Chapter 29: Q10P (page 1162)
Which of the following amines can be used to resolve a racemic mixture of amino acids?
(a)
(b)
(c)
(d)
Short Answer
Answer
(c)
(d)
Chapter 29: Q10P (page 1162)
Which of the following amines can be used to resolve a racemic mixture of amino acids?
(a)
(b)
(c)
(d)
Answer
(c)
(d)
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Get started for freeDevise a synthesis of the following dipeptide from amino acid starting materials.
Explain why the pKaof the -NH3+group of an -amino acid is lower than the pKaof the ammonium ion derived from a amine . For example, pKaof the group of alanine is 9.87 but the pKaof is 10.63.
For the tetra peptide Asp–Arg–Val–Tyr:
a. Name the peptide using one-letter abbreviations.
b. Draw the structure.
c. Label all amide bonds.
d. Label the N-terminal and C-terminal amino acids
Draw the other three stereoisomers of L-isoleucine, and label the stereogenic centers as R or S.
a. Draw the structure of the tripeptide A-A-A, and label the two ionizable functional groups.
b. What is the predominant form of A-A-A at pH=1?
c. The values for the two ionizable functional groups (3.39 and 8.03) differ considerably from the values of alanine (2.35 and 9.87;see table 29.1). Account for the observed differences.
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