In his classic studies of stereochemistry and optical activity in organic compounds, Pasteur measured the optical activity of many solutions. For the naturally occurring enantiomer of tartaric acid, [a],20 = +12.4°. What is the % of the (+)-enantiomer in the mixture if the observed rotation is a = -6.0°, with a concentration of 0.54 g/mL in a 2.00 dm polarimeter tube? A. 25.8% B. 27.6% C. 44.8% D. 72.4% E. 74.2% A O B D O E

Basic Clinical Laboratory Techniques 6E
6th Edition
ISBN:9781133893943
Author:ESTRIDGE
Publisher:ESTRIDGE
Chapter6: Basic Clinical Chemistry
Section6.1: Introduction To Clinical Chemistry
Problem 12RQ
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In his classic studies of stereochemistry and optical activity in organic compounds,
Pasteur measured the optical activity of many solutions. For the naturally occurring
enantiomer of tartaric acid, [a]p20 = +12.4°. What is the % of the (+)-enantiomer in the
mixture if the observed rotation is a = -6.0°, with a concentration of 0.54 g/mL in a
2.00 dm polarimeter tube?
A. 25.8%
В. 27.6%
C. 44.8%
D. 72.4%
E. 74.2%
А
C
O E
B.
Transcribed Image Text:In his classic studies of stereochemistry and optical activity in organic compounds, Pasteur measured the optical activity of many solutions. For the naturally occurring enantiomer of tartaric acid, [a]p20 = +12.4°. What is the % of the (+)-enantiomer in the mixture if the observed rotation is a = -6.0°, with a concentration of 0.54 g/mL in a 2.00 dm polarimeter tube? A. 25.8% В. 27.6% C. 44.8% D. 72.4% E. 74.2% А C O E B.
What is the relationship between the following pair.
CH,Br
CI
CH3
CI
CH2CH3
Но
HOl..
CH,Br
CH2CH3
CH3
Enantiomers
Diastereomers
Conformers
O Identical
O Constitutional isomers
Transcribed Image Text:What is the relationship between the following pair. CH,Br CI CH3 CI CH2CH3 Но HOl.. CH,Br CH2CH3 CH3 Enantiomers Diastereomers Conformers O Identical O Constitutional isomers
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