The amino acid glycine is often used as the main ingredient of a buffer in biochemical experiments. The amino group of glycine, which has a pK, of 9.6, can exist either in the protonated form -NH equilibrium or as the free base -NH₂, because of the reversible RÃNH →R-NH, + H* In what pH range can glycine be used as an effective buffer due to its amino group? How much 5 M KOH must be added to 1.0 L of 0.1 M glycine at pH 9.0 to bring its pH to 10.0? In a 0.1 M solution of glycine at pH 9.0, what fraction of glycine has its amino group in the-NH; form? When 99% of the glycine is in its -NH3 form, what is the numerical relation between the pH of the solution and the pK, of the amino group?

Chemistry & Chemical Reactivity
9th Edition
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Chapter16: Principles Of Chemical Reactivity: The Chemistry Of Acids And Bases
Section: Chapter Questions
Problem 116IL: Amino acids are an important group of compounds. At low pH, both the carboxylic acid group (CO2H)...
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The amino acid glycine is often used as the main ingredient of a buffer in biochemical experiments. The amino group of glycine,
which has a pk of 9.6, can exist either in the protonated form -NH or as the free base -NH₂, because of the reversible
equilibrium
R-NH² ⇒ R-NH₂ + H*
In what pH range can glycine be used as an effective
buffer due to its amino group?
How much 5 M KOH must be added to 1.0 L of 0.1 M
glycine at pH 9.0 to bring its pH to 10.0?
In a 0.1 M solution of glycine at pH 9.0, what fraction of
glycine has its amino group in the -NH; form?
When 99% of the glycine is in its -NH, form, what is
the numerical relation between the pH of the solution
and the pK, of the amino group?
A
Transcribed Image Text:The amino acid glycine is often used as the main ingredient of a buffer in biochemical experiments. The amino group of glycine, which has a pk of 9.6, can exist either in the protonated form -NH or as the free base -NH₂, because of the reversible equilibrium R-NH² ⇒ R-NH₂ + H* In what pH range can glycine be used as an effective buffer due to its amino group? How much 5 M KOH must be added to 1.0 L of 0.1 M glycine at pH 9.0 to bring its pH to 10.0? In a 0.1 M solution of glycine at pH 9.0, what fraction of glycine has its amino group in the -NH; form? When 99% of the glycine is in its -NH, form, what is the numerical relation between the pH of the solution and the pK, of the amino group? A
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