Exam 29: Amino Acids and Proteins
Exam 1: Structure and Bonding70 Questions
Exam 2: Acids and Bases48 Questions
Exam 3: Introduction to Organic Molecules and Functional Groups48 Questions
Exam 4: Alkanes56 Questions
Exam 5: Stereochemistry68 Questions
Exam 6: Understanding Organic Reactions43 Questions
Exam 7: Alkyl Halides and Nucleophilic Substitution64 Questions
Exam 8: Alkyl Halides and Elimination Reactions45 Questions
Exam 9: Alcohols, Ethers and Epoxides49 Questions
Exam 10: Alkenes47 Questions
Exam 11: Alkynes45 Questions
Exam 12: Oxidation and Reduction43 Questions
Exam 13: Mass Spectrometry and Infrared Spectroscopy42 Questions
Exam 14: Nuclear Magnetic Resonance Spectroscopy43 Questions
Exam 15: Radical Reactions43 Questions
Exam 16: Conjugation, Resonance, and Dienes44 Questions
Exam 17: Benzene and Aromatic Compounds40 Questions
Exam 18: Electrophilic Aromatic Substitution51 Questions
Exam 19: Carboxylic Acids and the Acidity of the O-H Bond44 Questions
Exam 20: Introduction to Carbonyl Chemistry; Organometallic Reagents; Oxidation and Reduction53 Questions
Exam 21: Aldehydes and Ketones Nucleophilic Addition45 Questions
Exam 22: Carboxylic Acids and Derivatives47 Questions
Exam 23: Substitution Reactions of Carbonyl Compounds at the Alpha-Carbon41 Questions
Exam 24: Carbonyl Condensation Reactions45 Questions
Exam 25: Amines58 Questions
Exam 26: Carbon-Carbon Bond Forming Reactions in Organic Synthesis41 Questions
Exam 27: Pericyclic Reactions52 Questions
Exam 28: Carbohydrates41 Questions
Exam 29: Amino Acids and Proteins41 Questions
Exam 30: Lipids41 Questions
Exam 31: Synthetic Polymers41 Questions
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Why does the formation of salts of a racemic mixture of N-acetyl valine with a single enantiomer of -methylbenzylamine enable the separation of the two enantiomers of N-acetyl valine?
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(Multiple Choice)
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Correct Answer:
B
Below is a proposed method for resolving a racemic mixture of (R)- and (S)-phenylalanine. Upon separation of the products, will this method produce (R)- or (S)-phenylalanine? 
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(Multiple Choice)
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Correct Answer:
B
Which of the following amino acids is achiral?
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(Multiple Choice)
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Correct Answer:
B
Which of the following is the correct structure for aspartic acid at pH = 1? 
(Multiple Choice)
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What is the configuration of naturally occurring amino acids?
(Multiple Choice)
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What is the appropriate sequence of reaction conditions used to synthesize valine from acetamidomalonic ester? 
(Multiple Choice)
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Which of the following is the major advantage of the Merrifield synthesis of peptides?
(Multiple Choice)
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What is the IUPAC or common name for the following compound? 
(Multiple Choice)
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What are the basic steps in the Merrifield peptide synthesis?
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Below is a 2D chromatogram that shows the separation of five amino acids. In this technique, the amino acid mixture is first separated by chromatography using a polar solvent system. Then the plate is rotated 90°, and the amino acids are further separated by electrophoresis. Identify the spots obtained from a mixture of Trp, Glu, Lys, Ile and Thr. A table with isoelectric points is included to aid in solving this problem.
amino acid pI value
Trp
5)9
Glu
3)2
Lys
9)7
Ile
6)0
Thr
5)6
(Multiple Choice)
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What amino acid is at the N-terminus of the following peptide? 
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Which of the following correctly describes the tertiary structure of a peptide?
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Reaction of a polypeptide, composed of 12 amino acids, with carboxypeptidase A releases Met (C-terminal amino acid). The polypeptide undergoes partial hydrolysis to give 12 groups of peptides. Use the groups of overlapping amino acids to determine the proper sequence of this polypeptide. Note: Since these lists of peptides are separated by commas, they are not necessarily in the proper sequence.
1. Ser, Lys, Trp
2. Gly, His, Ala
3. Glu, Val, Ser
4. Leu, Glu, Ser
5. Met, Ala, Gly
6. Ser, Lys, Val
7. Glu, His
8. Leu, Lys, Trp
9. Lys, Ser
10. Glu, His, Val
11. Trp, Leu, Glu
12. Ala, Met
(Multiple Choice)
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