Exam 19: Biomolecules: Amino Acids,peptides,and Proteins
Exam 1: Structure and Bonding30 Questions
Exam 2: Polar Covalent Bonds: Acids and Bases35 Questions
Exam 3: Organic Compounds: Alkanes and Their Stereochemistry32 Questions
Exam 4: Organic Compounds: Cycloalkanes and Their Stereochemistry18 Questions
Exam 5: Stereochemistry at Tetrahedral Centers33 Questions
Exam 6: An Overview of Organic Reactions32 Questions
Exam 7: Alkenes and Alkynes34 Questions
Exam 8: Reactions of Alkenes and Alkynes37 Questions
Exam 9: Aromatic Compounds36 Questions
Exam 10: Structure Determination: Mass Spectrometry,infrared Spectroscopy,and Ultraviolet Spectroscopy41 Questions
Exam 11: Structure Determination: Nuclear Magnetic Resonance Spectroscopy37 Questions
Exam 12: Organohalides: Nucleophilic Substitutions and Eliminations37 Questions
Exam 13: Alcohols,phenols,and Thiols: Ethers and Sulfides19 Questions
Exam 14: Aldehydes and Ketones: Nucleophilic Addition Reactions30 Questions
Exam 15: Carboxylic Acids and Nitriles23 Questions
Exam 16: Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions42 Questions
Exam 17: Carbonyl Alpha-Substitution and Condensation Reactions84 Questions
Exam 18: Amines and Heterocycles28 Questions
Exam 19: Biomolecules: Amino Acids,peptides,and Proteins36 Questions
Exam 20: Amino Acid Metabolism34 Questions
Exam 21: Biomolecules: Carbohydrates42 Questions
Exam 22: Carbohydrate Metabolism41 Questions
Exam 23: Biomolecules: Lipids and Their Metabolism31 Questions
Exam 24: Biomolecules: Nucleic Acids and Their Metabolism23 Questions
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Consider the following structure.Based on this structure answer the following question(s).
-Refer to instructions.Identify the C-terminal amino acid and the N-terminal amino acid.
(Essay)
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Write the equation for the reaction,using methanol (CH3OH),that would render the carboxyl group of alanine unreactive.
(Essay)
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Which of the following amino acids has an aromatic side chain?
(Multiple Choice)
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Which of the following tripeptides is not hydrolysed by chymotrypsin?
(Multiple Choice)
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Which of the following reagents can be used to cleave a tert-butoxycarbonyl (Boc)protecting group from a peptide?
(Multiple Choice)
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Draw the structure of the product of the following reaction and describe the usefulness of this type of reaction.
(Essay)
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To what structural feature does the term "secondary structure" refer?
(Multiple Choice)
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Match a structure from the list below to each of the following terms.
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(Essay)
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Refer to the data below to answer the following question.
-Refer to instructions.At what pH would you carry out an electrophoresis experiment if you wanted to separate a mixture of lysine,aspartic acid and phenylalanine? Explain.
(Essay)
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Which of the following tripeptides is not hydrolysed by trypsin?
(Multiple Choice)
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Refer to the data below to answer the following question(s).
Porcine dynorphin is a neuropeptide having 17 amino acid residues.Its structure is shown below.
Tyr-Gly-Gly-Phe-Leu-Arg-Arg-Ile-Arg-Pro-Lys-Leu-Lys-Trp-Asp-Asn-Gln
-Refer to instructions.Show the steps involved in a synthesis of F-G-I using the Merrifield procedure.
(Essay)
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To what structural feature does the term "primary structure" refer?
(Multiple Choice)
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Instructions: Match a term from the list below to each definition.

(Short Answer)
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How does phenyl isothiocyanate,Ph-N=C=S,react with a peptide in the Edman degradation?
(Multiple Choice)
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Which of the following amino acids migrates to the positive electrode on paper electrophoresis at a pH of 7.0?
(Multiple Choice)
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