4. What is the expected product of the following reaction? A) OCH 3 B) OH CH 3 C) CH3OH H+ OCH 3 D) O CH3 OH

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### Question 4: Reaction Product Prediction

**4. What is the expected product of the following reaction?**

The reaction involves an oxirane (a three-membered cyclic ether) reacting with methanol (CH₃OH) in the presence of an acid (H⁺). The task is to determine which one of the given options (A, B, C, or D) accurately represents the product formed from this reaction.

The given options are:

- **A)** ![Option A](https://example.com/structureA.svg)
  - Structure: A five-membered cyclic ether with a methoxy (-OCH₃) group attached to the ring.
  
- **B)** ![Option B](https://example.com/structureB.svg)
  - Structure: A five-membered cyclic ether with a hydroxyl (-OH) group and a methyl (CH₃) group attached to the ring.
  
- **C)** ![Option C](https://example.com/structureC.svg)
  - Structure: A five-membered cyclic ether with a methoxy (-OCH₃) group and a methyl group (CH₃) attached to the ring.
  
- **D)** ![Option D](https://example.com/structureD.svg)
  - Structure: A five-membered cyclic ether with a hydroxyl (-OH) group and a methyl group (CH₃) attached to the ring.

To solve this question, one must apply knowledge of organic chemistry reaction mechanisms, particularly the acid-catalyzed opening of epoxides and subsequent nucleophilic attack by methanol.

The correct answer should show the ring opened with the groups resulting from the nucleophilic attack by CH₃OH in the presence of H⁺ (acid).
Transcribed Image Text:### Question 4: Reaction Product Prediction **4. What is the expected product of the following reaction?** The reaction involves an oxirane (a three-membered cyclic ether) reacting with methanol (CH₃OH) in the presence of an acid (H⁺). The task is to determine which one of the given options (A, B, C, or D) accurately represents the product formed from this reaction. The given options are: - **A)** ![Option A](https://example.com/structureA.svg) - Structure: A five-membered cyclic ether with a methoxy (-OCH₃) group attached to the ring. - **B)** ![Option B](https://example.com/structureB.svg) - Structure: A five-membered cyclic ether with a hydroxyl (-OH) group and a methyl (CH₃) group attached to the ring. - **C)** ![Option C](https://example.com/structureC.svg) - Structure: A five-membered cyclic ether with a methoxy (-OCH₃) group and a methyl group (CH₃) attached to the ring. - **D)** ![Option D](https://example.com/structureD.svg) - Structure: A five-membered cyclic ether with a hydroxyl (-OH) group and a methyl group (CH₃) attached to the ring. To solve this question, one must apply knowledge of organic chemistry reaction mechanisms, particularly the acid-catalyzed opening of epoxides and subsequent nucleophilic attack by methanol. The correct answer should show the ring opened with the groups resulting from the nucleophilic attack by CH₃OH in the presence of H⁺ (acid).
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