Draw the major organic product(s) of the following reaction. CH3 C=C-H NaNH2 , NH3(1) CH3-I • You do not have to consider stereochemistry. Separate multiple products using the + sign from the drop-down menu. If no reaction occurs, draw the organic starting material.

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**Title: Organic Chemistry Reaction**

**Objective:**

Draw the major organic product(s) of the following reaction.

**Reaction Details:**

Chemical reaction:
- Starting material: Cycloalkyne with methyl substituent
- Reagents: NaNH₂ / NH₃(l)
- Followed by: CH₃I

![Chemical Reaction Diagram]
The diagram shows a cycloalkyne with a terminal alkyne group. It undergoes reaction with sodium amide (NaNH₂) in liquid ammonia (NH₃(l)). This is followed by the addition of methyl iodide (CH₃I), resulting in alkylation at the terminal carbon.

**Guidelines:**

- No need to consider stereochemistry.
- Separate multiple products using the "+" sign from the drop-down menu.
- If no reaction occurs, draw the organic starting material.

**Instructions:**

Analyze the reaction mechanism and predict the product(s). Consider the role of the reagents in deprotonating and alkylating the alkyne.
Transcribed Image Text:**Title: Organic Chemistry Reaction** **Objective:** Draw the major organic product(s) of the following reaction. **Reaction Details:** Chemical reaction: - Starting material: Cycloalkyne with methyl substituent - Reagents: NaNH₂ / NH₃(l) - Followed by: CH₃I ![Chemical Reaction Diagram] The diagram shows a cycloalkyne with a terminal alkyne group. It undergoes reaction with sodium amide (NaNH₂) in liquid ammonia (NH₃(l)). This is followed by the addition of methyl iodide (CH₃I), resulting in alkylation at the terminal carbon. **Guidelines:** - No need to consider stereochemistry. - Separate multiple products using the "+" sign from the drop-down menu. - If no reaction occurs, draw the organic starting material. **Instructions:** Analyze the reaction mechanism and predict the product(s). Consider the role of the reagents in deprotonating and alkylating the alkyne.
**Reaction Product Description:**

**Reaction:**
The given reaction involves the oxidation of an alkene compound using potassium permanganate (KMnO₄) in acidic conditions (H₃O⁺).

**Structure of Reactant:**
The reactant is a benzene ring bonded to an alkyne group (-C≡C-) that is further connected to a long-chain alcohol (HO-C(CH₂)₅-).

**Instructions for Drawing the Product(s):**

- **Stereochemistry:** No need to consider stereochemistry when drawing the products.
  
- **Multiple Compounds:** If the same compound is formed more than once, use an additional sketcher to represent it.
  
- **Carbon Dioxide:** If carbon dioxide is a reaction product, draw it separately.
  
- **Product Separation:** Use the '+' sign from the drop-down menu to separate multiple reaction products.
  
- **No Reaction Outcome:** If the reaction does not occur, redraw the original starting material.

In this reaction, traditional oxidative cleavage reactions usually result in the breakdown of C≡C bonds with the formation of carboxylic acids or ketones and possibly the release of carbon dioxide if terminal alkynes are involved or if complete oxidation occurs.
Transcribed Image Text:**Reaction Product Description:** **Reaction:** The given reaction involves the oxidation of an alkene compound using potassium permanganate (KMnO₄) in acidic conditions (H₃O⁺). **Structure of Reactant:** The reactant is a benzene ring bonded to an alkyne group (-C≡C-) that is further connected to a long-chain alcohol (HO-C(CH₂)₅-). **Instructions for Drawing the Product(s):** - **Stereochemistry:** No need to consider stereochemistry when drawing the products. - **Multiple Compounds:** If the same compound is formed more than once, use an additional sketcher to represent it. - **Carbon Dioxide:** If carbon dioxide is a reaction product, draw it separately. - **Product Separation:** Use the '+' sign from the drop-down menu to separate multiple reaction products. - **No Reaction Outcome:** If the reaction does not occur, redraw the original starting material. In this reaction, traditional oxidative cleavage reactions usually result in the breakdown of C≡C bonds with the formation of carboxylic acids or ketones and possibly the release of carbon dioxide if terminal alkynes are involved or if complete oxidation occurs.
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