Step 4: You have determined that one of the precursors is a vinyl halide, while the other is a vinyl boronate. Deduce the- structures of the precursors if the halide is a bromine and the boronate is a boronic acid (-B(OH,)). Clearly show stereochemistry of each alkene.

Step 4: You have determined that one of the precursors is a vinyl halide, while the other is a vinyl boronate. Deduce the- structures of the precursors if the halide is a bromine and the boronate is a boronic acid (-B(OH,)). Clearly show stereochemistry of each alkene.

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

100%

Synthesize the compound shown using a Suzuki coupling. Deduce the structures of the starting materials.
Step 4: You have determined that one of the precursors is a vinyl halide, while the other is a vinyl boronate. Deduce the
structures of the precursors if the halide is a bromine and the boronate is a boronic acid (-B(OH,)). Clearly show
stereochemistry of each alkene.
Draw the two starting materials.
Select
Draw
Rings
More
Erase
Br
FEB
3.
étv N li 1
W
MacBoolk Air

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