Chapter 21: Q4P (page 993)
Do any other amino acids in Table 21.2 have more than one asymmetric center?
Short Answer
Isoleucine is the only other amino acid that has more than one asymmetric center.
Chapter 21: Q4P (page 993)
Do any other amino acids in Table 21.2 have more than one asymmetric center?
Isoleucine is the only other amino acid that has more than one asymmetric center.
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What amino acid is formed using the N-phthalimidomalonic ester synthesis when the following alkyl halides are used in the third step?
(a)

(b)
A professor was preparing a manuscript for publication in which she reported that the pI of the tripeptide Lys-Lys-Lys was 10.6. One of her studentspointed out that there must be an error in her calculations because the pKa of the e-amino group of lysine is 10.8 and the pI of the tripeptide has to begreater than any of its individual pKa values. Was the student correct?
Esterase is an enzyme that catalyzes the hydrolysis of esters. It hydrolyzes esters of L-amino acids more rapidly than esters of D-amino acids. How can this enzyme be used to separate a racemic mixture of amino acids?
Why are buffer solutions of increasingly higher pH used to elute the column that generates the chromatogram shown in Figure 21.5? (Elutemeans wash out with a solvent.)
a. How many different octapeptides can be made from the 20 naturally occurring amino acids?
b. How many different proteins containing 100 amino acids can be made from the 20 naturally occurring amino acids?
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