Why is the pKa value of protonated hydroxylamine (6.0) so much lower than the pKa value of a protonated primary amine such as protonated methylamine (10.7)?
Why is the pKa value of protonated hydroxylamine (6.0) so much lower than the pKa value of a protonated primary amine such as protonated methylamine (10.7)?
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
Chapter27: Amino Acids And Proteins
Section: Chapter Questions
Problem 27.33P
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Why is the pKa value of protonated hydroxylamine (6.0) so much lower than the pKa value of a protonated primary
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