Provide an answer for each in the space provided. 1. Provide a structure for the major product of each reaction. Be sure to include relative stereochemistry if it is pertinent CH3 1. TSCI, EtN 2. NaOCH3 DMF, 100 °C H3C 'CH3 он H2 (1 atm) cat. [Pd] H.

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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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**Problem Statement:**

Provide an answer for each in the space provided.

1. Provide a structure for the **major product** of each reaction. Be sure to include relative stereochemistry if it is pertinent.

**Chemical Reactions:**

- **Reaction 1:**
  - **Starting Material:** A cyclohexane ring with an OH group and two methyl groups attached.
  - **Reagents:**
    1. TsCl (p-Toluenesulfonyl chloride), Et₃N (Triethylamine)
    2. NaOCH₃, DMF (Dimethylformamide), 100°C
  - **Process:**
    - The reaction likely involves the conversion of the hydroxyl group (OH) to a tosylate group by TsCl and Et₃N, followed by nucleophilic substitution with NaOCH₃ to form an ether.
    
- **Reaction 2:**
  - **Starting Material:** A bicyclic compound with a ketone (C=O) and a double bond.
  - **Reagents:** H₂ (1 atm), catalytic Pd (palladium catalyst)
  - **Process:**
    - This reaction involves hydrogenation, where the double bond is reduced to a single bond in the presence of H₂ and a palladium catalyst.
Transcribed Image Text:**Problem Statement:** Provide an answer for each in the space provided. 1. Provide a structure for the **major product** of each reaction. Be sure to include relative stereochemistry if it is pertinent. **Chemical Reactions:** - **Reaction 1:** - **Starting Material:** A cyclohexane ring with an OH group and two methyl groups attached. - **Reagents:** 1. TsCl (p-Toluenesulfonyl chloride), Et₃N (Triethylamine) 2. NaOCH₃, DMF (Dimethylformamide), 100°C - **Process:** - The reaction likely involves the conversion of the hydroxyl group (OH) to a tosylate group by TsCl and Et₃N, followed by nucleophilic substitution with NaOCH₃ to form an ether. - **Reaction 2:** - **Starting Material:** A bicyclic compound with a ketone (C=O) and a double bond. - **Reagents:** H₂ (1 atm), catalytic Pd (palladium catalyst) - **Process:** - This reaction involves hydrogenation, where the double bond is reduced to a single bond in the presence of H₂ and a palladium catalyst.
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