The above synthesis was designed using the Organic Chemistry Roadmaps in the appendix of your textbook. In this synthesis, reagents from the table (shown in blue) are used to carry out the indicated reactions. In the box below, draw the structure of compound b .

The above synthesis was designed using the Organic Chemistry Roadmaps in the appendix of your textbook. In this synthesis, reagents from the table (shown in blue) are used to carry out the indicated reactions. In the box below, draw the structure of compound b .

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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Question

Reagents
m. 2 equivalents of NaNH2
H2, Lindlar's catalyst
Na / NH3
p. H2SO4, HgSO4
q. (sia)2BH then H2O2, NaOH
1 equivalent of NaNH2
a. HCI
b. HBr
n.
c. H20, H2SO4
d. Br2
0.
n
Cl2
е.
H2, Pd
g. Br2, H20
h. Cl2, H2O
f.
r.
compound a
Os04 then NaHSO3
j. Hg(OAc)2, H20 then NABH4
k. BH3 then H2O2, NaOH
Oz then (CH3)2S
i.
compound b
I.
The above synthesis was designed using the Organic Chemistry Roadmaps in the appendix of your textbook.
In this synthesis, reagents from the table (shown in blue) are used to carry out the indicated reactions. In the box below, draw the structure of compound b.
• Use the wedge/hash bond tools to indicate stereochemistry where it exists.
• Consider E/Z stereochemistry of alkenes.
• If more than one structure fits the description, draw them all.
• If a compound is formed more than once, add another sketcher and draw it again.
• If the reaction produces a racemic mixture, draw both stereoisomers.
Separate structures with + signs from the drop-down menu.

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