Chapter 29: Q14P (page 1152)
Question: Into how many peaks will each proton shown in green be split?
a.

b.

c.

d.

e.
Image Caption
f.

Short Answer
a. 3 and 4
b. 2 and 4
c. 1, 3, and 3
d. 2 and 2
e. 2 and 2
f. 2 and 3
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Chapter 29: Q14P (page 1152)
Question: Into how many peaks will each proton shown in green be split?
a.

b.

c.

d.

e.
Image Caption
f.

a. 3 and 4
b. 2 and 4
c. 1, 3, and 3
d. 2 and 2
e. 2 and 2
f. 2 and 3
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Name each peptide using both the one-letter and the three-letter abbreviations for the names of the component amino acids.
a.

b.

Name each peptide using both the three-letter and one-letter abbreviations of the component amino acids.

What aldehyde is needed to synthesize each amino acid by the Strecker synthesis?
(a) Valine;
(b) Leucine;
(c) Phenylalanine.
An octapeptide contains the following amino acids: Arg, Glu, His, Ile, Leu, Phe, Tyr, and Val. Carboxypeptidase treatment of the octapeptide forms Phe and a heptapeptide. Treatment of the octapeptide with chymotrypsin forms two tetrapeptides, A and B. Treatment of A with trypsin yields two dipeptides, C and D. Edman degradation cleaves the following amino acids from each peptide: Glu (octapeptide), Glu (A), Ile (B), Glue (C), and Val (D). Partial hydrolysis of tetrapeptide B forms Ile-Leu in addition to other products. Deduce the structure of the octapeptide and fragments A-D.
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?
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