:0: :NH2 NH3 NH, CN" hydrolysis 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 nitril 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 + H. :B A HB R

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Draw the arrow on top of the attached picture, do not attempt to draw it on your own, it needs to be seen clearly

:0:
:NH2
hydrolysis
NH3
NH,* CN"
`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
H.
:B
A
НВ
R
--
Transcribed Image Text::0: :NH2 hydrolysis NH3 NH,* CN" `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 H. :B A НВ R --
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