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ăzidé âñd á third pathway using Gabriel synthesis) b. Starting reagent: 2-phenlethanal (Show two synthesis pathways. One pathway involving sodium cyanoborohydride and a second pathway involving an oxime.)

ăzidé âñd á third pathway using Gabriel synthesis) b. Starting reagent: 2-phenlethanal (Show two synthesis pathways. One pathway involving sodium cyanoborohydride and a second pathway involving an oxime.)

Chemistry
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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Please provide the solution to part b (image attached)

Show how you would synthesize 2-phenylethanamine (PhCH2CH2NH2) starting from the following reagents. a. Starting reagent: PHCH2CH2B (Show three synthesis pathways: One pathway with NH3, explaining what is important to make the reaction work, a second pathway involving an azide and a third pathway using Gabriel synthesis) b. Starting reagent: 2-phenlethanal (Show two synthesis pathways. One pathway involving sodium cyanoborohydride and a second pathway involving an oxime.)
Transcribed Image Text:Show how you would synthesize 2-phenylethanamine (PhCH2CH2NH2) starting from the following reagents. a. Starting reagent: PHCH2CH2B (Show three synthesis pathways: One pathway with NH3, explaining what is important to make the reaction work, a second pathway involving an azide and a third pathway using Gabriel synthesis) b. Starting reagent: 2-phenlethanal (Show two synthesis pathways. One pathway involving sodium cyanoborohydride and a second pathway involving an oxime.)
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