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6. Shown below is the Fisher projection of (R)-2-bromo-(S)-3-chlorobutane. Draw the mirror image of this stereoisomer and assign the R/S configurations of each chiral carbons for both isomers. H CH3 CH3 H H -Br -CI 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 8. In the space below draw Fisher projections of the two stereoisomers of 2- bromo-3-chlorobutane which are diastereomers of the stereoisomers shown in question 6. Take one of the models constructed for question 7 and switch two groups around one of the chiral carbons. Is this model represented by one of the Fisher projections you drew below? Indicate R and S for all asymmetric centers.

6. Shown below is the Fisher projection of (R)-2-bromo-(S)-3-chlorobutane. Draw the mirror image of this stereoisomer and assign the R/S configurations of each chiral carbons for both isomers. H CH3 CH3 H H -Br -CI 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 8. In the space below draw Fisher projections of the two stereoisomers of 2- bromo-3-chlorobutane which are diastereomers of the stereoisomers shown in question 6. Take one of the models constructed for question 7 and switch two groups around one of the chiral carbons. Is this model represented by one of the Fisher projections you drew below? Indicate R and S for all asymmetric centers.

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Please answer questions 6, 7, and 8. They are all related to each other. Please write neatly, answer and label all parts, and circle answers.
Now switch any pair of groups around the chiral carbon of the "switched" model again! Compare the "double-switched" model with the other unmodified S molecule from 4. Are they enantiomers or are they identical? 6. Shown below is the Fisher projection of (R)-2-bromo-(S)-3-chlorobutane. Draw the mirror image of this stereoisomer and assign the R/S configurations of each chiral carbons for both isomers. CH3 CH3 8. H H Br -CI 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- bromo-3-chlorobutane which are diastereomers of the stereoisomers shown in question 6. Take one of the models constructed for question 7 and switch two groups around one of the chiral carbons. Is this model represented by one of the Fisher projections you drew below? Indicate R and S for all asymmetric centers. 8
Transcribed Image Text:Now switch any pair of groups around the chiral carbon of the "switched" model again! Compare the "double-switched" model with the other unmodified S molecule from 4. Are they enantiomers or are they identical? 6. Shown below is the Fisher projection of (R)-2-bromo-(S)-3-chlorobutane. Draw the mirror image of this stereoisomer and assign the R/S configurations of each chiral carbons for both isomers. CH3 CH3 8. H H Br -CI 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- bromo-3-chlorobutane which are diastereomers of the stereoisomers shown in question 6. Take one of the models constructed for question 7 and switch two groups around one of the chiral carbons. Is this model represented by one of the Fisher projections you drew below? Indicate R and S for all asymmetric centers. 8
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