Subjects
Sections | |||
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Constitutional Isomers vs. Stereoisomers | 9 mins | 0 completed | Learn |
Chirality | 12 mins | 0 completed | Learn |
Test 1: Plane of Symmetry | 7 mins | 0 completed | Learn Summary |
Test 2: Stereocenter Test | 17 mins | 0 completed | Learn Summary |
R and S Configuration | 43 mins | 0 completed | Learn Summary |
Enantiomers vs. Diastereomers | 13 mins | 0 completed | Learn |
Atropisomers | 9 mins | 0 completed | Learn |
Meso Compound | 13 mins | 0 completed | Learn Summary |
Test 3: Disubstituted Cycloalkanes | 11 mins | 0 completed | Learn |
What is the Relationship Between Isomers? | 16 mins | 0 completed | Learn Summary |
Fischer Projection | 11 mins | 0 completed | Learn |
R and S of Fischer Projections | 8 mins | 0 completed | Learn |
Optical Activity | 6 mins | 0 completed | Learn |
Enantiomeric Excess | 19 mins | 0 completed | Learn |
Calculations with Enantiomeric Percentages | 12 mins | 0 completed | Learn |
Non-Carbon Chiral Centers | 8 mins | 0 completed | Learn |
Additional Guides |
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Racemic Mixture |
Achiral |
Consider the following pairs of structures. Designate each chirality center as (R) or (S) and identify the relationship between them by describing them as representing enantiomers, diastereomers, constitutional isomers, or two molecules of the same compound. Use handheld molecular models to check your answers.
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