OMe ? Me OMe ОН

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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Which reaction sequence would provide the following transformation?
**Chemical Reaction Pathway: Introduction to Synthetic Organic Chemistry**

In this example, we are exploring the synthetic pathway for modifying a benzene ring with a methoxy group (OMe) into a more complex organic molecule.

**Starting Material:**
- The starting molecule is a benzene ring with a single methoxy group attached to one of the carbon atoms. The methoxy group (OMe) is attached to the top of the benzene ring.

**Product:**
- The resulting product is a benzene ring substituted with a methoxy group (OMe) at the same position as the starting material. Additionally, the following modifications are made:
  - There is a side chain containing a double bond (an alkene) attached to the carbon adjacent to the carbon with the methoxy group.
  - Another side chain that contains a hydroxyl group (OH) and a methyl group (Me) is attached to the carbon adjacent to the other side of the carbon with the methoxy group. Specifically, the arrangement of OH and Me indicates a secondary alcohol.

This synthetic transformation demonstrates functional group additions and modifications to the aromatic ring, a common theme in organic synthesis to build up molecular complexity. 

**Graphical Description of the Reaction Scheme:**
- On the far left, the starting material, anisole (methoxybenzene), is represented. 
- An arrow points to the right, indicating a chemical transformation.
- A question mark above the arrow suggests unspecified reagents, which facilitate the transformation. 
- On the right side of the arrow, the product is shown. 

Understanding how to modify benzene rings with various functional groups is fundamental in organic chemistry, and this example represents a practical application of these concepts in synthesizing complex organic molecules.
Transcribed Image Text:**Chemical Reaction Pathway: Introduction to Synthetic Organic Chemistry** In this example, we are exploring the synthetic pathway for modifying a benzene ring with a methoxy group (OMe) into a more complex organic molecule. **Starting Material:** - The starting molecule is a benzene ring with a single methoxy group attached to one of the carbon atoms. The methoxy group (OMe) is attached to the top of the benzene ring. **Product:** - The resulting product is a benzene ring substituted with a methoxy group (OMe) at the same position as the starting material. Additionally, the following modifications are made: - There is a side chain containing a double bond (an alkene) attached to the carbon adjacent to the carbon with the methoxy group. - Another side chain that contains a hydroxyl group (OH) and a methyl group (Me) is attached to the carbon adjacent to the other side of the carbon with the methoxy group. Specifically, the arrangement of OH and Me indicates a secondary alcohol. This synthetic transformation demonstrates functional group additions and modifications to the aromatic ring, a common theme in organic synthesis to build up molecular complexity. **Graphical Description of the Reaction Scheme:** - On the far left, the starting material, anisole (methoxybenzene), is represented. - An arrow points to the right, indicating a chemical transformation. - A question mark above the arrow suggests unspecified reagents, which facilitate the transformation. - On the right side of the arrow, the product is shown. Understanding how to modify benzene rings with various functional groups is fundamental in organic chemistry, and this example represents a practical application of these concepts in synthesizing complex organic molecules.
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