1. 2. OH 1. "CI 2. CH3 a Proton transfer b = Lewis acid/base c = Electrophilic addition 1. BBr3 heat 2. H₂O NaOH CH₂Br B(OH)3 NaCl d = E1 Elimination e = E2 Elimination The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a-g for your answers. f = SN1 Nucleophilic substitution g= SN2 Nucleophilic substitution
1. 2. OH 1. "CI 2. CH3 a Proton transfer b = Lewis acid/base c = Electrophilic addition 1. BBr3 heat 2. H₂O NaOH CH₂Br B(OH)3 NaCl d = E1 Elimination e = E2 Elimination The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a-g for your answers. f = SN1 Nucleophilic substitution g= SN2 Nucleophilic substitution
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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![### Reaction Mechanisms of Alcohols and Ethers
#### Reactions:
1. **Reaction 1**:
- Starting Material: Contains a benzene ring with a methyl group (CH₃).
- Reagents: 1. BBr₃, heat 2. H₂O
- Products: A phenol (benzene ring with an OH group), CH₃Br, and B(OH)₃.
2. **Reaction 2**:
- Starting Material: Cyclohexanol with a chlorine group, reacting with NaOH.
- Product: The OH group forms part of a cyclic ether, and NaCl is produced.
#### Mechanisms:
- **a** = Proton transfer
- **b** = Lewis acid/base
- **c** = Electrophilic addition
- **d** = E1 Elimination
- **e** = E2 Elimination
- **f** = S_N1 Nucleophilic substitution
- **g** = S_N2 Nucleophilic substitution
#### Instructions:
The reactions above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters **a - g** for your answers.
1. [ ]
2. [ ]](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ff6fb7511-1856-448d-bebf-6dbc22fbc7f8%2F81879af6-2acc-4c28-bc91-47a4ea8ce393%2Fb64up6_processed.png&w=3840&q=75)
Transcribed Image Text:### Reaction Mechanisms of Alcohols and Ethers
#### Reactions:
1. **Reaction 1**:
- Starting Material: Contains a benzene ring with a methyl group (CH₃).
- Reagents: 1. BBr₃, heat 2. H₂O
- Products: A phenol (benzene ring with an OH group), CH₃Br, and B(OH)₃.
2. **Reaction 2**:
- Starting Material: Cyclohexanol with a chlorine group, reacting with NaOH.
- Product: The OH group forms part of a cyclic ether, and NaCl is produced.
#### Mechanisms:
- **a** = Proton transfer
- **b** = Lewis acid/base
- **c** = Electrophilic addition
- **d** = E1 Elimination
- **e** = E2 Elimination
- **f** = S_N1 Nucleophilic substitution
- **g** = S_N2 Nucleophilic substitution
#### Instructions:
The reactions above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters **a - g** for your answers.
1. [ ]
2. [ ]
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