Chapter 29: Q10. (page 1162)
Which of the following amines can be used to resolve a racemic mixture of amino acids?
(a)
(b)
(c)
(d)
Short Answer
(c)
(d)
Chapter 29: Q10. (page 1162)
Which of the following amines can be used to resolve a racemic mixture of amino acids?
(a)
(b)
(c)
(d)
(c)
(d)
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Get started for freeWrite out the steps for the synthesis of each peptide using the Merrifield method:
What form exists at the isoelectric point of each of the following amino acids: (a) valine; (b)leucine; (c)proline; (d) glutamic acid.
Draw the structure of leu-enkephalin, a pentapeptide that acts as an analgesic and opiate, and has the following sequence: Tyr–Gly–Gly–Phe–Leu. (The structure of a related peptide, met-enkephalin,
appeared in Section 22.6B.)
a.(S)-Penicillamine, an amino acid that does not occur in proteins, is used as a copper chelating agent to treat Wilson’s disease, an inherited defect in copper metabolism.
(R)-Penicillamine is toxic, sometimes causing blindness. Draw the structures of (R) and (S)-penicillamine.
b. What disulfide is formed from oxidation of L-penicillamine?
Tryptophan is not classified as a basic amino acid even though it has a heterocycle containing a nitrogen atom. Why is the N atom in the five-membered ring of tryptophan not readily protonated by acid?
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