the 3) Write down reactants and/or the reaction conditions, for 10 major products, or the other of the thirteen CH3 A) CH3 + Y OH 111 OH + KMnO4 -> + CH3COOH -->

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Do a c and d listed below
**Organic Chemistry Reactions Exercise**

**Objective:** Write down the major products of the reactions and/or the reaction conditions for the given organic compounds.

**Reactions:**

1. **Reaction A:**
   - Reactants: A benzene ring with a methyl group attached (toluene).
   - Reaction Condition: KMnO₄ (potassium permanganate).
   - Product: The exact product isn't shown, but typically, oxidation of toluene with KMnO₄ can result in benzoic acid.

2. **Reaction B:**
   - Reactants: A six-membered ring with one double bond and a methyl group attached.
   - Reaction Condition: KMnO₄ (potassium permanganate).
   - Product: Not explicitly given, but this usually results in oxidation products due to KMnO₄.

3. **Reaction C:**
   - Reactants: Cyclohexanol.
   - Reaction Condition: KMnO₄ (potassium permanganate).
   - Product: Often results in the conversion of alcohols to acids. In this case, cyclohexanone might be the intermediate or the final product depending on conditions.

4. **Reaction D:**
   - Reactants: Propanol.
   - Reaction Condition: CH₃COOH (acetic acid).
   - Product: This can lead to esterification, producing propyl acetate.

**Note:** These reactions involve transformations where specific reaction conditions lead to the functionalization or modification of organic molecules. Potassium permanganate is frequently used as an oxidizing agent, capable of transforming alcohols into carboxylic acids or ketones. Acetic acid serves as a reagent for esterification reactions.
Transcribed Image Text:**Organic Chemistry Reactions Exercise** **Objective:** Write down the major products of the reactions and/or the reaction conditions for the given organic compounds. **Reactions:** 1. **Reaction A:** - Reactants: A benzene ring with a methyl group attached (toluene). - Reaction Condition: KMnO₄ (potassium permanganate). - Product: The exact product isn't shown, but typically, oxidation of toluene with KMnO₄ can result in benzoic acid. 2. **Reaction B:** - Reactants: A six-membered ring with one double bond and a methyl group attached. - Reaction Condition: KMnO₄ (potassium permanganate). - Product: Not explicitly given, but this usually results in oxidation products due to KMnO₄. 3. **Reaction C:** - Reactants: Cyclohexanol. - Reaction Condition: KMnO₄ (potassium permanganate). - Product: Often results in the conversion of alcohols to acids. In this case, cyclohexanone might be the intermediate or the final product depending on conditions. 4. **Reaction D:** - Reactants: Propanol. - Reaction Condition: CH₃COOH (acetic acid). - Product: This can lead to esterification, producing propyl acetate. **Note:** These reactions involve transformations where specific reaction conditions lead to the functionalization or modification of organic molecules. Potassium permanganate is frequently used as an oxidizing agent, capable of transforming alcohols into carboxylic acids or ketones. Acetic acid serves as a reagent for esterification reactions.
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