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)

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### Substitution Reaction Analysis: SN1 and SN2

The following molecules are subject to substitution (SN1 or SN2) reaction conditions.

#### Molecule Structures
1. **CH₃Br**
2. ![Image might contain: isopropyl bromide](https://user-images.githubusercontent.com/1236147/134529147-d521fc53-cc4c-4e97-8e65-34d207a53ecd.png) (**Isopropyl Bromide**)
3. ![Image might contain: 1-bromopropane](https://user-images.githubusercontent.com/1236147/134529147-d521fc53-cc4c-4e97-8e65-34d207a53ecd.png) (**1-Bromopropane**)
4. ![Image might contain: tert-butyl bromide](https://user-images.githubusercontent.com/1236147/134529147-d521fc53-cc4c-4e97-8e65-34d207a53ecd.png) (**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**
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. ![Image might contain: isopropyl bromide](https://user-images.githubusercontent.com/1236147/134529147-d521fc53-cc4c-4e97-8e65-34d207a53ecd.png) (**Isopropyl Bromide**) 3. ![Image might contain: 1-bromopropane](https://user-images.githubusercontent.com/1236147/134529147-d521fc53-cc4c-4e97-8e65-34d207a53ecd.png) (**1-Bromopropane**) 4. ![Image might contain: tert-butyl bromide](https://user-images.githubusercontent.com/1236147/134529147-d521fc53-cc4c-4e97-8e65-34d207a53ecd.png) (**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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