6. Shown below is the Fisher projection of (R)-2-bromo-(S)-3-chlorobutane. Draw the mirror image of this stereoisomer and assign the RIS configurations of each chiral carbons for both isomers. H. CH3 Br CH3 CI H. mirror plane

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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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are
other unmodified S molecule from 4. Are they enantiomers or are they
model with the
identical?
Draw the mirror image of this stereoisomer and assign the R/S configurations of
each chiral carbons for both isomers.
6.
Shown below is the Fisher projection of (R)-2-bromo-(S)-3-chlorobutane.
CH3
-Br
CH3 CI
H.
mirror plane
7.
Make models of both stereoisomers in question 6. Test the models for
superimposability. Secure the initials of your TA after showing them your
physical model of (R)-2-bromo-(S)-3-chlorobutane.
initials
In the space below draw Fisher projections of the two stereoisomers of 2-
thich are diastereomers of the stereoisomers shown in
nnstructed for question 7 and switch two
del represented by one of the
mmetric centers.
Transcribed Image Text:are other unmodified S molecule from 4. Are they enantiomers or are they model with the identical? Draw the mirror image of this stereoisomer and assign the R/S configurations of each chiral carbons for both isomers. 6. Shown below is the Fisher projection of (R)-2-bromo-(S)-3-chlorobutane. CH3 -Br CH3 CI H. mirror plane 7. Make models of both stereoisomers in question 6. Test the models for superimposability. Secure the initials of your TA after showing them your physical model of (R)-2-bromo-(S)-3-chlorobutane. initials In the space below draw Fisher projections of the two stereoisomers of 2- thich are diastereomers of the stereoisomers shown in nnstructed for question 7 and switch two del represented by one of the mmetric centers.
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