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What is the net charge on the dipeptide lys-asp at a pH\mathrm{pH} of 1.0 ? Aspartic acid (R=CH2CO2H) \left(\mathrm{R}=-\mathrm{CH}_{2} \mathrm{CO}_{2} \mathrm{H}\right) Lysine ( R=CH2CH2CH2CH2NH2) \left.\mathrm{R}=\mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{NH}_{2}\right)


A) +1
B) +2
C) +3
D) +4

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

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Which of the following is the zwitterion form of L-alanine?


A)
Which of the following is the zwitterion form of L-alanine?  A)     B)    C)     D)
B)
Which of the following is the zwitterion form of L-alanine?  A)     B)    C)     D)
C)
Which of the following is the zwitterion form of L-alanine?  A)     B)    C)     D)
D)
Which of the following is the zwitterion form of L-alanine?  A)     B)    C)     D)

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

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Which one of the following is the final product of the reaction sequence shown below? Which one of the following is the final product of the reaction sequence shown below?   A)    B)     C)     D)


A)
Which one of the following is the final product of the reaction sequence shown below?   A)    B)     C)     D)
B)
Which one of the following is the final product of the reaction sequence shown below?   A)    B)     C)     D)
C)
Which one of the following is the final product of the reaction sequence shown below?   A)    B)     C)     D)
D)
Which one of the following is the final product of the reaction sequence shown below?   A)    B)     C)     D)

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

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B

A pentapeptide was found to contain the amino acids ala, gly, met, phe, and ser. Partial hydrolysis of the pentapeptide gave the dipeptides gly-ser, met-phe, ala-gly, and ser-met. What is the sequence of the pentapeptide?


A) gly-ser-met-phe-ala
B) gly-ser-met-ala-phe
C) ala-gly-ser-phe-met
D) ala-gly-ser-met-phe

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

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Which one of the following reagents is used for the visual detection of amino acids?


A) Sanger's reagent
B) dicyclohexylcarbodiimide (DCCI)
C) ninhydrin
D) phenyl isothiocyanate

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

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Which of the following is the major product of the reaction shown below? (the pKa’s \mathrm{p} K_{\mathrm{a}}{ }^{\text {'s }} are shown)  Which of the following is the major product of the reaction shown below? (the  \mathrm{p} K_{\mathrm{a}}{ }^{\text {'s }}  are shown)    A)     B)    C)     D)


A)
 Which of the following is the major product of the reaction shown below? (the  \mathrm{p} K_{\mathrm{a}}{ }^{\text {'s }}  are shown)    A)     B)    C)     D)
B)
 Which of the following is the major product of the reaction shown below? (the  \mathrm{p} K_{\mathrm{a}}{ }^{\text {'s }}  are shown)    A)     B)    C)     D)
C)
 Which of the following is the major product of the reaction shown below? (the  \mathrm{p} K_{\mathrm{a}}{ }^{\text {'s }}  are shown)    A)     B)    C)     D)
D)
 Which of the following is the major product of the reaction shown below? (the  \mathrm{p} K_{\mathrm{a}}{ }^{\text {'s }}  are shown)    A)     B)    C)     D)

E) None of the above
F) All of the above

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What is the net charge on L-aspartic acid (R=CH2CO2H) \left(\mathrm{R}=-\mathrm{CH}_{2} \mathrm{CO}_{2} \mathrm{H}\right) at a pH of 11.0 ?


A) +1
B) +2
C) -1
D) -2

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

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In strongly acidic solution L-lysine is primarily a dication as shown below. As the pH\mathrm{pH} is raised, which proton is lost to form the monocation?  In strongly acidic solution L-lysine is primarily a dication as shown below. As the  \mathrm{pH}  is raised, which proton is lost to form the monocation?   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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B

Which of the following is the DNP derivative obtained from the reaction sequence shown below? Which of the following is the DNP derivative obtained from the reaction sequence shown below?   A)    B)    C)     D)


A)
Which of the following is the DNP derivative obtained from the reaction sequence shown below?   A)    B)    C)     D)
B)
Which of the following is the DNP derivative obtained from the reaction sequence shown below?   A)    B)    C)     D)
C)
Which of the following is the DNP derivative obtained from the reaction sequence shown below?   A)    B)    C)     D)
D)
Which of the following is the DNP derivative obtained from the reaction sequence shown below?   A)    B)    C)     D)

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

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A

Linus Pauling is credited with describing the α\alpha -helix structure of a polypeptide. The α\alpha -helix is an example of a polypeptide's


A) primary structure.
B) secondary structure.
C) tertiary structure.
D) quaternary structure.

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

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Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.) Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)    A)      B)     C)     D)


A)
Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)    A)      B)     C)     D)
B)
Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)    A)      B)     C)     D)
C)
Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)    A)      B)     C)     D)
D)
Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)    A)      B)     C)     D)

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

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What is the total number of different tripeptides which can result from three different L-amino acids?


A) three
B) four
C) six
D) nine

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

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Which of the following is the abbreviated formula of the tetrapeptide shown below? (Hint: Remember to start at the N\mathrm{N} -terminal end.)  Which of the following is the abbreviated formula of the tetrapeptide shown below? (Hint: Remember to start at the  \mathrm{N} -terminal end.)     A)  lys-ser-asp-ala B)  ser-lys-ala-asp C)  asp-ala-ser-lys D)  asp-ser-ala-lys


A) lys-ser-asp-ala
B) ser-lys-ala-asp
C) asp-ala-ser-lys
D) asp-ser-ala-lys

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

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In aqueous solution, the artificial sweetener aspartame slowly converts to the cyclic compound shown below. Which of the following best describes this reaction?  In aqueous solution, the artificial sweetener aspartame slowly converts to the cyclic compound shown below. Which of the following best describes this reaction?   A)  nucleophilic acyl substitution B)  Dieckmann condensation C)  ester hydrolysis D)   \mathrm{S}_{\mathrm{N}} 2  reaction


A) nucleophilic acyl substitution
B) Dieckmann condensation
C) ester hydrolysis
D) SN2\mathrm{S}_{\mathrm{N}} 2 reaction

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

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The Fischer projection shown below denotes a amino acid which has the configuration. The Fischer projection shown below denotes a amino acid which has the configuration.   A)  D, S B)  D, R C)  L, S D)  L, R


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

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

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What is the pI of valine, shown below? (the pKa\mathrm{p} K_{\mathrm{a}} 's are shown)  What is the pI of valine, shown below? (the  \mathrm{p} K_{\mathrm{a}}  's are shown)    A)  2.32 B)  4.81 C)  5.97 D)  9.62


A) 2.32
B) 4.81
C) 5.97
D) 9.62

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

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