DE 1. В-Н6, diglyme 2. NaOH, H-O, Н2О2

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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In the given image, an educational chemistry interface is displayed. The task is to "Draw the organic product structure formed by the reaction sequence."

### Reaction Sequence
1. The starting compound is a cyclohexene, which is a six-membered ring with one double bond.
2. The first reagent is \( \text{B}_2\text{H}_6 \) in diglyme.
3. The second step involves \( \text{NaOH}, \text{H}_2\text{O}, \) and \( \text{H}_2\text{O}_2 \).

### Explanation of Reaction
This sequence of reagents typically describes hydroboration-oxidation. In this process:
- **Step 1:** \( \text{B}_2\text{H}_6 \) adds across the double bond of cyclohexene to form an organoborane intermediate.
- **Step 2:** The organoborane intermediate is then treated with \( \text{NaOH}, \text{H}_2\text{O}, \) and \( \text{H}_2\text{O}_2 \) to yield an alcohol. 

Hydroboration-oxidation gives anti-Markovnikov addition, resulting in the formation of an alcohol where the hydroxyl group attaches to the less substituted carbon of the original double bond.

### Diagram Area
- A drawing interface allows users to sketch the structure of the product.
- Options for selecting different drawing tools and elements like "Rings," "C," "H," "O," and more are available.
- The "Erase" button is provided for corrections.

### User Interface
- A button labeled "Draw the Product" is prominently displayed for input.
- Undo and redo buttons allow navigation through drawing steps.

This setup is used to engage students in learning reaction mechanisms by visualizing the outcome of organic transformations.
Transcribed Image Text:In the given image, an educational chemistry interface is displayed. The task is to "Draw the organic product structure formed by the reaction sequence." ### Reaction Sequence 1. The starting compound is a cyclohexene, which is a six-membered ring with one double bond. 2. The first reagent is \( \text{B}_2\text{H}_6 \) in diglyme. 3. The second step involves \( \text{NaOH}, \text{H}_2\text{O}, \) and \( \text{H}_2\text{O}_2 \). ### Explanation of Reaction This sequence of reagents typically describes hydroboration-oxidation. In this process: - **Step 1:** \( \text{B}_2\text{H}_6 \) adds across the double bond of cyclohexene to form an organoborane intermediate. - **Step 2:** The organoborane intermediate is then treated with \( \text{NaOH}, \text{H}_2\text{O}, \) and \( \text{H}_2\text{O}_2 \) to yield an alcohol. Hydroboration-oxidation gives anti-Markovnikov addition, resulting in the formation of an alcohol where the hydroxyl group attaches to the less substituted carbon of the original double bond. ### Diagram Area - A drawing interface allows users to sketch the structure of the product. - Options for selecting different drawing tools and elements like "Rings," "C," "H," "O," and more are available. - The "Erase" button is provided for corrections. ### User Interface - A button labeled "Draw the Product" is prominently displayed for input. - Undo and redo buttons allow navigation through drawing steps. This setup is used to engage students in learning reaction mechanisms by visualizing the outcome of organic transformations.
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