Sodium Borohydride Reduction of a Suzuki Cross-Coupled Product Suzuki Cross-Coupling Reactions: Synthesis of an Unsymmetrical Biaryl via Suzuki Coupling Reaction? Purpose: Perform the sodium borohydride reduction of the carbonyl group of the intermediate biaryl product, and determine the biaryl structure from its melting point. R. R. OH NaBH4 CH3OH H2O R' R' R = H, CH3 R' = H, CH3, OCH3
Sodium Borohydride Reduction of a Suzuki Cross-Coupled Product Suzuki Cross-Coupling Reactions: Synthesis of an Unsymmetrical Biaryl via Suzuki Coupling Reaction? Purpose: Perform the sodium borohydride reduction of the carbonyl group of the intermediate biaryl product, and determine the biaryl structure from its melting point. R. R. OH NaBH4 CH3OH H2O R' R' R = H, CH3 R' = H, CH3, OCH3
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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In the Sodium Borohydride Reduction of a Suzuki Cross-Coupled Product,
If 4-(4-methylphenyl)benzaldehyde is the reagent in this reaction, what is the name and structure of the product of this reaction.

Transcribed Image Text:Sodium Borohydride Reduction of a Suzuki Cross-Coupled Product
Suzuki Cross-Coupling Reactions: Synthesis of an Unsymmetrical Biaryl via Suzuki
Coupling Reaction?
Purpose: Perform the sodium borohydride reduction of the carbonyl group of the
intermediate biaryl product, and determine the biaryl structure from its melting
point.
R.
R.
OH
NaBH4
CH3OH
H2O
R'
R'
R = H, CH3
R' = H, CH3, OCH3

Transcribed Image Text:R
Na BHy
CH3 OH
HzO
CH3
4-(4 methylphenyl-) benzaldehyde
R'
R:H,CH3
R=H, CAg, OCH3
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