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

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
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### Reaction Problem 

#### Instructions:
Draw the product of the reaction shown below. Ignore inorganic byproducts.

#### Reaction Details:
- **Starting Material:**
  - Structure: Contains a benzene ring fused to a cyclohexene ring, with a propyl group attached.
- **Reagents:**
  1. KMnO₄, H₂O, heat
  2. H⁺ (workup)

#### Diagram:
- There is a placeholder labeled "Drawing" which indicates where the drawn product should be placed.

### Explanation:
The reaction involves the oxidation of the alkyl side chain on an aromatic ring using potassium permanganate (KMnO₄) as the oxidizing agent. The typical outcome is the conversion of alkyl side chains to carboxylic acids. 

Upon heating with KMnO₄ in water, followed by acidic workup, the propyl group attached to the aromatic structure will likely be oxidized to a carboxylic acid.
Transcribed Image Text:### Reaction Problem #### Instructions: Draw the product of the reaction shown below. Ignore inorganic byproducts. #### Reaction Details: - **Starting Material:** - Structure: Contains a benzene ring fused to a cyclohexene ring, with a propyl group attached. - **Reagents:** 1. KMnO₄, H₂O, heat 2. H⁺ (workup) #### Diagram: - There is a placeholder labeled "Drawing" which indicates where the drawn product should be placed. ### Explanation: The reaction involves the oxidation of the alkyl side chain on an aromatic ring using potassium permanganate (KMnO₄) as the oxidizing agent. The typical outcome is the conversion of alkyl side chains to carboxylic acids. Upon heating with KMnO₄ in water, followed by acidic workup, the propyl group attached to the aromatic structure will likely be oxidized to a carboxylic acid.
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