12 & 1.4-addition products from ether cleav Br HBr 2 HI Br Cl,2) (c) (d) OH (1) Na H2SO4 (2) C2H5-Br (b) 180°C (a) Williamson ether formation (SN2) alkene formation (E2)
12 & 1.4-addition products from ether cleav Br HBr 2 HI Br Cl,2) (c) (d) OH (1) Na H2SO4 (2) C2H5-Br (b) 180°C (a) Williamson ether formation (SN2) alkene formation (E2)
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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Help understanding the mechanism for reactions c and b please

Transcribed Image Text:25) What would be the preferred product for each of the following reactions (hint: ether formation,
ether-cleavage, diene formation, 1,2/1,4-addition, epoxidation and Diels-Alder cycloaddition)2
1.2 & 1.4-addition
products from ether cleav
HBr
2 HI
(c)
(d)
Cl,2)
OH
H2SO4
(1) Na
180°C
(2) C2H5-Br
(b)
(a)
alkene formation (E2)
Williamson ether formation (SN2)
CN.
МСРВА
CH2CI2
(e)
(f)
epoxidation
Diels-Alder Rxn
Show the mechanism for the formation of 1.2- and 1,4-addition products (c) from conjugated
diene, and the Williamson ether synthesis (b).
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