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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) B) and C)
F) None of the above

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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 C)
F) All of the above

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Why does the formation of salts of a racemic mixture of N-acetyl valine with a single enantiomer of a-methylbenzylamine enable the separation of the two enantiomers of N-acetyl valine?


A) They form amides.
B) They form diastereomers.
C) They form salts.
D) They form meso compounds.

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

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

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

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

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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 C)
F) A) and B)

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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 D)
F) B) and C)

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

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What is the configuration of naturally occurring amino acids?


A) D
B) S
C) L
D) R

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

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Which of the following correctly describes the tertiary structure of a peptide?


A) the three-dimensional conformations of localized regions of a protein
B) the particular sequence of amino acids that are joined together by peptide bonds
C) the structure is defined by the b-pleated sheet form
D) the three-dimensional shape adopted by the entire peptide

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

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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) A) and B)
F) None 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 C)
F) A) and D)

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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 a-halo carboxylic acid with ammonia as the nucleophile
D) Reaction of NH4Cl and NaCN with an aldehyde followed by an acidic work-up

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

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