A transamination can be summarized as an amino group (-NH3) of an amino acid and the keto group (C-0) of an a-keto acid changing places and forming different amino acid and a-keto acid products, as in the generic reaction below: amino acid 1 + a-keto acid 1 a-keto acid 2 + amino acid 2 Draw the a-keto acid product of the transamination of an a-keto acid with an amino acid that has the side chain X RC-COO H3N-CH-C-O Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Show formal charges on all atoms. > View Available Hint(s)
A transamination can be summarized as an amino group (-NH3) of an amino acid and the keto group (C-0) of an a-keto acid changing places and forming different amino acid and a-keto acid products, as in the generic reaction below: amino acid 1 + a-keto acid 1 a-keto acid 2 + amino acid 2 Draw the a-keto acid product of the transamination of an a-keto acid with an amino acid that has the side chain X RC-COO H3N-CH-C-O Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Show formal charges on all atoms. > View Available Hint(s)
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
Chapter16: Aldehydes And Ketones
Section16.8: Addition Of Nitrogen Nucleophiles
Problem CQ: The given mechanism of transamination reaction is shown below, What is the role of the pyridinium...
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