7.68 Answer:

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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I don't understand how these are enantiomers. I know that enantiomers are mirror images of each other, but these don't look mirrored.

The image presents a problem related to organic chemistry, specifically focusing on stereochemistry.

### Description:

**Main Content:**

- **Molecules:**
  - The image shows two cyclohexane molecules with various substituents indicated by solid and dashed wedges. These represent different spatial orientations (stereochemistry) of the substituents.

- **Numbering and Labels:**
  - A number "7.68" is shown, likely indicating the problem number or question reference.
  - There is a label "Answer:" followed by a blank space for the solution.

**Diagrams:**

- **Left Molecule:**
  - Shows a cyclohexane ring with three substituents. The orientation and position of these substituents are important for determining stereochemistry (e.g., axial or equatorial).

- **Right Molecule:**
  - Similarly, displays a cyclohexane ring with three substituents. The diagram uses wedges to indicate whether each substituent is positioned above or below the plane of the ring.

### Educational Focus:

- **Stereochemistry:**
  - The use of wedges helps illustrate the three-dimensional structure of molecules. Solid wedges indicate substituents coming out of the plane, while dashed wedges indicate substituents going behind the plane.

- **Axial vs. Equatorial:**
  - Understanding the difference between axial and equatorial positions on a cyclohexane ring is crucial for predicting molecular stability and reactions.

This problem likely involves determining the relationship between the given structures, such as identifying them as stereoisomers, and analyzing their spatial arrangement.
Transcribed Image Text:The image presents a problem related to organic chemistry, specifically focusing on stereochemistry. ### Description: **Main Content:** - **Molecules:** - The image shows two cyclohexane molecules with various substituents indicated by solid and dashed wedges. These represent different spatial orientations (stereochemistry) of the substituents. - **Numbering and Labels:** - A number "7.68" is shown, likely indicating the problem number or question reference. - There is a label "Answer:" followed by a blank space for the solution. **Diagrams:** - **Left Molecule:** - Shows a cyclohexane ring with three substituents. The orientation and position of these substituents are important for determining stereochemistry (e.g., axial or equatorial). - **Right Molecule:** - Similarly, displays a cyclohexane ring with three substituents. The diagram uses wedges to indicate whether each substituent is positioned above or below the plane of the ring. ### Educational Focus: - **Stereochemistry:** - The use of wedges helps illustrate the three-dimensional structure of molecules. Solid wedges indicate substituents coming out of the plane, while dashed wedges indicate substituents going behind the plane. - **Axial vs. Equatorial:** - Understanding the difference between axial and equatorial positions on a cyclohexane ring is crucial for predicting molecular stability and reactions. This problem likely involves determining the relationship between the given structures, such as identifying them as stereoisomers, and analyzing their spatial arrangement.
Expert Solution
Step 1

We are given two structures and are to discuss if they are enantiomers or not.

Enantiomers are two structures which are mirror images of each other.

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