1. 2. OH 1. + 2. OCH 3 Na NH₂ a Proton transfer b = Lewis acid/base c = Radical chain substitution AIBN 70⁰ + O Na CO₂CH3 H₂ to²-ct CH3 poly(methyl methacrylate) (Plexiglass, Lucite) NH3 d = Radical chain addition e = Electrophilic addition f = E1 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i for your answers. g= E2 Elimination h = SN1 Nucleophilic substitution i = SN2 Nucleophilic substitution
1. 2. OH 1. + 2. OCH 3 Na NH₂ a Proton transfer b = Lewis acid/base c = Radical chain substitution AIBN 70⁰ + O Na CO₂CH3 H₂ to²-ct CH3 poly(methyl methacrylate) (Plexiglass, Lucite) NH3 d = Radical chain addition e = Electrophilic addition f = E1 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i for your answers. g= E2 Elimination h = SN1 Nucleophilic substitution i = 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 Mechanism Identification
1. **Reaction 1:**
- **Equation:**
- Organic compound with -OH group reacts with sodium amide (NaNH₂) to produce a compound with a carbon-carbon double bond and ammonia (NH₃).
2. **Reaction 2:**
- **Equation:**
- An ester compound undergoes a reaction in the presence of AIBN at 70°C to form poly(methyl methacrylate), commonly known as Plexiglass or Lucite.
### Mechanism Options:
- **a =** Proton transfer
- **b =** Lewis acid/base
- **c =** Radical chain substitution
- **d =** Radical chain addition
- **e =** Electrophilic addition
- **f =** E1 Elimination
- **g =** E2 Elimination
- **h =** Sₙ1 Nucleophilic substitution
- **i =** Sₙ2 Nucleophilic substitution
### Instructions:
Identify the mechanism by which each of the reactions proceeds from among the mechanisms listed. Use the letters a - i for your answers.
1. **Reaction 1: [ ]**
2. **Reaction 2: [ ]**](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F4f7442e5-ed1a-4154-ba5d-4813abad6cff%2F2e8aa7f2-bc1a-4237-9ffb-2127ea61cf3a%2Fptqfc7q_processed.png&w=3840&q=75)
Transcribed Image Text:### Reaction Mechanism Identification
1. **Reaction 1:**
- **Equation:**
- Organic compound with -OH group reacts with sodium amide (NaNH₂) to produce a compound with a carbon-carbon double bond and ammonia (NH₃).
2. **Reaction 2:**
- **Equation:**
- An ester compound undergoes a reaction in the presence of AIBN at 70°C to form poly(methyl methacrylate), commonly known as Plexiglass or Lucite.
### Mechanism Options:
- **a =** Proton transfer
- **b =** Lewis acid/base
- **c =** Radical chain substitution
- **d =** Radical chain addition
- **e =** Electrophilic addition
- **f =** E1 Elimination
- **g =** E2 Elimination
- **h =** Sₙ1 Nucleophilic substitution
- **i =** Sₙ2 Nucleophilic substitution
### Instructions:
Identify the mechanism by which each of the reactions proceeds from among the mechanisms listed. Use the letters a - i for your answers.
1. **Reaction 1: [ ]**
2. **Reaction 2: [ ]**
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Given are organic reactions.
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