### Transcription of Diagram Instructions:Modify the structures in the box below to complete the drawing of the enantiomer of \((R)-(+)-\text{thalidomide}\).---### Diagram Explanation:The image displays a chemical structure of thalidomide. Key features include:- **A benzene ring** on the left, identifiable by a hexagonal shape with alternating double bonds.- **Two carbonyl groups (C=O)** are present, each attached to different nitrogen atoms within the bicyclic structure.- **A chiral center** is depicted with a wedge bond indicating stereochemistry, crucial for differentiating enantiomers.- **An imide group** is also visible, connecting to both rings through nitrogen atoms.The task likely involves altering the stereochemistry at the chiral center to achieve the specified enantiomer.---**Note:** The text "5th attempt" suggests this is the fifth time the student is trying to modify the structure.

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Answered: Modify the structures in the box below…

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Chemistry

Modify the structures in the box below to complete the drawing of the enantiomer of (R)-(+)-thalidomide.

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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Question

### Transcription of Diagram Instructions:

Modify the structures in the box below to complete the drawing of the enantiomer of \((R)-(+)-\text{thalidomide}\).

---

### Diagram Explanation:

The image displays a chemical structure of thalidomide. Key features include:

- **A benzene ring** on the left, identifiable by a hexagonal shape with alternating double bonds.
- **Two carbonyl groups (C=O)** are present, each attached to different nitrogen atoms within the bicyclic structure.
- **A chiral center** is depicted with a wedge bond indicating stereochemistry, crucial for differentiating enantiomers.
- **An imide group** is also visible, connecting to both rings through nitrogen atoms.

The task likely involves altering the stereochemistry at the chiral center to achieve the specified enantiomer.

---

**Note:** The text "5th attempt" suggests this is the fifth time the student is trying to modify the structure.

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