Deck 25: Amino Acids, Peptides, and Proteins

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

A)
<strong>Which of the following is the zwitterion form of L-alanine? </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B)
<strong>Which of the following is the zwitterion form of L-alanine? </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C)
<strong>Which of the following is the zwitterion form of L-alanine? </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D)
<strong>Which of the following is the zwitterion form of L-alanine? </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
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Question
What is the pI of valine, shown below? (the pKa\mathrm{p} K_{\mathrm{a}} 's are shown)
 <strong>What is the pI of valine, shown below? (the  \mathrm{p} K_{\mathrm{a}}  's are shown)  </strong> A) 2.32 B) 4.81 C) 5.97 D) 9.62 <div style=padding-top: 35px>

A) 2.32
B) 4.81
C) 5.97
D) 9.62
Question
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)
 <strong>Which of the following is the major product of the reaction shown below? (the  \mathrm{p} K_{\mathrm{a}}{ }^{\text {'s }}  are shown)  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A)
 <strong>Which of the following is the major product of the reaction shown below? (the  \mathrm{p} K_{\mathrm{a}}{ }^{\text {'s }}  are shown)  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B)
 <strong>Which of the following is the major product of the reaction shown below? (the  \mathrm{p} K_{\mathrm{a}}{ }^{\text {'s }}  are shown)  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C)
 <strong>Which of the following is the major product of the reaction shown below? (the  \mathrm{p} K_{\mathrm{a}}{ }^{\text {'s }}  are shown)  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D)
 <strong>Which of the following is the major product of the reaction shown below? (the  \mathrm{p} K_{\mathrm{a}}{ }^{\text {'s }}  are shown)  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
The Fischer projection shown below denotes a amino acid which has the configuration.
<strong>The Fischer projection shown below denotes a amino acid which has the configuration.  </strong> A) D, S B) D, R C) L, S D) L, R <div style=padding-top: 35px>

A) D, S
B) D, R
C) L, S
D) L, R
Question
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
Question
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
Question
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?
 <strong>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?  </strong> A) A B) B C) C D) D <div style=padding-top: 35px>

A) A
B) B
C) C
D) D
Question
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.
Question
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
Question
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
Question
Which of the following is the DNP derivative obtained from the reaction sequence shown below?
<strong>Which of the following is the DNP derivative obtained from the reaction sequence shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A)
<strong>Which of the following is the DNP derivative obtained from the reaction sequence shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B)
<strong>Which of the following is the DNP derivative obtained from the reaction sequence shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C)
<strong>Which of the following is the DNP derivative obtained from the reaction sequence shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D)
<strong>Which of the following is the DNP derivative obtained from the reaction sequence shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
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
Question
Which one of the following is the final product of the reaction sequence shown below? <strong>Which one of the following is the final product of the reaction sequence shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A)
<strong>Which one of the following is the final product of the reaction sequence shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B)
<strong>Which one of the following is the final product of the reaction sequence shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C)
<strong>Which one of the following is the final product of the reaction sequence shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D)
<strong>Which one of the following is the final product of the reaction sequence shown below?  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)
<strong>Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A)
<strong>Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B)
<strong>Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C)
<strong>Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D)
<strong>Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
In aqueous solution, the artificial sweetener aspartame slowly converts to the cyclic compound shown below. Which of the following best describes this reaction?  <strong>In aqueous solution, the artificial sweetener aspartame slowly converts to the cyclic compound shown below. Which of the following best describes this reaction?  </strong> A) nucleophilic acyl substitution B) Dieckmann condensation C) ester hydrolysis D)  \mathrm{S}_{\mathrm{N}} 2  reaction <div style=padding-top: 35px>

A) nucleophilic acyl substitution
B) Dieckmann condensation
C) ester hydrolysis
D) SN2\mathrm{S}_{\mathrm{N}} 2 reaction
Question
Which of the following is the abbreviated formula of the tetrapeptide shown below? (Hint: Remember to start at the N\mathrm{N} -terminal end.)
 <strong>Which of the following is the abbreviated formula of the tetrapeptide shown below? (Hint: Remember to start at the  \mathrm{N} -terminal end.)   </strong> A) lys-ser-asp-ala B) ser-lys-ala-asp C) asp-ala-ser-lys D) asp-ser-ala-lys <div style=padding-top: 35px>

A) lys-ser-asp-ala
B) ser-lys-ala-asp
C) asp-ala-ser-lys
D) asp-ser-ala-lys
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Deck 25: Amino Acids, Peptides, and Proteins
1
Which of the following is the zwitterion form of L-alanine?

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

2
What is the pI of valine, shown below? (the pKa\mathrm{p} K_{\mathrm{a}} 's are shown)
 <strong>What is the pI of valine, shown below? (the  \mathrm{p} K_{\mathrm{a}}  's are shown)  </strong> A) 2.32 B) 4.81 C) 5.97 D) 9.62

A) 2.32
B) 4.81
C) 5.97
D) 9.62
5.97
3
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)
 <strong>Which of the following is the major product of the reaction shown below? (the  \mathrm{p} K_{\mathrm{a}}{ }^{\text {'s }}  are shown)  </strong> A)   B)   C)   D)

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

4
The Fischer projection shown below denotes a amino acid which has the configuration.
<strong>The Fischer projection shown below denotes a amino acid which has the configuration.  </strong> A) D, S B) D, R C) L, S D) L, R

A) D, S
B) D, R
C) L, S
D) L, R
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5
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
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6
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
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7
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?
 <strong>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?  </strong> A) A B) B C) C D) D

A) A
B) B
C) C
D) D
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8
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.
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9
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
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10
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
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11
Which of the following is the DNP derivative obtained from the reaction sequence shown below?
<strong>Which of the following is the DNP derivative obtained from the reaction sequence shown below?  </strong> A)   B)   C)   D)

A)
<strong>Which of the following is the DNP derivative obtained from the reaction sequence shown below?  </strong> A)   B)   C)   D)
B)
<strong>Which of the following is the DNP derivative obtained from the reaction sequence shown below?  </strong> A)   B)   C)   D)
C)
<strong>Which of the following is the DNP derivative obtained from the reaction sequence shown below?  </strong> A)   B)   C)   D)
D)
<strong>Which of the following is the DNP derivative obtained from the reaction sequence shown below?  </strong> A)   B)   C)   D)
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12
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
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13
Which one of the following is the final product of the reaction sequence shown below? <strong>Which one of the following is the final product of the reaction sequence shown below?  </strong> A)   B)   C)   D)

A)
<strong>Which one of the following is the final product of the reaction sequence shown below?  </strong> A)   B)   C)   D)
B)
<strong>Which one of the following is the final product of the reaction sequence shown below?  </strong> A)   B)   C)   D)
C)
<strong>Which one of the following is the final product of the reaction sequence shown below?  </strong> A)   B)   C)   D)
D)
<strong>Which one of the following is the final product of the reaction sequence shown below?  </strong> A)   B)   C)   D)
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14
Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)
<strong>Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)  </strong> A)   B)   C)   D)

A)
<strong>Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)  </strong> A)   B)   C)   D)
B)
<strong>Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)  </strong> A)   B)   C)   D)
C)
<strong>Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)  </strong> A)   B)   C)   D)
D)
<strong>Identify the missing starting reagent needed in the Strecker synthesis of isoleucine. (Assume you will get all the stereoisomers of isoleucine.)  </strong> A)   B)   C)   D)
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15
In aqueous solution, the artificial sweetener aspartame slowly converts to the cyclic compound shown below. Which of the following best describes this reaction?  <strong>In aqueous solution, the artificial sweetener aspartame slowly converts to the cyclic compound shown below. Which of the following best describes this reaction?  </strong> 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
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16
Which of the following is the abbreviated formula of the tetrapeptide shown below? (Hint: Remember to start at the N\mathrm{N} -terminal end.)
 <strong>Which of the following is the abbreviated formula of the tetrapeptide shown below? (Hint: Remember to start at the  \mathrm{N} -terminal end.)   </strong> 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
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