
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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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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