ОН ОН ОН ОН ОН ОН OH OH

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Identify the unique pairs of enantiomers and find any diastereomers. 

The image shows four structural representations of a chemical compound with chiral centers, indicating different stereoisomers. Each structure has a carbon chain with two hydroxyl (OH) groups attached.

1. **First Structure**:
   - Both hydroxyl groups are in the "up" position, indicated by bold wedges. This means both chiral centers have an R or S configuration that directs the OH groups towards the same side.

2. **Second Structure**:
   - The first hydroxyl group is in the "up" position (bold wedge), while the second is in the "down" position (dashed wedge). This indicates an opposite configuration at the second chiral center compared to the first.

3. **Third Structure**:
   - Both hydroxyl groups are in the "down" position, represented by dashed wedges. This symmetry suggests opposite stereochemistry at each chiral center compared to the first structure.

4. **Fourth Structure**:
   - The first hydroxyl group is in the "down" position (dashed wedge), and the second is in the "up" position (bold wedge), showing an opposite configuration at the first chiral center compared to the second structure.

These variations demonstrate different stereoisomers of the compound, highlighting the importance of spatial arrangement in chiral molecules.
Transcribed Image Text:The image shows four structural representations of a chemical compound with chiral centers, indicating different stereoisomers. Each structure has a carbon chain with two hydroxyl (OH) groups attached. 1. **First Structure**: - Both hydroxyl groups are in the "up" position, indicated by bold wedges. This means both chiral centers have an R or S configuration that directs the OH groups towards the same side. 2. **Second Structure**: - The first hydroxyl group is in the "up" position (bold wedge), while the second is in the "down" position (dashed wedge). This indicates an opposite configuration at the second chiral center compared to the first. 3. **Third Structure**: - Both hydroxyl groups are in the "down" position, represented by dashed wedges. This symmetry suggests opposite stereochemistry at each chiral center compared to the first structure. 4. **Fourth Structure**: - The first hydroxyl group is in the "down" position (dashed wedge), and the second is in the "up" position (bold wedge), showing an opposite configuration at the first chiral center compared to the second structure. These variations demonstrate different stereoisomers of the compound, highlighting the importance of spatial arrangement in chiral molecules.
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