Stereochemistry Problem Set
Name ______________________________
1. Label the following as chiral or achiral.
CH
3
CH
3
H3
C
CH
3
Br
I
CH
3
CH
3
CH
3
CH
3
2. Circle or supply the correct answer.
a. Which of the following is expected to rotate the plane of polarized light?
b. The (-)-isomer of any compound MUST be levorotatory?
c. Which of the following tells you NOTHING (in the absence of additional information) about
the molecule's absolute configuration?
d. Cis-trans
isomers are correctly described as--
e. For a molecule containing five chiral (stereogenic) centers, the maximum number of
stereoisomers is--
3. Give the stereochemical relationship between Compound A below and the five compounds B-F by
writing "enantiomer," "diastereomer," "identical," or "structural isomer" in the appropriate blanks.
IGNORE DIFFERENCES IN CONFORMATION.
4. Using the Fischer Projections below for the question below.
CH2
CH3
CH2
CH3
CH2
CH3
CH2
CH3
Using the letters below the frameworks to designate the structures that fit the following definitions. If no
example exists, write "none" in the blank. NOTE: Points will be deducted for extra
answers, even if
correct.
a. one
pair of enantiomers __________
b. one
pair of diastereomers __________
c. one
meso compound __________
d. one
compound with the R configuration at carbon 2 (the lower "rung" on the framework) __________
e. one
compound that, by itself, is optically inactive __________