Choose the best reagent from the list below for carrying out each transformation. Place the letter of the reagent in the blank to the left of the reaction. a. b. 1. 03 2. Zn, H₂O* 1. BH3, THF 2. H₂O2, NaOH, H₂O c. CHCl3, KOH d. H₂O, H₂SO4, heat . CH₂ CH3 e. 1. Os04 2. NaHSO3, H₂O f. KMnO4, acid g. CH₂I2, Zn(Cu) h. 1. Hg(OAc)2, H₂O 2. NaBH₁ Н. CH3 OH CH₂

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**Title: Organic Chemistry Reagents and Transformations**

**Instructions:**
Choose the best reagent from the list below for carrying out each transformation. Place the letter of the reagent in the blank to the left of the reaction.

**Reagent Options:**
- a.  
  1. \( \text{O}_3 \)  
  2. \(\text{Zn, H}_3\text{O}^+\)
- b.  
  1. \(\text{BH}_3, \; \text{THF}\)  
  2. \(\text{H}_2\text{O}_2, \; \text{NaOH, H}_2\text{O}\)
- c. \(\text{CHCl}_3, \; \text{KOH}\)
- d. \(\text{H}_2\text{O, H}_2\text{SO}_4, \; \text{heat}\)
- e.  
  1. \(\text{OsO}_4\)  
  2. \(\text{NaHSO}_3, \; \text{H}_2\text{O}\)
- f. \(\text{KMnO}_4, \; \text{acid}\)
- g. \(\text{CH}_2\text{I}_2, \; \text{Zn(Cu)}\)
- h.
  1. \(\text{Hg(OAc)}_2, \; \text{H}_2\text{O}\)  
  2. \(\text{NaBH}_4\)

**Reactions:**

1. **Reaction 1:**
   - **Starting Material:** Cyclohexene with a methyl group branching.
   - **Product:** Cyclohexanol with a methyl group branching.

2. **Reaction 2:**
   - **Starting Material:** Cyclohexene with a methyl group branching.
   - **Product:** A linear diketone with methyl and propyl chains on either side of two carbonyl groups.

**Diagram Explanation:**

- **First Diagram:** Displays the transformation of an alkene (cyclohexene) to an alcohol through the addition of an -OH group, maintaining the carbon ring structure and methyl branch.
  
- **Second Diagram:** Represents the oxidation of an alkene leading to cleavage
Transcribed Image Text:**Title: Organic Chemistry Reagents and Transformations** **Instructions:** Choose the best reagent from the list below for carrying out each transformation. Place the letter of the reagent in the blank to the left of the reaction. **Reagent Options:** - a. 1. \( \text{O}_3 \) 2. \(\text{Zn, H}_3\text{O}^+\) - b. 1. \(\text{BH}_3, \; \text{THF}\) 2. \(\text{H}_2\text{O}_2, \; \text{NaOH, H}_2\text{O}\) - c. \(\text{CHCl}_3, \; \text{KOH}\) - d. \(\text{H}_2\text{O, H}_2\text{SO}_4, \; \text{heat}\) - e. 1. \(\text{OsO}_4\) 2. \(\text{NaHSO}_3, \; \text{H}_2\text{O}\) - f. \(\text{KMnO}_4, \; \text{acid}\) - g. \(\text{CH}_2\text{I}_2, \; \text{Zn(Cu)}\) - h. 1. \(\text{Hg(OAc)}_2, \; \text{H}_2\text{O}\) 2. \(\text{NaBH}_4\) **Reactions:** 1. **Reaction 1:** - **Starting Material:** Cyclohexene with a methyl group branching. - **Product:** Cyclohexanol with a methyl group branching. 2. **Reaction 2:** - **Starting Material:** Cyclohexene with a methyl group branching. - **Product:** A linear diketone with methyl and propyl chains on either side of two carbonyl groups. **Diagram Explanation:** - **First Diagram:** Displays the transformation of an alkene (cyclohexene) to an alcohol through the addition of an -OH group, maintaining the carbon ring structure and methyl branch. - **Second Diagram:** Represents the oxidation of an alkene leading to cleavage
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