Filters
Question type

Study Flashcards

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


A) Cysteine
B) Alanine
C) Tyrosine
D) Isoleucine

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

Correct Answer

verifed

verified

What is the product of the following reaction? (Assume workup to neutralize.) What is the product of the following reaction? (Assume workup to neutralize.)    A) I B) II C) III D) IV


A) I
B) II
C) III
D) IV

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

Correct Answer

verifed

verified

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

Correct Answer

verifed

verified

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? 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?   A) (R) -Phenylalanine is produced since the acylase only hydrolyzes the amides of L-amino acids. B) (S) -Phenylalanine is produced since the acylase only hydrolyzes the amides of L-amino acids. C) (R) -Phenylalanine is produced since the acylase only hydrolyzes the amides of D-amino acids. D) (S) -Phenylalanine is produced since the acylase only hydrolyzes the amides of D-amino acids.


A) (R) -Phenylalanine is produced since the acylase only hydrolyzes the amides of L-amino acids.
B) (S) -Phenylalanine is produced since the acylase only hydrolyzes the amides of L-amino acids.
C) (R) -Phenylalanine is produced since the acylase only hydrolyzes the amides of D-amino acids.
D) (S) -Phenylalanine is produced since the acylase only hydrolyzes the amides of D-amino acids.

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

Correct Answer

verifed

verified

What amino acid is at the N-terminus of the following peptide? What amino acid is at the N-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 C)

Correct Answer

verifed

verified

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 D)
F) B) and D)

Correct Answer

verifed

verified

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) None of the above

Correct Answer

verifed

verified

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) A) and D)
F) C) and D)

Correct Answer

verifed

verified

What are the basic steps in the Merrifield peptide synthesis?


A) Coupling and hydrolysis
B) Hydrolysis and deprotection
C) Deprotection and hydrogenation
D) Coupling and deprotection

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

Correct Answer

verifed

verified

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

Correct Answer

verifed

verified

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

Correct Answer

verifed

verified

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 D)
F) A) and B)

Correct Answer

verifed

verified

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


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

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

Correct Answer

verifed

verified

C

Which of the following correctly describes a protein?


A) a dipeptide; two amino acids joined together by one amide bond
B) a tripeptide; three amino acids joined together by two amide bonds
C) a polymer of more than 40 amino acids joined together by amide bonds
D) a polypeptide of any number of amino acids joined together by amide bonds

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

Correct Answer

verifed

verified

Which of the following is (are) globular protein(s) ?


A) Hemoglobin
B) Keratins
C) Collagens
D) Elastins

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

Correct Answer

verifed

verified

A

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) All of the above

Correct Answer

verifed

verified

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. 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 A) 1=Lys,2=Thr,3=Glu,4=Trp,5=Ile B) 1=Glu,2=Thr,3=Lys,4=Trp,5=Ile C) 1=Lys,2=Ile,3=Glu,4=Trp,5=Thr D) 1=Glu,2=Ile,3=Lys,4=Trp,5=Thr amino acid-pI value Trp-5.9 Glu-3.2 Lys-9.7 Ile-6.0 Thr-5.6


A) 1=Lys,2=Thr,3=Glu,4=Trp,5=Ile
B) 1=Glu,2=Thr,3=Lys,4=Trp,5=Ile
C) 1=Lys,2=Ile,3=Glu,4=Trp,5=Thr
D) 1=Glu,2=Ile,3=Lys,4=Trp,5=Thr

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

Correct Answer

verifed

verified

What is the appropriate sequence of reaction conditions used to synthesize valine from acetamidomalonic ester? What is the appropriate sequence of reaction conditions used to synthesize valine from acetamidomalonic ester?   A) (1) NaOH; (2) (CH<sub>3</sub>) <sub>2</sub>CHBr; (3) Cl<sub>2</sub>,H<sub>2</sub>O,heat B) (1) NaOCH<sub>2</sub>CH<sub>3</sub>; (2) (CH<sub>3</sub>) <sub>2</sub>CH<sub>2</sub>CHBr; (3) HCl,H<sub>2</sub>O,heat C) (1) NaOCH<sub>2</sub>CH<sub>3</sub>; (2) (CH<sub>3</sub>) <sub>2</sub>CHBr; (3) HCl,H<sub>2</sub>O,heat D) (1) NaOH; (2) CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>Br; (3) HCl,H<sub>2</sub>O,heat


A) (1) NaOH; (2) (CH3) 2CHBr; (3) Cl2,H2O,heat
B) (1) NaOCH2CH3; (2) (CH3) 2CH2CHBr; (3) HCl,H2O,heat
C) (1) NaOCH2CH3; (2) (CH3) 2CHBr; (3) HCl,H2O,heat
D) (1) NaOH; (2) CH3CH2CH2Br; (3) HCl,H2O,heat

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

Correct Answer

verifed

verified

What reagents would you use to convert acetaldehyde into alanine?


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

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

Correct Answer

verifed

verified

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

Correct Answer

verifed

verified

A

Showing 1 - 20 of 46

Related Exams

Show Answer