Table of Contents
Chapter 5
Types of Isomers (Transparency 79)
Chirality
Tests for Chirality In Molecules
Examples of Chiral Molecules
Examples of Achiral Molecules
Requirements For Enantiomeric Pairs
Biological Importance of Chirality
Physiological Differences Between Enantiomeric Pairs
Physiological Differences Between Enantiomeric Pairs(Continued)
Rules For Establishing R/S Configuration in Enantiomers
Establishing R/S Configuration (continued)
Cahn-Ingold-Prelog Priority Rules
Cahn-Ingold-Prelog Priority Rules (continued)
Properties of Enantiomers
Optical Activity and Configuration
Specific Rotation
Racemates
Enantiomeric Excess
Determination of Stereoisomeric Composition
Determination of Composition(Continued)
Racemization
Enantioselective Reactions
Chiral Drugs
Molecules With Two or More Stereocenters
Meso Forms
Molecules With Two or More Stereocenters (Cont.)
Naming Compounds With Two or More Stereocenters
Naming Compounds With Two or More Stereocenters
Converting 3-D to Fisher Projections
Isomers of dimethylcyclopentane
Retention vs Inversion of Relative Configuration
Relative vs Absolute Configuration
Resolution of Racemic Mixtures
Compounds With Stereocenters Other Than Carbon
Chiral Molecules That Do Not Possess A Tetrahedral Atom With Four Different Groups
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Author: Ralph Logan Jr.
Email: RHL7460@dcccd.edu
Home Page: http://edie.cprost.sfu.ca/~rhlogan
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