Draw the product of the reaction shown below. Ignore inorganic byproducts. HO HO Na2Cr207 H2O, CH3CO2H

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...
icon
Related questions
icon
Concept explainers
Question
Draw the product of the reaction shown below. Ignore inorganic byproducts.
**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.
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.
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps with 2 images

Blurred answer
Knowledge Booster
Aromatic Compounds
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Recommended textbooks for you
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY