2. Carefully draw the structures of the models that you have made using proper stereochemical notation. The mirror images should be drawn side-by-side indicating the mirror plane. Structures should be drawn using the zig-zag style, either by hand or using ChemDraw 3. Determine if the mirror images can be superposed and therefore if they are enantiomers and/or diastereomers. 4. Identify the stereogenic centre(s) of the molecule. Dotorn 00Gonia gonto (P
2. Carefully draw the structures of the models that you have made using proper stereochemical notation. The mirror images should be drawn side-by-side indicating the mirror plane. Structures should be drawn using the zig-zag style, either by hand or using ChemDraw 3. Determine if the mirror images can be superposed and therefore if they are enantiomers and/or diastereomers. 4. Identify the stereogenic centre(s) of the molecule. Dotorn 00Gonia gonto (P
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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
Transcribed Image Text:2. Carefully draw the structures of the models that you have made using proper
stereochemical notation. The mirror images should be drawn side-by-side indicating the
mirror plane. Structures should be drawn using the zig-zag style, either by hand or using
ChemDraw
3. Determine if the mirror images can be superposed and therefore if they are enantiomers
and/or diastereomers.
4. Identify the stereogenic centre(s) of the molecule.
5. Determine the configuration at each stereogenic centre (R or S).
6. For compounds that have more than one stereogenic centre, prepare all the possible
stereoisomers of the compound, including all mirror images. You should try to prepare all
of the isomers of a given compound at the same time.
7. Carefully draw the models that you have made using proper stereochemical notation. The
mirror images should be drawn side-by-side indicating the mirror plane. Models should be
drawn using the zig-zag style.
8. If there are more than 2 stereoisomers, perform a full stereochemical analysis of your
structures, indicating which pairs are enantiomers and/or diastereomers. Identify the
stereogenic centre(s) of the molecule and determine the configuration at each stereogenic
centre.

Transcribed Image Text:CH3CH(NH2)CO2H
CH3CH2CH(Br)CH(CH3)OH
| C
А
В
CH(CH2CH3)(CH3)2
HOCH2CH(OH)CH(OH)CH2OH
D
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