The R and S enantiomers of an optically active compound differ in:
1. Their optical rotation of plane-polarized light.
2. Their reactivity with chiral reagents.
3. Their solubility in achiral reagents.
4. Their melting points.

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The most stable conformation of n-butane among the following is:
| 1. | 2. | ||
| 3. | 4. |

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What is the relationship between the two given molecular structures?

| 1. | Enantiomers | 2. | Position isomers |
| 3. | Conformers | 4. | None of the above |

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