he alkenes shown below, which would product the product shown below, upon treatment with ozone (03), d by zinc metal (Zn) and acetic acid? que ??? II III IV

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**Transcription for Educational Website:**

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**Question (xi):** Of the alkenes shown below, which would produce the product shown below, upon treatment with ozone (O₃), followed by zinc metal (Zn) and acetic acid?

**Reaction Scheme:**
- ??? → [Arrow pointing to the right] 

**Product Structure:**
- The chemical structure shown is an aldehyde, specifically hexanal (OHC-C4H8-CO).

**Alkene Options:**
1. **Structure I:** 
   - Cyclohexene (a six-membered carbon ring with one double bond).

2. **Structure II:** 
   - Cycloheptene (a seven-membered carbon ring with one double bond).

3. **Structure III:** 
   - Cyclooctene (an eight-membered carbon ring with one double bond).

4. **Structure IV:** 
   - A cyclobutene derivative (four-membered carbon ring with one double bond and an ethyl group attached).

---

**Explanation:**

The question involves determining which alkene, upon undergoing ozonolysis, followed by reductive workup, would yield the given aldehyde structure. 

Ozonolysis is a reaction where ozone cleaves double bonds in alkenes to form carbonyl compounds. Reductive workup with zinc and acetic acid typically converts the resulting ozonides into aldehydes and/or ketones.
Transcribed Image Text:**Transcription for Educational Website:** --- **Question (xi):** Of the alkenes shown below, which would produce the product shown below, upon treatment with ozone (O₃), followed by zinc metal (Zn) and acetic acid? **Reaction Scheme:** - ??? → [Arrow pointing to the right] **Product Structure:** - The chemical structure shown is an aldehyde, specifically hexanal (OHC-C4H8-CO). **Alkene Options:** 1. **Structure I:** - Cyclohexene (a six-membered carbon ring with one double bond). 2. **Structure II:** - Cycloheptene (a seven-membered carbon ring with one double bond). 3. **Structure III:** - Cyclooctene (an eight-membered carbon ring with one double bond). 4. **Structure IV:** - A cyclobutene derivative (four-membered carbon ring with one double bond and an ethyl group attached). --- **Explanation:** The question involves determining which alkene, upon undergoing ozonolysis, followed by reductive workup, would yield the given aldehyde structure. Ozonolysis is a reaction where ozone cleaves double bonds in alkenes to form carbonyl compounds. Reductive workup with zinc and acetic acid typically converts the resulting ozonides into aldehydes and/or ketones.
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