03 then ADMO 7

Chemistry
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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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What is the product of this reaction? 

The image displays a chemical reaction scheme. It features the structure of a complex organic molecule that contains a benzene ring and multiple double bonds. The molecule appears to undergo a reaction with ozone (O₃) followed by treatment with DMS (Dimethyl sulfide).

### Reaction Process:

1. **Initial Molecule:** 
   - A linear organic compound comprised of a benzene ring with alternating double bonds extending on either side.

2. **Reagents and Conditions:**
   - **O₃ (Ozone):** This reagent indicates an ozonolysis reaction, which typically involves the cleavage of double bonds.
   - **DMS (Dimethyl sulfide):** A reagent used to further process the ozonide intermediates formed during ozonolysis, often reducing them to form aldehydes or ketones.

3. **Expected Outcome:**
   - The question mark (?) indicates that the final product of the reaction is unknown or is to be determined.

### Explanation:

This reaction is likely a representation of ozonolysis where the goal is to break down the unsaturated compounds (double bonds) in the presence of ozone, often leading to the formation of simpler oxidative products such as aldehydes or ketones using DMS as a reducing agent. The exact transformation and products depend on the initial arrangement of the double bonds. 

This type of reaction is a fundamental topic in organic chemistry, illustrating the alteration of complex organic molecules through cleavage and oxidative processes.
Transcribed Image Text:The image displays a chemical reaction scheme. It features the structure of a complex organic molecule that contains a benzene ring and multiple double bonds. The molecule appears to undergo a reaction with ozone (O₃) followed by treatment with DMS (Dimethyl sulfide). ### Reaction Process: 1. **Initial Molecule:** - A linear organic compound comprised of a benzene ring with alternating double bonds extending on either side. 2. **Reagents and Conditions:** - **O₃ (Ozone):** This reagent indicates an ozonolysis reaction, which typically involves the cleavage of double bonds. - **DMS (Dimethyl sulfide):** A reagent used to further process the ozonide intermediates formed during ozonolysis, often reducing them to form aldehydes or ketones. 3. **Expected Outcome:** - The question mark (?) indicates that the final product of the reaction is unknown or is to be determined. ### Explanation: This reaction is likely a representation of ozonolysis where the goal is to break down the unsaturated compounds (double bonds) in the presence of ozone, often leading to the formation of simpler oxidative products such as aldehydes or ketones using DMS as a reducing agent. The exact transformation and products depend on the initial arrangement of the double bonds. This type of reaction is a fundamental topic in organic chemistry, illustrating the alteration of complex organic molecules through cleavage and oxidative processes.
Expert Solution
Step 1

Ozonolysis: The chemical reaction in which O3(ozone) is used to cleave the double bonds, triple bonds and also azo coupling bonds of the compounds to produce carbonyl compounds.

O3/H2O2 : The H2O2 is an oxidizing agent, hence the resulted aldehyde converts into carboxylic acid when O3/H2O2 reagent is used.

O3/DMS or O3/Zn: The DMS(dimethyl sulfide) or Zn are the reducing agents, hence the ozonolysis only produces aldehydes and ketones.

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