When the halohydrin is treated with NaH, a product of molecular formula C4H8O is formed. Draw the structure of the product and indicate its stereochemistry. CI CH3 H OH H CH3

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Click the "draw structure" button to launch the drawing utility.

When the halohydrin is treated with NaH, a product of molecular formula C₄H₈O is formed. Draw the structure of the product and indicate its stereochemistry.

**Image Descriptions:**

1. **Structural Formula:**
   - Two carbon atoms are connected by a single bond.
   - The first carbon atom (on the left) is bonded to a chlorine atom (Cl) and a methyl group (CH₃). 
   - The second carbon atom (on the right) is bonded to a hydroxyl group (OH) and a methyl group (CH₃).
   - Stereochemistry is indicated by bold and dashed bonds, showing the three-dimensional arrangement of groups.

2. **Edited Structure:**
   - A central carbon atom is bonded to a hydrogen atom (H), two methyl groups (CH₃), and an oxygen atom (O).
   - The stereochemistry is also indicated by bold and dashed bonds.

In the context of the reaction, the transformation involves creating an epoxide from a halohydrin using sodium hydride (NaH).
Transcribed Image Text:Click the "draw structure" button to launch the drawing utility. When the halohydrin is treated with NaH, a product of molecular formula C₄H₈O is formed. Draw the structure of the product and indicate its stereochemistry. **Image Descriptions:** 1. **Structural Formula:** - Two carbon atoms are connected by a single bond. - The first carbon atom (on the left) is bonded to a chlorine atom (Cl) and a methyl group (CH₃). - The second carbon atom (on the right) is bonded to a hydroxyl group (OH) and a methyl group (CH₃). - Stereochemistry is indicated by bold and dashed bonds, showing the three-dimensional arrangement of groups. 2. **Edited Structure:** - A central carbon atom is bonded to a hydrogen atom (H), two methyl groups (CH₃), and an oxygen atom (O). - The stereochemistry is also indicated by bold and dashed bonds. In the context of the reaction, the transformation involves creating an epoxide from a halohydrin using sodium hydride (NaH).
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