HBr 1.2 & 1.4-addition H₂SO4 180°C (a) products from ether cleavage (1) Na (2) C₂H5-Br (b) OH 2 HI (c) (d) alkene formation (E2) Williamson ether formation (SN2) CN. MCPBA CH₂Cl2 (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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35.) 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?
HBr
1.2 &1.4-addition
H₂SO4
180°C
(a)
CN.
products from ether cleavage
(1) Na
(2) C₂H5-Br
(b)
(c)
(d)
alkene formation (E2)
Williamson ether formation (SN2)
MCPBA
CH₂Cl2
(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).
OH
2 HI
Transcribed Image Text:HBr 1.2 &1.4-addition H₂SO4 180°C (a) CN. products from ether cleavage (1) Na (2) C₂H5-Br (b) (c) (d) alkene formation (E2) Williamson ether formation (SN2) MCPBA CH₂Cl2 (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). OH 2 HI
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