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Organic Chemistry I |
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Professor Carl C. Wamser |
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Chapter 7 Notes |
Stereochemistry
Enantiomers
Enantiomer Examples
Chirality
Stereogenic Centers
Identifying Chiral Molecules
Optical Activity
Specific Rotation
Absolute Configuration
R and S Designations
Right- and Left-Hand Views
Drawing 3-D Structures
Fischer Projections
Multiple Stereogenic Centers
Diastereomers
Meso Compounds
Identifying Meso Compounds
Cyclohexane Derivatives
Configurations and Conformations of Disubstituted Cyclohexanes
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(R,S) interconverting enantiomers |
(R,R) & (S,S) isolable enantiomers two conformations each |
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isolable enantiomers two conformations each |
isolable enantiomers two conformations each |
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(R,S) - meso compound two conformations |
isolable enantiomers two conformations each |
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isolable enantiomers two conformations each |
isolable enantiomers two conformations each |
no stereocenters |
equivalent conformations |
two conformations |
no stereocenters |
two conformations |
two conformations |
Racemic Mixtures
Optical Purity / Enantiomeric Excess
Optical Resolution
Isomerism - Summary
Stereoisomers - Summary
Reactions involving stereoisomers