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
Draw the product of the reaction shown below. Ignore
inorganic byproducts.

Transcribed Image Text:**Title: Understanding Oxidation Reactions in Organic Chemistry**
**Exercise:**
Draw the product of the reaction shown below. Ignore inorganic byproducts.
**Chemical Structure:**
- A five-membered cyclopentene ring with one double bond.
- There are two hydroxyl (OH) groups attached to the cyclopentene, one on either carbon adjacent to the double bond.
**Reagents:**
- Na₂Cr₂O₇ (Sodium dichromate)
- H₂O (Water)
- CH₃CO₂H (Acetic acid)
**Explanation:**
In this reaction, a cyclopentene diol undergoes oxidation in the presence of sodium dichromate in an aqueous acetic acid solution. The hydroxyl groups are potential sites of oxidation, and the target product will be a ketone or carboxylic acid depending on specific conditions. This setup is a classic example of Jones oxidation conditions commonly used to transform alcohols into carbonyl groups.
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