Chapter 5: Q.13 (page 190)
Label each compound as R or S.
a.
b.
c.
d.
Short Answer
a. S isomer.
b. S isomer.
c. R isomer.
d. S isomer.
Chapter 5: Q.13 (page 190)
Label each compound as R or S.
a.
b.
c.
d.
a. S isomer.
b. S isomer.
c. R isomer.
d. S isomer.
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Get started for freea. Locate the stereogenic centres in the ball-and-stick model of lisinopril, a drug used to treat high blood pressure.
b. Label each stereogenic centre as R or S.
Draw all the possible stereoisomers for each compound and label pairs of enantiomers and diastereomers.
a.
b.
Draw a meso compound for each of the following molecules.
a.
b.
c.
The amino acid (S)-alanine has the physical characteristics listed under the structure.
a. What is the melting point of (R)-alanine?
b. How does the melting point of a racemic mixture of (R)- and (S)-alanine compare to the melting point of (S)-alanine?
c. What is the specific rotation of (R)-alanine, recorded under the same conditions as the reported rotation of (S)-alanine?
d. What is the optical rotation of a racemic mixture of (R)- and (S)-alanine?
e. Label each of the following as optically active or inactive: a solution of pure (S)-alanine; an equal mixture of (R)- and (S)-alanine; a solution that contains 75% (S)- and 25% (R)-alanine.
Locate the tetrahedral stereogenic center(s) in each compound. A molecule may have one or more stereogenic centers.
a.
b.
c.
d.
e.
f.
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