| Sections | |||
|---|---|---|---|
| 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 |
|---|
| Racemic Mixture |
| Achiral |
Determine whether the two structures in each of the following pairs represent constitutional isomers, different conformations of the same compound, or stereoisomers that cannot be interconverted by rotation about single bonds.
(d) cis-1,2-Dimethylcyclopentane and trans-1,3-dimethylcyclopentane
Enter your friends' email addresses to invite them:
Join thousands of students and gain free access to 63 hours of Organic videos that follow the topics your textbook covers.