< (S)-carvone is an optically active compound with a specific rotation of +61.1°. A solution of carvone stereoisomers has an observed specific rotation of 25.0°. 1 4 Calculate the percent enantiomeric excess (%ee) of this mixture. 7 +/- 2 Question 1 of 2 5 8 %ee 3 6 9 0 Submit Tap here or pull up for additional resources C X C x 100
< (S)-carvone is an optically active compound with a specific rotation of +61.1°. A solution of carvone stereoisomers has an observed specific rotation of 25.0°. 1 4 Calculate the percent enantiomeric excess (%ee) of this mixture. 7 +/- 2 Question 1 of 2 5 8 %ee 3 6 9 0 Submit Tap here or pull up for additional resources C X C x 100
Chapter92: Polarimetry
Section: Chapter Questions
Problem 2P
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![(S)-carvone is an optically
active compound with a
specific rotation of +61.1°.
A solution of carvone
stereoisomers has an observed
specific rotation of 25.0°.
1
Calculate the percent
enantiomeric excess (%ee) of
this mixture.
4
7
+/-
2
Question 1 of 2
5
8
%ee
3
6
9
0
Submit
Tap here or pull up for additional resources
|||
Г
Xx
C
x 100](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ff35f8f89-65fc-4b90-98e9-68f8eaa1b3da%2F4a3dd4c0-08fe-4d43-a827-b45bb66e2564%2F3gi5nao_processed.jpeg&w=3840&q=75)
Transcribed Image Text:(S)-carvone is an optically
active compound with a
specific rotation of +61.1°.
A solution of carvone
stereoisomers has an observed
specific rotation of 25.0°.
1
Calculate the percent
enantiomeric excess (%ee) of
this mixture.
4
7
+/-
2
Question 1 of 2
5
8
%ee
3
6
9
0
Submit
Tap here or pull up for additional resources
|||
Г
Xx
C
x 100
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