Draw the major product of this reaction. Ignore inorganic byproducts and CO2. 1. O3 2. Zn, HOAC

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Draw the major products of this reaction 

Title: Understanding Ozonolysis Reaction

---

**Reaction Overview:**

The question asks to identify the major product formed from the given organic reaction, specifically focusing on an alkene undergoing ozonolysis. The reagents involved are:

1. **Ozone (O₃)**: Used for breaking the carbon-carbon double bond.
2. **Zinc and Acetic Acid (Zn, HOAc)**: Utilized to reduce the ozonide intermediate, leading to the formation of carbonyl compounds.

**Given Structure:**

The starting molecule is a branched alkene. It is important to recognize the functional groups and the structure:

- **Skeleton Description**: The molecule contains a branched chain with a double bond.
- **Key Group**: The presence of the alkene's double bond is the target for the ozonolysis.

**Steps in Reaction:**

1. **Ozonolysis**: The double bond in the alkene reacts with ozone to form a cyclic ozonide.
2. **Reduction**: The addition of zinc and acetic acid breaks down the ozonide, leading to the formation of aldehydes or ketones from each end of the original double bond.

**Expected Major Product:**

The reaction will yield two carbonyl compounds (usually aldehydes and ketones). The structure of these products will depend on the original positioning of the carbon chain and double bond.

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This reaction is a classic example of how alkenes can be cleaved to form useful carbonyl-containing compounds, illustrating the utility of ozonolysis in organic synthesis. By studying the structural transformation, students can better predict reaction outcomes and understand the mechanistic pathways involved.
Transcribed Image Text:Title: Understanding Ozonolysis Reaction --- **Reaction Overview:** The question asks to identify the major product formed from the given organic reaction, specifically focusing on an alkene undergoing ozonolysis. The reagents involved are: 1. **Ozone (O₃)**: Used for breaking the carbon-carbon double bond. 2. **Zinc and Acetic Acid (Zn, HOAc)**: Utilized to reduce the ozonide intermediate, leading to the formation of carbonyl compounds. **Given Structure:** The starting molecule is a branched alkene. It is important to recognize the functional groups and the structure: - **Skeleton Description**: The molecule contains a branched chain with a double bond. - **Key Group**: The presence of the alkene's double bond is the target for the ozonolysis. **Steps in Reaction:** 1. **Ozonolysis**: The double bond in the alkene reacts with ozone to form a cyclic ozonide. 2. **Reduction**: The addition of zinc and acetic acid breaks down the ozonide, leading to the formation of aldehydes or ketones from each end of the original double bond. **Expected Major Product:** The reaction will yield two carbonyl compounds (usually aldehydes and ketones). The structure of these products will depend on the original positioning of the carbon chain and double bond. --- This reaction is a classic example of how alkenes can be cleaved to form useful carbonyl-containing compounds, illustrating the utility of ozonolysis in organic synthesis. By studying the structural transformation, students can better predict reaction outcomes and understand the mechanistic pathways involved.
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