3.) For each of the following reactions, please draw the main product(s), and indicate if the reaction should go via E1, E2, SN1, and/or SN2 mechanism(s) and why. For eliminations, indicate Zaitsev or Hoffman as applicable. Make sure to include stereochemistry where appropriate. 3a.) 3b.) CI CH3OH (CH3)3COK >

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**Exercise 3**

For each of the following reactions, please draw the main product(s) and indicate if the reaction should go via E1, E2, Sn1, and/or Sn2 mechanism(s) and why. For eliminations, indicate Zaitsev or Hoffman as applicable. Make sure to include stereochemistry where appropriate.

**3a.**

- Structure: Cyclopentane ring with a chlorine atom attached to a carbon. The chlorine is in a wedge position (indicating a certain stereochemistry).
- Reagent: Methanol (\(CH_3OH\)).

**3b.**

- Structure: Cyclohexane ring with a chlorine atom and a tertiary butyl group attached to a same carbon. The chlorine is in a wedge position.
- Reagent: Potassium tert-butoxide \((CH_3)_3COK\).
Transcribed Image Text:**Exercise 3** For each of the following reactions, please draw the main product(s) and indicate if the reaction should go via E1, E2, Sn1, and/or Sn2 mechanism(s) and why. For eliminations, indicate Zaitsev or Hoffman as applicable. Make sure to include stereochemistry where appropriate. **3a.** - Structure: Cyclopentane ring with a chlorine atom attached to a carbon. The chlorine is in a wedge position (indicating a certain stereochemistry). - Reagent: Methanol (\(CH_3OH\)). **3b.** - Structure: Cyclohexane ring with a chlorine atom and a tertiary butyl group attached to a same carbon. The chlorine is in a wedge position. - Reagent: Potassium tert-butoxide \((CH_3)_3COK\).
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