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Titrations of Amino Acids with Non-Ionizable R-Groups quiz
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What are the two ionizable groups present in amino acids with non-ionizable R groups?
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What are the two ionizable groups present in amino acids with non-ionizable R groups?
The two ionizable groups are the alpha amino group and the alpha carboxyl group.
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Terms in this set (15)
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What are the two ionizable groups present in amino acids with non-ionizable R groups?
The two ionizable groups are the alpha amino group and the alpha carboxyl group.
How many pKa values do amino acids with non-ionizable R groups have, and what do they correspond to?
They have two pKa values: one for the alpha amino group and one for the alpha carboxyl group.
What does the inflection point (midpoint) on a titration curve represent?
The inflection point represents the pKa value, where half of the acid has been neutralized.
What is the equivalence point on a titration curve?
The equivalence point is where 100% of an acid has been neutralized.
How is the isoelectric point (pI) of an amino acid with a non-ionizable R group calculated?
The pI is the average of the two pKa values of the amino and carboxyl groups.
At what point on the titration curve does the amino acid have a net charge of zero?
At the isoelectric point (pI), the amino acid has a net charge of zero.
What is the predominant structure of alanine at low pH (below both pKa values)?
Both the amino and carboxyl groups are protonated, giving alanine a net charge of +1.
What is the net charge of alanine at a pH equal to the pKa of the carboxyl group?
The net charge is +0.5 because the amino group is fully protonated (+1) and the carboxyl group is half deprotonated (-0.5).
What is the predominant structure of alanine at a pH between the two pKa values (near the pI)?
The amino group is protonated (NH3+) and the carboxyl group is deprotonated (COO-), resulting in a net charge of 0.
What is the net charge of alanine at a pH equal to the pKa of the amino group?
The net charge is -0.5 because the carboxyl group is fully deprotonated (-1) and the amino group is half protonated (+0.5).
What is the predominant structure of alanine at high pH (above both pKa values)?
Both the amino and carboxyl groups are deprotonated, giving alanine a net charge of -1.
What is the effective buffering range for each ionizable group in an amino acid?
The effective buffering range is within plus or minus one pH unit of each pKa value.
How many inflection points and equivalence points are present in the titration curve of an amino acid with a non-ionizable R group?
There are two inflection points and two equivalence points, one for each ionizable group.
What happens to the net charge of an amino acid as the pH increases across the titration curve?
The net charge becomes more negative as the pH increases.
What is the isoelectric point (pI) of alanine if its pKa values are 2.4 and 9.7?
The pI is (2.4 + 9.7) / 2 = 6.05.