The following molecules are subject to substitution (SN1 or SN2) reaction conditions. a) Identify if the leaving group (-Br) is attached to a 3°, 2°, 1°, or methyl Carbon. b) Rank the molecule with respect to their SN1 reactivity, with 1 being the fastest and 4 being the slowest. c) Rank the molecule with respect to their SN2 reactivity, with 1 being the fastest and 4 being the slowest. Br Br CH3B Br a. type of Carbon on C-Br b. SN1 reactivity (1 fastest, 4 slowest) c. SN2 reactivity (1 fastest, 4 slowest)
The following molecules are subject to substitution (SN1 or SN2) reaction conditions. a) Identify if the leaving group (-Br) is attached to a 3°, 2°, 1°, or methyl Carbon. b) Rank the molecule with respect to their SN1 reactivity, with 1 being the fastest and 4 being the slowest. c) Rank the molecule with respect to their SN2 reactivity, with 1 being the fastest and 4 being the slowest. Br Br CH3B Br a. type of Carbon on C-Br b. SN1 reactivity (1 fastest, 4 slowest) c. SN2 reactivity (1 fastest, 4 slowest)
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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 (**Isopropyl Bromide**)
3.  (**1-Bromopropane**)
4.  (**Tert-butyl Bromide**)
#### Tasks:
a) **Identify if the leaving group (-Br) is attached to a 3°, 2°, 1°, or methyl Carbon.**
b) **Rank the molecule with respect to their SN1 reactivity, with 1 being the fastest and 4 being the slowest.**
c) **Rank the molecule with respect to their SN2 reactivity, with 1 being the fastest and 4 being the slowest.**
#### Template for Filling In:
| | CH₃Br | Isopropyl Bromide | 1-Bromopropane | Tert-butyl Bromide |
|------------------|-------------|-------------------------|----------------------|-------------------------|
| **a. type of Carbon on C-Br** | ___________ | ___________ | ___________ | ___________ |
| **b. SN1 reactivity (1 fastest, 4 slowest)** | ___________ | ___________ | ___________ | ___________ |
| **c. SN2 reactivity (1 fastest, 4 slowest)** | ___________ | ___________ | ___________ | ___________ |
#### Additional Notes:
- **Methyl Carbon**](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F30c2e2f2-e45c-41de-86ef-a25e36084e76%2F51a0923d-607b-4cea-80d6-65325071db64%2Fn6sa46.jpeg&w=3840&q=75)
Transcribed Image Text:### Substitution Reaction Analysis: SN1 and SN2
The following molecules are subject to substitution (SN1 or SN2) reaction conditions.
#### Molecule Structures
1. **CH₃Br**
2.  (**Isopropyl Bromide**)
3.  (**1-Bromopropane**)
4.  (**Tert-butyl Bromide**)
#### Tasks:
a) **Identify if the leaving group (-Br) is attached to a 3°, 2°, 1°, or methyl Carbon.**
b) **Rank the molecule with respect to their SN1 reactivity, with 1 being the fastest and 4 being the slowest.**
c) **Rank the molecule with respect to their SN2 reactivity, with 1 being the fastest and 4 being the slowest.**
#### Template for Filling In:
| | CH₃Br | Isopropyl Bromide | 1-Bromopropane | Tert-butyl Bromide |
|------------------|-------------|-------------------------|----------------------|-------------------------|
| **a. type of Carbon on C-Br** | ___________ | ___________ | ___________ | ___________ |
| **b. SN1 reactivity (1 fastest, 4 slowest)** | ___________ | ___________ | ___________ | ___________ |
| **c. SN2 reactivity (1 fastest, 4 slowest)** | ___________ | ___________ | ___________ | ___________ |
#### Additional Notes:
- **Methyl Carbon**
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