a. Look at the non-natural amino acid below and note that the pka's of particular groups are provided. Determine the Isoelectric point of this amino acid (p). Please answer as a letter choice only (i.e, "E" not "E)" pka - 4.20 HO. pKa = 2.00 HO. NH, pka - 9.50 A) pl = 6.20 C) pl = 5.23 B) pl = 3.10 D) pl = 5.75 b. Which drawing best indicates the form of the amino acid at a pH of 8.4? pka4.20 pka2.00 NH, pka950 HO. NH, NH, c. Which of the following dipeptides is leucinyiserine? HN. но D. OH он OH HO

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Chapter1: Chemical Foundations
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Question one parts A though H
d. You have a plan to make the cellular signaling peptide RGD (Arg-Gly-Asp). If you are beginning from
the Arginine (Arg) amino acid, which amino acid(s) will require NH2 protection to optimize the
a. Look at the non-natural amino acid below and note that the pka's of particular groups are provided.
synthesis?
Determine the Isoelectric point of this amino acid (pl). Please answer as a letter choice only (i.e., "E"
not "E)"
A) All 3 amino acids will need NH2 protection
B) Gly and Asp will need NH2 protection
C) Arg and Gly will need NH2 protection
pka = 4.20 HO
но
Ка 2.00
HO,
D) Only Arg
NH,
pКа 9.50
E. Which of the following amino acids will not produce a purple color (indicative of 2 ninhydrin
molecules binding) when reacted with ninhydrin?
A) pl = 6.20
B) pl = 3.10
A) phenylalanine
C) pl = 5.23
D) pl = 5.75
B) valine
C) proline
b. Which drawing best indicates the form of the amino acid at a pH of 8.4?
D) histidine
F. If you had a mixture of leucine, arginine, and glutamic acid in a pH of 6 and applied a drop onto paper
connected to an electrophoresis apparatus. Which of these would move toward the cathode (-).
pka -2.00
HO.
pka = 4.20
HO
A) Leucine
NH,
pka -9.50
B) Arginine
C) Glutamic Acid
A.
В.
D) None of them
но,
OH
HO.
G. True/False - Dicyclohexylcarbodiimide is a typical reagent in peptide synthesis for protecting
NH,
NH,
carboxylic acid groups.
C.
D.
H. True/False t-butoxycarbonyl dicarbonate (Boc20) adds a t-butoxy carbonyl group to the amine
но
.
NH,
NH3
portion of the amino acid creating an amide (carbamate) and protects the amine portion from side
reactions.
c. Which of the following dipeptides is leucinylserine?
A.
B.
OH
H,N.
OH
H,N.
OH
но
D.
C.
OH
HN.
OH
HN.
он
но
Transcribed Image Text:Question one parts A though H d. You have a plan to make the cellular signaling peptide RGD (Arg-Gly-Asp). If you are beginning from the Arginine (Arg) amino acid, which amino acid(s) will require NH2 protection to optimize the a. Look at the non-natural amino acid below and note that the pka's of particular groups are provided. synthesis? Determine the Isoelectric point of this amino acid (pl). Please answer as a letter choice only (i.e., "E" not "E)" A) All 3 amino acids will need NH2 protection B) Gly and Asp will need NH2 protection C) Arg and Gly will need NH2 protection pka = 4.20 HO но Ка 2.00 HO, D) Only Arg NH, pКа 9.50 E. Which of the following amino acids will not produce a purple color (indicative of 2 ninhydrin molecules binding) when reacted with ninhydrin? A) pl = 6.20 B) pl = 3.10 A) phenylalanine C) pl = 5.23 D) pl = 5.75 B) valine C) proline b. Which drawing best indicates the form of the amino acid at a pH of 8.4? D) histidine F. If you had a mixture of leucine, arginine, and glutamic acid in a pH of 6 and applied a drop onto paper connected to an electrophoresis apparatus. Which of these would move toward the cathode (-). pka -2.00 HO. pka = 4.20 HO A) Leucine NH, pka -9.50 B) Arginine C) Glutamic Acid A. В. D) None of them но, OH HO. G. True/False - Dicyclohexylcarbodiimide is a typical reagent in peptide synthesis for protecting NH, NH, carboxylic acid groups. C. D. H. True/False t-butoxycarbonyl dicarbonate (Boc20) adds a t-butoxy carbonyl group to the amine но . NH, NH3 portion of the amino acid creating an amide (carbamate) and protects the amine portion from side reactions. c. Which of the following dipeptides is leucinylserine? A. B. OH H,N. OH H,N. OH но D. C. OH HN. OH HN. он но
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