**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 \((CH_3)_3COK\).

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 >

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 >

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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