Analyze the following reaction mechanisms. How many bond forming events occur in this mechanism? OH tzt. t t Acetone (CH3COCH 3) Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a b с Three Two Four d One :OH O.. :OH

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**Analyze the following reaction mechanisms. How many bond forming events occur in this mechanism?**

**Diagram Explanation:**
The reaction mechanism involves acetone (CH₃COCH₃) undergoing interactions with water (H₂O). The image shows a step-by-step transformation with electron movements depicted by curved arrows, indicating bond formation and breakage. Here’s a breakdown:

1. **First Step:** Acetone interacts with a water molecule. The lone pair on oxygen from the water attacks the carbonyl carbon of acetone, leading to the formation of a tetrahedral intermediate.

2. **Second Step:** A proton shift occurs, illustrating the basic interaction between the oxygen atoms and hydrogen.

3. **Third Step:** Final stabilization involves the movement of electrons, resulting in a stable molecule with an eliminated hydroxide ion (OH⁻).

**Question:**
Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer.

- a. Three
- b. Two
- c. Four
- d. One
Transcribed Image Text:**Analyze the following reaction mechanisms. How many bond forming events occur in this mechanism?** **Diagram Explanation:** The reaction mechanism involves acetone (CH₃COCH₃) undergoing interactions with water (H₂O). The image shows a step-by-step transformation with electron movements depicted by curved arrows, indicating bond formation and breakage. Here’s a breakdown: 1. **First Step:** Acetone interacts with a water molecule. The lone pair on oxygen from the water attacks the carbonyl carbon of acetone, leading to the formation of a tetrahedral intermediate. 2. **Second Step:** A proton shift occurs, illustrating the basic interaction between the oxygen atoms and hydrogen. 3. **Third Step:** Final stabilization involves the movement of electrons, resulting in a stable molecule with an eliminated hydroxide ion (OH⁻). **Question:** Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. - a. Three - b. Two - c. Four - d. One
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