Please provide the solution to part b (image attached) Show how you would synthesize 2-phenylethanamine (PhCH2CH2NH2) starting from thefollowing 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 anazide and a third pathway using Gabriel synthesis)b. Starting reagent: 2-phenlethanal (Show two synthesis pathways. One pathwayinvolving sodium cyanoborohydride and a second pathway involving an oxime.)

The question is based on the concept of organic reactions. We have to convert the reactant into…

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.)

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

Chapter19: Enolate Anions And Enamines

Section: Chapter Questions

Problem 19.57P

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Question

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.)

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