
Carbon 5:
OS
O Not a stereocenter
Carbon 3:
OR
OS
Not a stereocenter
Carbon 6:
OR
OS
O Not a stereocenter](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F0fcb0af8-b750-4635-b3ee-2f0c31e9ebdb%2F746ce0e4-290a-43aa-953f-f0a2260eeca6%2F5wys5l8_processed.jpeg&w=3840&q=75)
Transcribed Image Text:9. Fischer projections are primarily used to represent carbohydrates, which contain multiple
stereocenters. The structure of carbohydrate D-glucose is shown below as a Fischer projection with
each carbon numbered. For each carbon, find the absolute configuration (R or S) if it is a stereocenter,
or indicate that it is not a stereocenter. Completely fill in the circle in front of your chosen answer.
D-Glucose
H
HO
H
H
2
1
CHO
3
4
5
6
-OH
-H
OH
-OH
CH₂OH
Carbon 1:
OR
S
Not a stereocenter
Carbon 4:
OS
Not a stereocenter
Carbon 2:
OR
OS
O Not a stereocenter
Carbon 5:
OS
O Not a stereocenter
Carbon 3:
OR
OS
Not a stereocenter
Carbon 6:
OR
OS
O Not a stereocenter
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