Chapter 11: 40E (page 350)
The following Walden cycle has been carried out. Explain the results, and indicate where Walden inversion occurs.

Short Answer
Inversion takes place in step 4.step4

Walden Inversion
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Chapter 11: 40E (page 350)
The following Walden cycle has been carried out. Explain the results, and indicate where Walden inversion occurs.

Inversion takes place in step 4.step4

Walden Inversion
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Which isomer would you expect to undergo E2 elimination faster, trans-1-bromo-4-tert-butylcyclohexane or cis-1-bromo-4-tert-butylcyclohexane? Draw each molecule in its more stable chair conformation, and explain your answer.
(S)-2-Butanol slowly racemizes on standing in dilute sulfuric acid. Explain.

Amines are converted into alkenes by a two-step process called Hofmann elimination. SN2 reaction of the amine with an excess of in the first step yields an intermediate that undergoes E2reaction when treated with silver oxide as base. Pentylamine, for example, yields 1-pentene. Propose a structure for the intermediate, and explain why it readily undergoes elimination.
Question: Predict the major alkene product of the following E1 reaction:

Draw the structure and assign Z or E stereochemistry to the product you expect from E2 reaction of the following molecule with NaOH (green = Cl):

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