Organic Chemistry (9th Edition)
Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
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Chapter 15.6, Problem 15.8P

When Br2 is added to buta-1,3-diene at −15 °C, the product mixture contains 60% of product A and 40% of product B. When the same reaction takes place at 60 °C, the product ratio is 10% A and 90% B.

  1. a. Propose structures for products A and B. (Hint: In many cases, an allylic carbocation is more stable than a bromonium ion.)
  2. b. Propose a mechanism to account for formation of both A and B.
  3. c. Show why A predominates at −15 °C and B predominates at 60 °C.
  4. d. If you had a solution of pure A, and its temperature were raised to 60 °C, what would you expect to happen? Propose a mechanism to support your prediction.
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1. An alkyl chloride is treated with lithium diisopropyl amide, forming the following two products. Determine the structure of the starting material and identify which of the two products is favored. What is the mechanism of this reaction? 2. Predict the major product for each of the following reactions, all of which use the same starting material. Show stereochemistry where relevant. 1. OsO4 2. TBUOOH 1 BH. THE
Why do cis-1-bromo-2-ethylcyclohexane and trans-1-bromo-2-ethylcyclohexane form different major products when they undergo an E2 reaction?

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