Propose a synthesis for the transformations shown below (no mechanisms needed, just products/intermediates and reagents). You will get full credit if you figure out two out of three. Clearly indicate which two you want us to grade. 4. Propose a synthesis for the transformations shown below (no mechanisms needed, justproducts/intermediates and reagents). You will get full credit if you figure out two out ofthree. Clearly indicate which two you want us to grade.Synthesis 1:Synthesis 2:Synthesis 3:??Br Br?HO

Step 1: Synthesis 1:3-methylbut-1-yne with sodamide gives acetylide anion, which on reaction with…

4. Propose a synthesis for the transformations shown below (no mechanisms needed, just products/intermediates and reagents). You will get full credit if you figure out two out of three. Clearly indicate which two you want us to grade. Synthesis 1: Synthesis 2: Synthesis 3: ? ? Br Br ? H O

4. Propose a synthesis for the transformations shown below (no mechanisms needed, just products/intermediates and reagents). You will get full credit if you figure out two out of three. Clearly indicate which two you want us to grade. Synthesis 1: Synthesis 2: Synthesis 3: ? ? Br Br ? H O

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter8: Haloalkanes, Halogenation, And Radical Reactions

Section: Chapter Questions

Problem 8.28P

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Question

Propose a synthesis for the transformations shown below (no mechanisms needed, just products/intermediates and reagents). You will get full credit if you figure out two out of three. Clearly indicate which two you want us to grade.

4. Propose a synthesis for the transformations shown below (no mechanisms needed, just
products/intermediates and reagents). You will get full credit if you figure out two out of
three. Clearly indicate which two you want us to grade.
Synthesis 1:
Synthesis 2:
Synthesis 3:
?
?
Br Br
?
H
O

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