A. Construct two models of 1-bromo-1-chloroethane. Test to see if the two models are superimposable on one another. If they are superimposable, change the position of Br and Cl on one model. Now you have two models that are not superimposable. These two are enantiomers, non-superimposable mirror image isomers. (Turn, twist, rotate, do anything that you want to these models except interchange the positions of the groups; they remain non-superimposable.) Position these enantiomers so that they appear as mirror images. Arrange them so that the Br is on top and the CH3 is on the bottom of the chiral carbon atom, and the H and Cl are coming out of the plane toward you. Now draw the projection formulas for these enantiomers. Br

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter12: Chirality
Section: Chapter Questions
Problem 5CTQ
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A. Construct two models of 1-bromo-1-chloroethane. Test to see if the two models are
superimposable on one another. If they are superimposable, change the position of Br
and Cl on one model. Now you have two models that are not superimposable. These
two are enantiomers, non-superimposable mirror image isomers. (Turn, twist, rotate,
do anything that you want to these models except interchange the positions of the
groups; they remain non-superimposable.) Position these enantiomers so that they
appear as mirror images. Arrange them so that the Br is on top and the CH3 is on
the bottom of the chiral carbon atom, and the H and Cl are coming out of the plane
toward you. Now draw the projection formulas for these enantiomers.
Br
Transcribed Image Text:A. Construct two models of 1-bromo-1-chloroethane. Test to see if the two models are superimposable on one another. If they are superimposable, change the position of Br and Cl on one model. Now you have two models that are not superimposable. These two are enantiomers, non-superimposable mirror image isomers. (Turn, twist, rotate, do anything that you want to these models except interchange the positions of the groups; they remain non-superimposable.) Position these enantiomers so that they appear as mirror images. Arrange them so that the Br is on top and the CH3 is on the bottom of the chiral carbon atom, and the H and Cl are coming out of the plane toward you. Now draw the projection formulas for these enantiomers. Br
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