1. KMNO4, HO¯, heat 2. H3O*

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Please draw the correct aromatic organic product for the following reaction

### Oxidation of Alkyl Benzene using Potassium Permanganate

**Reaction Overview:**

This reaction involves the oxidation of an alkyl benzene using potassium permanganate (KMnO₄) under basic conditions with heat, followed by acidification.

1. **Reagents and Conditions:**
   - **Step 1:** Potassium permanganate (KMnO₄), hydroxide ions (HO⁻), and heat
   - **Step 2:** Acidic workup using hydronium ions (H₃O⁺)

**Chemical Structure:**

- **Starting Material:** An alkyl benzene with the alkyl group being an isopropyl group (a benzene ring attached to a CH-(CH₃)₂ group).
- The benzene ring is a six-carbon ring with alternating double bonds, representing the aromatic nature of benzene.

**Reaction Process:**

- **Step 1:** The alkyl side chain of the benzene is oxidized by KMnO₄ in the presence of a base (HO⁻) and heat. This process typically leads to the conversion of the entire alkyl chain into a carboxylic acid group.
- **Step 2:** The acidic workup (H₃O⁺) neutralizes the reaction mixture and may be used to ensure the complete formation of the carboxylic acid product.

**Mechanism Insight:**

- **Oxidation:** The powerful oxidizing agent KMnO₄ breaks down the alkyl side chain, while the basic environment facilitates the removal of hydrogen atoms, leading to the formation of a carboxylate intermediate.
- **Acidification:** The carboxylate ion is protonated to form the carboxylic acid in the final step.

This reaction is commonly employed to convert alkyl benzenes into benzoic acids through oxidative conditions, demonstrating the versatility of benzene ring chemistry and the robustness of permanganate as an oxidizing agent.
Transcribed Image Text:### Oxidation of Alkyl Benzene using Potassium Permanganate **Reaction Overview:** This reaction involves the oxidation of an alkyl benzene using potassium permanganate (KMnO₄) under basic conditions with heat, followed by acidification. 1. **Reagents and Conditions:** - **Step 1:** Potassium permanganate (KMnO₄), hydroxide ions (HO⁻), and heat - **Step 2:** Acidic workup using hydronium ions (H₃O⁺) **Chemical Structure:** - **Starting Material:** An alkyl benzene with the alkyl group being an isopropyl group (a benzene ring attached to a CH-(CH₃)₂ group). - The benzene ring is a six-carbon ring with alternating double bonds, representing the aromatic nature of benzene. **Reaction Process:** - **Step 1:** The alkyl side chain of the benzene is oxidized by KMnO₄ in the presence of a base (HO⁻) and heat. This process typically leads to the conversion of the entire alkyl chain into a carboxylic acid group. - **Step 2:** The acidic workup (H₃O⁺) neutralizes the reaction mixture and may be used to ensure the complete formation of the carboxylic acid product. **Mechanism Insight:** - **Oxidation:** The powerful oxidizing agent KMnO₄ breaks down the alkyl side chain, while the basic environment facilitates the removal of hydrogen atoms, leading to the formation of a carboxylate intermediate. - **Acidification:** The carboxylate ion is protonated to form the carboxylic acid in the final step. This reaction is commonly employed to convert alkyl benzenes into benzoic acids through oxidative conditions, demonstrating the versatility of benzene ring chemistry and the robustness of permanganate as an oxidizing agent.
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