What is (are) the expected major product(s) for the following reaction sequence? enantiomer ||| OI and II O II I OI and III ΟΙ OH 1. BH₂-THF 2. H₂O₂, NaOH enantiomer II OH 8.1. enantiomer III 25 nts

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Question 34
**Question:**

What is (are) the expected *major* product(s) for the following reaction sequence?

**Reaction Sequence:**

1. \( \text{BH}_3 \cdot \text{THF} \)
2. \( \text{H}_2 \text{O}_2 \), \( \text{NaOH} \)

**Possible Major Products:**

- **I**
  - A molecular structure displaying a hydroxyl group attached to a carbon on a skeletal formula + enantiomer.
  
- **II**
  - A molecular structure displaying a hydroxyl group attached to a different carbon on a skeletal formula + enantiomer.
  
- **III**
  - A molecular structure displaying a hydroxyl group attached to yet another different carbon on a skeletal formula + enantiomer.

**Answer Choices:**

- ☐ III
- ☐ I and II
- ☐ II
- ☐ I and III
- ☐ I

**Explanation:**

- The reaction sequence involves the hydroboration-oxidation of an alkene, which typically results in the addition of a hydroxyl group (OH) to the less substituted carbon of the alkene.
- Enantiomers are pairs of molecules that are mirror images of each other but are not identical. The + enantiomer notation indicates that each product shown has a corresponding enantiomer.

**Diagrams Explanation:**

- **Diagram for I:**
  - Shows the molecular structure with an OH group attached to the second carbon of a pentane backbone.
- **Diagram for II:**
  - Illustrates the structure with the OH group attached to the third carbon of the pentane backbone.
- **Diagram for III:**
  - Displays the structure with the OH group attached to the fourth carbon of the pentane backbone.

This content forms part of a chemistry educational module explaining the results of hydroboration-oxidation reactions and the concept of enantiomers in organic chemistry.
Transcribed Image Text:**Question:** What is (are) the expected *major* product(s) for the following reaction sequence? **Reaction Sequence:** 1. \( \text{BH}_3 \cdot \text{THF} \) 2. \( \text{H}_2 \text{O}_2 \), \( \text{NaOH} \) **Possible Major Products:** - **I** - A molecular structure displaying a hydroxyl group attached to a carbon on a skeletal formula + enantiomer. - **II** - A molecular structure displaying a hydroxyl group attached to a different carbon on a skeletal formula + enantiomer. - **III** - A molecular structure displaying a hydroxyl group attached to yet another different carbon on a skeletal formula + enantiomer. **Answer Choices:** - ☐ III - ☐ I and II - ☐ II - ☐ I and III - ☐ I **Explanation:** - The reaction sequence involves the hydroboration-oxidation of an alkene, which typically results in the addition of a hydroxyl group (OH) to the less substituted carbon of the alkene. - Enantiomers are pairs of molecules that are mirror images of each other but are not identical. The + enantiomer notation indicates that each product shown has a corresponding enantiomer. **Diagrams Explanation:** - **Diagram for I:** - Shows the molecular structure with an OH group attached to the second carbon of a pentane backbone. - **Diagram for II:** - Illustrates the structure with the OH group attached to the third carbon of the pentane backbone. - **Diagram for III:** - Displays the structure with the OH group attached to the fourth carbon of the pentane backbone. This content forms part of a chemistry educational module explaining the results of hydroboration-oxidation reactions and the concept of enantiomers in organic chemistry.
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