**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.

In E2 elemination leaving group and adjacent hydrogen must be anti-periplaner

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.

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.

Chemistry

10th Edition

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

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Question

**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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