Draw a curved arrow mechanism for the reaction, adding steps as necessary. Be sure to include all electrons that are necessary to the mechanism and all nonzero formal charges. C™ H C + Add/Remove step +40-to X H H

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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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Draw a curved arrow mechanism for the reaction, adding steps as necessary. Be sure to include all electrons that are necessary to the mechanism and all nonzero formal charges.

I did the first step but I'm not sure if it's correct. Don't know what the other steps, if there are, would look like.
 

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
**Curved Arrow Mechanism for the Reaction**

**Objective:**
Draw a curved arrow mechanism for the reaction, including necessary steps. Ensure all electrons required for the mechanism and nonzero formal charges are shown.

**Description:**

In the given reaction mechanism, we have the following components:

1. **Starting Materials on the Left:**

   - An alcohol group (isopropanol derivative) with a hydroxyl group (–OH) attached to a tertiary carbon.
   - A sulfonic acid derivative with a sulfonate ester group (–SO₃).

2. **Mechanism Step:**

   - The lone pair of electrons on the oxygen of the hydroxyl group attacks the hydrogen atom, forming a curved arrow. This interaction leads to the formation of an oxonium ion intermediate, which has a positive charge on the oxygen (O⁺).

3. **Products on the Right:**

   - The protonated alcohol is shown with a positively charged oxygen.
   - The sulfonic acid residue remains with a stable structure.

**Curved Arrows:**

- The curved arrow from the lone pair on the oxygen to the hydrogen indicates the nucleophilic attack.
- The resulting positive charge on the alcohol's oxygen is highlighted.

This diagram underscores the shift of electrons and formation of intermediates during the reaction process.
Transcribed Image Text:**Curved Arrow Mechanism for the Reaction** **Objective:** Draw a curved arrow mechanism for the reaction, including necessary steps. Ensure all electrons required for the mechanism and nonzero formal charges are shown. **Description:** In the given reaction mechanism, we have the following components: 1. **Starting Materials on the Left:** - An alcohol group (isopropanol derivative) with a hydroxyl group (–OH) attached to a tertiary carbon. - A sulfonic acid derivative with a sulfonate ester group (–SO₃). 2. **Mechanism Step:** - The lone pair of electrons on the oxygen of the hydroxyl group attacks the hydrogen atom, forming a curved arrow. This interaction leads to the formation of an oxonium ion intermediate, which has a positive charge on the oxygen (O⁺). 3. **Products on the Right:** - The protonated alcohol is shown with a positively charged oxygen. - The sulfonic acid residue remains with a stable structure. **Curved Arrows:** - The curved arrow from the lone pair on the oxygen to the hydrogen indicates the nucleophilic attack. - The resulting positive charge on the alcohol's oxygen is highlighted. This diagram underscores the shift of electrons and formation of intermediates during the reaction process.
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