Fill in the missing products for when the following molecules are reacted with various reagents.

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
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Fill in the missing products for when the following molecules are reacted with various reagents.

The image shows a chemical transformation diagram involving a hexose molecule. The structure of the hexose is labeled with carbon numbers (1 through 6) and displays hydroxyl groups (OH) attached to each carbon.

- **Reagents and Reaction Conditions:**
  - An arrow pointing upwards is labeled with two reagents:
    1. SOCl₂ (thionyl chloride)
    2. COONa (sodium carboxylate)
  
- **Additional Information:**
  - To the left of the hexose structure, "PCC" (pyridinium chlorochromate) is noted, often used for oxidation in organic chemistry.
  - To the right of the structure, "Jones" is mentioned, referring to Jones oxidation, a method using chromium trioxide (CrO₃) in sulfuric acid, which oxidizes alcohols to carboxylic acids.
  
This setup likely represents a proposed synthetic pathway involving oxidation and substitution reactions to modify the hydroxyl groups on the hexose ring.
Transcribed Image Text:The image shows a chemical transformation diagram involving a hexose molecule. The structure of the hexose is labeled with carbon numbers (1 through 6) and displays hydroxyl groups (OH) attached to each carbon. - **Reagents and Reaction Conditions:** - An arrow pointing upwards is labeled with two reagents: 1. SOCl₂ (thionyl chloride) 2. COONa (sodium carboxylate) - **Additional Information:** - To the left of the hexose structure, "PCC" (pyridinium chlorochromate) is noted, often used for oxidation in organic chemistry. - To the right of the structure, "Jones" is mentioned, referring to Jones oxidation, a method using chromium trioxide (CrO₃) in sulfuric acid, which oxidizes alcohols to carboxylic acids. This setup likely represents a proposed synthetic pathway involving oxidation and substitution reactions to modify the hydroxyl groups on the hexose ring.
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