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 pKa of
9.6, can exist either in the protonated form (ONH3 ) or as
the free base (ONH2), because of the reversible equilibrium
R-NH(3)+ ------>R-NH(2) + H+
(a) In what pH range can glycine be used as an effective
buffer due to its amino group?
(b) In a 0.1 M solution of glycine at pH 9.0, what fraction
of glycine has its amino group in the ONH3 form?
(c) 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 exactly 10.0?
(d) When 99% of the glycine is in its ONH3 form, what
is the numerical relation between the pH of the solution and
the pKa of the amino group?
How do i even start with this problem? Any hints appreciated.
2007-06-07
09:24:19
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3 answers
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asked by
untamedblade
1
in
Science & Mathematics
➔ Chemistry