:0: :NH2 NH3 NH4* CN- hydrolysis R H. R `CN R CO" 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 reaction arrows to show the movement of electrons. Arrow-pushing Instructions H-A :ö: :ÖH R H. :B A HB R

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Chapter1: Chemical Foundations
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:0:
:NH2
hydrolysis
NH3
NH4* CN-
R
H.
R
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 reaction arrows to show the movement of electrons.
Arrow-pushing Instructions
H-A
:0:
:ÖH
R
A HB
:B
R
Transcribed Image Text::0: :NH2 hydrolysis NH3 NH4* CN- R H. R 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 reaction arrows to show the movement of electrons. Arrow-pushing Instructions H-A :0: :ÖH R A HB :B R
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