Chapter 21: Q10P (page 996)
Calculate the pI of each of the following amino acids:
a.asparagine b. arginine c. serine d. aspartate
Short Answer
(a) pI = 5.43
(b) pI = 10.76
(c) pI = 5.68
(d) pI = 2.98
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Chapter 21: Q10P (page 996)
Calculate the pI of each of the following amino acids:
a.asparagine b. arginine c. serine d. aspartate
(a) pI = 5.43
(b) pI = 10.76
(c) pI = 5.68
(d) pI = 2.98
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alpha- Amino acids can be prepared by treating an aldehyde with ammonia/trace acid, followed by hydrogen cyanide, followed by acid-catalyzed hydrolysis.
a. Draw the structures of the two intermediates formed in this reaction.
b. What amino acid is formed when the aldehyde that is used is 3-methylbutanal?
c. What aldehyde is needed to prepare isoleucine?
What dipeptides would be formed by heating a mixture of valine and N- protected leucine?
Alanine has pKa values of 2.34 and 9.69. Therefore, alanine exists predominately as a zwitterion in an aqueous solution with pH > ____ and pH < ____.
a. Which isomer—(R)-alanine or (S)-alanine—is d-alanine?
b. Which isomer—(R)-aspartate or (S)-aspartate—is d-aspartate?
c. Can a general statement be made relating R and S to d and l?
Explain the order of elution (with a buffer of pH 4) of the following pairs of amino acids through a column packed with Dowex 50 (Figure 21.3):
a. aspartate before serine c. valine before leucine
b. serine before alanine d. tyrosine before phenylalanine
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