4. Draw the structures of the two enantiomers of 2,3-dibromo-3-phenylpropanoic acid that were produced by the reaction. Assign the absolute configuration (R or S) at the chiral centers in each of the product structures.

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Use the data table to answer the question.

4. Draw the structures of the two enantiomers of 2,3-dibromo-3-phenylpropanoic acid that
were produced by the reaction. Assign the absolute configuration (R or S) at the chiral
centers in each of the product structures.
Transcribed Image Text:4. Draw the structures of the two enantiomers of 2,3-dibromo-3-phenylpropanoic acid that were produced by the reaction. Assign the absolute configuration (R or S) at the chiral centers in each of the product structures.
Molecular
Weight
Milligrams
Millimoles
Concentration
Volume
Trans-cinnamic acid
148.1586 g/mol
159.808
(149x1000) = 149mg •128 x1000 =
149.
128
1.006
=
148. 1586 mmol 159.808
n/a
Bromine in acetic acid
g/mal
n/a
Equivalents 1.006.801.125
•801
Imey 2
1
= .801
128mg bodonge our /02.55 mg
an
DC.
1 M
mmol
om 10 dan M
2,3-dibromo-hydrocinnamic acid
= .801 mL
307.97 g/mol
333 x 307.97=
801.4156)=333
•333
.801
n/a
pla
=.42
Transcribed Image Text:Molecular Weight Milligrams Millimoles Concentration Volume Trans-cinnamic acid 148.1586 g/mol 159.808 (149x1000) = 149mg •128 x1000 = 149. 128 1.006 = 148. 1586 mmol 159.808 n/a Bromine in acetic acid g/mal n/a Equivalents 1.006.801.125 •801 Imey 2 1 = .801 128mg bodonge our /02.55 mg an DC. 1 M mmol om 10 dan M 2,3-dibromo-hydrocinnamic acid = .801 mL 307.97 g/mol 333 x 307.97= 801.4156)=333 •333 .801 n/a pla =.42
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