A) Electric point
B) Dipolar point
C) Neutral point
D) Isoelectric point
Correct Answer
verified
Multiple Choice
A) Diastereomers
B) Meso
C) Resolution
D) Neutralization
Correct Answer
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Multiple Choice
A) They form amides.
B) They form diastereomers.
C) They form salts.
D) They form meso compounds.
Correct Answer
verified
Multiple Choice
A) A
B) B
C) C
D) D
Correct Answer
verified
Multiple Choice
A) A protein
B) A polypeptide
C) A tripeptide
D) A tetrapeptide
Correct Answer
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Multiple Choice
A) A
B) B
C) C
D) D
Correct Answer
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Multiple Choice
A) NH3
B) HCN
C) NaCN, NH4Cl
D) NaNH2
Correct Answer
verified
Multiple Choice
A) A
B) B
C) C
D) D
Correct Answer
verified
Multiple Choice
A) A
B) B
C) C
D) D
Correct Answer
verified
Multiple Choice
A) D
B) S
C) L
D) R
Correct Answer
verified
Multiple Choice
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
Correct Answer
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Multiple Choice
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.
Correct Answer
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Multiple Choice
A) A
B) B
C) C
D) D
Correct Answer
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Multiple Choice
A) Alanine
B) Valine
C) Glycine
D) Leucine
Correct Answer
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Multiple Choice
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
Correct Answer
verified
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