Draw the major product formed when the given epoxide reacts with aqueous acid. Select Draw Rings H3O* H2O

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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**Task: Epoxide Reaction with Aqueous Acid**

**Objective:** Draw the major product formed when the given epoxide reacts with aqueous acid.

**Chemical Structure:**
- The image shows a cyclic epoxide with two carbon atoms and one oxygen atom in the ring. 
- It has a methyl group (CH₃) and a hydrogen atom (H) attached to one of the carbons in the ring.
  
**Reaction Conditions:**
- Reacting with hydronium ion (H₃O⁺) in water (H₂O).

**Instructions for Drawing:**
- Utilize the drawing tools provided: single, double, and triple bond options, as well as options to add carbon, hydrogen, and oxygen atoms.
- Use the workspace on the right to draw the major product.

**Considerations:**
- Epoxides open up when reacted with acids.
- Assess regioselectivity and stereochemistry based on the starting material and conditions provided. 

**Note:** The goal is to apply knowledge of organic reaction mechanisms, particularly focusing on the acid-catalyzed opening of epoxides.
Transcribed Image Text:**Task: Epoxide Reaction with Aqueous Acid** **Objective:** Draw the major product formed when the given epoxide reacts with aqueous acid. **Chemical Structure:** - The image shows a cyclic epoxide with two carbon atoms and one oxygen atom in the ring. - It has a methyl group (CH₃) and a hydrogen atom (H) attached to one of the carbons in the ring. **Reaction Conditions:** - Reacting with hydronium ion (H₃O⁺) in water (H₂O). **Instructions for Drawing:** - Utilize the drawing tools provided: single, double, and triple bond options, as well as options to add carbon, hydrogen, and oxygen atoms. - Use the workspace on the right to draw the major product. **Considerations:** - Epoxides open up when reacted with acids. - Assess regioselectivity and stereochemistry based on the starting material and conditions provided. **Note:** The goal is to apply knowledge of organic reaction mechanisms, particularly focusing on the acid-catalyzed opening of epoxides.
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