What alkene is required to synthesize the following compound? H CH3CH2 "CH₂CH₂CH3 H

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What alkene is required to synthesize the following compound?

What other epoxide would be formed?

**Question:** What alkene is required to synthesize the following compound?

**Structure Explanation:**

The diagram illustrates a chemical structure of a carbonyl compound featuring a three-membered ring, known as an epoxide. 

- **Central Atom:** The central atom in the structure is a carbon atom, bonded:
  - Upwards to an oxygen atom, forming part of the epoxide ring.
  - To the right, to another carbon atom which connects to a propyl group (CH₂CH₂CH₃).
  - Downwards, to a hydrogen atom.
  - To the left, to a second carbon forming part of the ethyl group (CH₃CH₂).
  
- **Details:**
  - The oxygen atom is double-bonded to the top carbon atom of the three-membered epoxide ring.
  - The two bonds projecting towards the viewer (indicated by solid wedges) signify the stereochemistry where these substituents are above the plane of the ring.
  
**Objective:**

Determine the alkene precursor that would lead to the formation of this epoxide during a typical epoxidation reaction. The original alkene would have a double bond connecting the carbon atoms that the oxygen bridge of the epoxide is currently attached to.
Transcribed Image Text:**Question:** What alkene is required to synthesize the following compound? **Structure Explanation:** The diagram illustrates a chemical structure of a carbonyl compound featuring a three-membered ring, known as an epoxide. - **Central Atom:** The central atom in the structure is a carbon atom, bonded: - Upwards to an oxygen atom, forming part of the epoxide ring. - To the right, to another carbon atom which connects to a propyl group (CH₂CH₂CH₃). - Downwards, to a hydrogen atom. - To the left, to a second carbon forming part of the ethyl group (CH₃CH₂). - **Details:** - The oxygen atom is double-bonded to the top carbon atom of the three-membered epoxide ring. - The two bonds projecting towards the viewer (indicated by solid wedges) signify the stereochemistry where these substituents are above the plane of the ring. **Objective:** Determine the alkene precursor that would lead to the formation of this epoxide during a typical epoxidation reaction. The original alkene would have a double bond connecting the carbon atoms that the oxygen bridge of the epoxide is currently attached to.
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