:NH2 NH3 NH, CN hydrolysis CN R coo e-amino acids can be prepared by the Strecker zpathesis, a two-step process in which an aldehyde is trested with ammonium cyanide, followed by hydrolysis of the amino nitrile intermediate with aqueous acid. Propose a mechanism for the illustrated step of the reaction by drawing reaction arrows to show the movement of electrons. Arrow-pushing Instructions NH2 NH2 :CN R H. R "CN

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter29: The Organic Chemistry Of Metabolic Pathways
Section29.SE: Something Extra
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NH, CN"
:NH2
NH3
hydrolysis
H.
CN
R
a-amino acids can be prepared by the Strecker synthesis, a two-step process in which an aldehyde is treated with ammonium cyanide, followed by hydrolysis of the amino nitrile intermediate
with aqueous acid. Propose a mechanism for the illustrated step of the reaction by drawing rezction arrows to show the movement of electrons.
Arrow-pushing Instructions
NH2
NH2
:CN
R
R
CN
Transcribed Image Text::0: NH, CN" :NH2 NH3 hydrolysis H. CN R a-amino acids can be prepared by the Strecker synthesis, a two-step process in which an aldehyde is treated with ammonium cyanide, followed by hydrolysis of the amino nitrile intermediate with aqueous acid. Propose a mechanism for the illustrated step of the reaction by drawing rezction arrows to show the movement of electrons. Arrow-pushing Instructions NH2 NH2 :CN R R CN
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