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Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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For each of the following, identify the product(s) that would be formed through the indicated sequence of steps from the given starting material.

Transcribed Image Text:(1) Br,
(2) NANH, (3 equiv.),
4, H,O+
(3)
Br
Cul, Pd(Ph,P),
Et,NH
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- 4. Give the mechanism for the following reaction of a Grignard reagent (RMgBr) with diethylcarbonate.arrow_forwardAnother mechanism for the formation of epoxides is through the formation of a chlorohydrin. Alkenes react with chlorine in the presence of H₂O to give a chlorohydrin via a cyclic chloronium ion intermediate. When the chlorohydrin is treated with strong base, HCI is eliminated and the epoxide is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions ~A 1. Cl₂, H₂O 2. NaOH Ci: XII OH O H₂O :CI: llaarrow_forwardDraw the product that is expected when each of the following compound undergoes a ring-closing metathesis (RCM). Include stereochemistry in your answer.arrow_forward
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