Draw the major product of this reaction. Ignore inorganic byproducts.

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Draw the major product of this reaction. Ignore inorganic byproducts.

**Transcription and Explanation:**

**Chemical Structure:**
The image displays a chemical structure of a benzene ring, which is a hexagonal ring composed of six carbon atoms with alternating double bonds, commonly represented as a hexagon with lines inside it indicating double bonds.

**Chemical Reaction Steps:**

1. **Ozone (O₃) Reaction:**
   - The first step involves the introduction of ozone (O₃), a molecule consisting of three oxygen atoms. This indicates the process of ozonolysis, which is used to break down alkenes into carbonyl compounds.

2. **Dimethyl Sulfide (CH₃SCH₃) Reaction:**
   - The second step involves the use of dimethyl sulfide (CH₃SCH₃). This suggests a reductive workup, which is often used to cleave ozonides formed during ozonolysis into aldehydes or ketones.

**Educational Context:**
This reaction sequence illustrates how ozonolysis, followed by a reductive workup, can be used to cleave unsaturated hydrocarbon rings like benzene, converting them into simpler compounds. This is a common technique studied in organic chemistry for modifying and analyzing the structure of organic molecules.
Transcribed Image Text:**Transcription and Explanation:** **Chemical Structure:** The image displays a chemical structure of a benzene ring, which is a hexagonal ring composed of six carbon atoms with alternating double bonds, commonly represented as a hexagon with lines inside it indicating double bonds. **Chemical Reaction Steps:** 1. **Ozone (O₃) Reaction:** - The first step involves the introduction of ozone (O₃), a molecule consisting of three oxygen atoms. This indicates the process of ozonolysis, which is used to break down alkenes into carbonyl compounds. 2. **Dimethyl Sulfide (CH₃SCH₃) Reaction:** - The second step involves the use of dimethyl sulfide (CH₃SCH₃). This suggests a reductive workup, which is often used to cleave ozonides formed during ozonolysis into aldehydes or ketones. **Educational Context:** This reaction sequence illustrates how ozonolysis, followed by a reductive workup, can be used to cleave unsaturated hydrocarbon rings like benzene, converting them into simpler compounds. This is a common technique studied in organic chemistry for modifying and analyzing the structure of organic molecules.
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