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What is the separation of a racemic mixture into its component enantiomers called?


A) diastereomers
B) meso
C) resolution
D) neutralization

E) A) and D)
F) None of the above

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Give the order (1st to last) in which the following amino acids would be eluted with a buffer of pH = 4 from a column containing a cationic-exchange resin (Dowex 50) : Arg (pI = 10.8) , Ser (pI = 5.7) , Asp (pI = 2.8) and His (pI = 7.6) .


A) His, Ser, Asp, Arg
B) Arg, His, Ser, Asp
C) His, Ser, Arg, Asp
D) Asp, Ser, His, Arg

E) C) and D)
F) A) and B)

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Which of the following is the correct structure for alanine at pH = 7? Which of the following is the correct structure for alanine at pH = 7?   A)  A B)  B C)  C D)  D


A) A
B) B
C) C
D) D

E) B) and C)
F) C) and D)

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What are the only non-covalent bonds that stabilize the tertiary structure of a peptide?


A) hydrogen bonds
B) disulfide bonds
C) Van der Waal bonds
D) ionic bonds

E) B) and C)
F) B) and D)

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Which of the following aldehydes would be a good starting material in the Strecker synthesis of phenylalanine? Which of the following aldehydes would be a good starting material in the Strecker synthesis of phenylalanine?   A)  A B)  B C)  C D)  D


A) A
B) B
C) C
D) D

E) B) and C)
F) A) and B)

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Which is the correct structure for the amino acid cysteine? Which is the correct structure for the amino acid cysteine?   A)  A B)  B C)  C D)  D


A) A
B) B
C) C
D) D

E) A) and B)
F) A) and C)

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What reagents would you use to convert acetaldehyde into alanine?


A) NH3
B) HCN
C) NaCN, NH4Cl
D) NaNH2

E) A) and B)
F) A) and C)

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Which is the correct structure for the amino acid proline? Which is the correct structure for the amino acid proline?   A)  A B)  B C)  C D)  D


A) A
B) B
C) C
D) D

E) B) and D)
F) A) and B)

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Amino acid synthesis is possible by all except one of the pathways listed. Which is not a synthetic pathway for amino acids?


A) Amination of malonic ester followed by hydrolysis and decarboxylation.
B) Nucleophilic addition of NH3 to an aldehyde followed by addition of cyanide to the imine, and, finally, hydrolysis.
C) SN2 reaction using an -halo carboxylic acid with ammonia as the nucleophile.
D) Reaction of NH4Cl and NaCN with an aldehyde followed by an acidic work-up.

E) All of the above
F) A) and D)

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Which of the following is the structure of the amino acid lysine? Which of the following is the structure of the amino acid lysine?   A)  A B)  B C)  C D)  D


A) A
B) B
C) C
D) D

E) A) and B)
F) A) and C)

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Which of the following correctly describes the Merrifield synthesis?


A) It uses a solid phase technique for the synthesis of peptides.
B) It uses DCC (dicyclohexylcarbodiimide) to form the amide bond in a peptide synthesis.
C) It uses BOC (tert-butoxycarbonyl) as a protecting group for peptide synthesis.
D) It uses aqueous phase techniques for the synthesis of large polypeptides.

E) C) and D)
F) A) and B)

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What is the name given to the pH at which the concentration of the zwitterionic form of an amino acid is at a maximum concentration?


A) electric point
B) dipolar point
C) neutral point
D) isoelectric point

E) C) and D)
F) B) and C)

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Which is the correct structure for serine? Which is the correct structure for serine?   A)  A B)  B C)  C D)  D


A) A
B) B
C) C
D) D

E) All of the above
F) B) and C)

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What is the major organic product for the following reaction? What is the major organic product for the following reaction?   A)  A B)  B C)  C D)  D


A) A
B) B
C) C
D) D

E) A) and B)
F) B) and D)

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Why do amide bonds exist as reasonably stable s-cis or s-trans isomers at room temperature?


A) These amide bonds are not stable.
B) There is partial double bond character between the carbonyl carbon and the nitrogen atom.
C) The oxygen atom is hydrogen-bonded with the nitrogen atom.
D) The side-chains can form hydrogen bonds.

E) All of the above
F) A) and D)

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Which of the following compounds is not an amino acid? Which of the following compounds is not an amino acid?   A)  A B)  B C)  C D)  D


A) A
B) B
C) C
D) D

E) B) and C)
F) All of the above

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Which of the following amino acids does not have an L-isomer?


A) alanine
B) valine
C) glycine
D) leucine

E) A) and B)
F) None of the above

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What amino acid is at the C-terminus of the following peptide? What amino acid is at the C-terminus of the following peptide?   A)  valine B)  serine C)  alanine D)  proline


A) valine
B) serine
C) alanine
D) proline

E) B) and C)
F) A) and B)

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What is formed by the combination of four amino acids?


A) a protein
B) a polypeptide
C) a tripeptide
D) a tetrapeptide

E) All of the above
F) A) and B)

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Which one of the following naturally occurring amino acids does not have an S configuration?


A) cysteine
B) alanine
C) tyrosine
D) isoleucine

E) None of the above
F) A) and B)

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