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Which of the following statements about 13C NMR is not true?


A) "In 13C proton-decoupled NMR spectra,all peaks are singlets."
B) "13C NMR spectra display peaks for only carbons that bear hydrogen atoms."
C) "13C NMR chemical shifts occur over a greater range than 1H NMR chemical shifts."
D) "13C NMR easily differentiates between the different hybridized carbons (sp3,sp2,and sp hybridized carbons) ."

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

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B

What effect does increasing the operating frequency of a 1H NMR spectrum have on the value of chemical shift in Δ?


A) Chemical shift in Δ will also increase.
B) Chemical shift in Δ will decrease.
C) Chemical shift in Δ will remain the same.
D) It is not possible to predict the change in chemical shift in Δ.

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

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Which of the labeled protons would absorb furthest downfield in a 1H NMR spectrum? Which of the labeled protons would absorb furthest downfield in a <sup>1</sup>H NMR spectrum?   A) I B) II C) III D) IV


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

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

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How many different kinds of protons are present in each of the following compounds? How many different kinds of protons are present in each of the following compounds?   A) I = 2; II = 3; III = 4 B) I = 2; II = 3; III = 3 C) I = 3; II = 3; III = 3 D) I = 3; II = 3; III = 4


A) I = 2; II = 3; III = 4
B) I = 2; II = 3; III = 3
C) I = 3; II = 3; III = 3
D) I = 3; II = 3; III = 4

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

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An unknown compound has the formula of C9H12.The following 1H NMR peaks were observed: Doublet at Δ 1.22 Septet at Δ 2.83 Multiplet at Δ 7.09 From the data above,pick the compound below that fits the spectra data. An unknown compound has the formula of C<sub>9</sub>H<sub>12</sub>.The following <sup>1</sup>H NMR peaks were observed: Doublet at Δ 1.22 Septet at Δ 2.83 Multiplet at Δ 7.09 From the data above,pick the compound below that fits the spectra data.   A) I B) II C) III D) IV


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

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

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An unknown compound A has the molecular formula C7H14O2.Compound A absorbs strongly in the IR at 1700 cm-1.The 1H NMR spectral data for compound A are given below.What is the structure of compound A? An unknown compound A has the molecular formula C<sub>7</sub>H<sub>14</sub>O<sub>2</sub>.Compound A absorbs strongly in the IR at 1700 cm<sup>-1</sup>.The <sup>1</sup>H NMR spectral data for compound A are given below.What is the structure of compound A?   A) I B) II C) III D) IV


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

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

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C

How many peaks would be observed for each of the circled protons in the compounds below? How many peaks would be observed for each of the circled protons in the compounds below?   A) I = 8; II = 4; III = 3; IV = 3 B) I = 7; II = 4; III = 3; IV = 4 C) I = 7; II = 3; III = 3; IV = 3 D) I = 7; II = 4; III = 2; IV = 4


A) I = 8; II = 4; III = 3; IV = 3
B) I = 7; II = 4; III = 3; IV = 4
C) I = 7; II = 3; III = 3; IV = 3
D) I = 7; II = 4; III = 2; IV = 4

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

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How many different kinds of protons are present in the following molecule? How many different kinds of protons are present in the following molecule?   A) 2 B) 3 C) 4 D) 5


A) 2
B) 3
C) 4
D) 5

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

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Which of the indicated protons would absorb furthest downfield in a 1H NMR spectrum? Which of the indicated protons would absorb furthest downfield in a <sup>1</sup>H NMR spectrum?   A) I B) II C) III D) IV


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

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

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How many different kinds of protons are present in each of the following compounds? How many different kinds of protons are present in each of the following compounds?   A) I = 6; II = 5; III = 3 B) I = 7; II = 5; III = 3 C) I = 7; II = 6; III = 3 D) I = 6; II = 6; III = 3


A) I = 6; II = 5; III = 3
B) I = 7; II = 5; III = 3
C) I = 7; II = 6; III = 3
D) I = 6; II = 6; III = 3

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

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Which of the following compounds does not show only one signal in its 1H NMR spectrum? Which of the following compounds does not show only one signal in its <sup>1</sup>H NMR spectrum?   A) I B) II C) III D) IV


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

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

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How many different kinds of protons are present in each of the following compounds? How many different kinds of protons are present in each of the following compounds?   A) a: 5; b: 6 B) a: 5; b: 5 C) a: 4; b: 6 D) a: 4; b: 5


A) a: 5; b: 6
B) a: 5; b: 5
C) a: 4; b: 6
D) a: 4; b: 5

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

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How many peaks would be observed for each of the circled protons in the compounds below? How many peaks would be observed for each of the circled protons in the compounds below?   A) I = 2; II = 6; III = 1 B) I = 3; II = 5; III = 2 C) I = 1; II = 5; III = 1 D) I = 2; II = 6; III = 2


A) I = 2; II = 6; III = 1
B) I = 3; II = 5; III = 2
C) I = 1; II = 5; III = 1
D) I = 2; II = 6; III = 2

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

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A

What effect does increasing the operating frequency of a 1H NMR spectrum have on the frequency of an absorption in Hz?


A) Frequency of an absorption in Hz will also increase.
B) Frequency of an absorption in Hz will decrease.
C) Frequency of an absorption in Hz will remain the same.
D) It is not possible to predict the change in frequency of an absorption in Hz.

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

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An unknown compound X has the molecular formula C10H11O2Br.Compound X shows a strong absorption in its IR spectrum at 1700 cm-1.The 1H NMR spectral data for compound X is given below.What is the structure of compound X? An unknown compound X has the molecular formula C<sub>10</sub>H<sub>11</sub>O<sub>2</sub>Br.Compound X shows a strong absorption in its IR spectrum at 1700 cm<sup>-1</sup>.The <sup>1</sup>H NMR spectral data for compound X is given below.What is the structure of compound X?   A) Only I B) Only II C) Only III D) I or II


A) Only I
B) Only II
C) Only III
D) I or II

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

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Which of the following spectroscopy methods does not involve the interaction of organic molecules with electromagnetic radiation?


A) Nuclear magnetic resonance
B) Infrared spectroscopy
C) Mass spectrometry
D) Ultraviolet spectroscopy

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

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Which of the following statements is true about electromagnetic radiation?


A) All molecules absorb electromagnetic radiation at some frequency.
B) Frequency is directly proportional to wavelength.
C) NMR uses the microwave region of the electromagnetic spectrum.
D) The radio frequency region of the electromagnetic spectrum has the largest energy per photon.
E) Energy is inversely proportional to frequency.

F) A) and E)
G) A) and B)

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An unknown compound A has the molecular formula C12H16O.Compound A absorbs strongly in the IR at 1700 cm-1.The NMR spectral data for compound A are given below.What is the structure of compound A? An unknown compound A has the molecular formula C<sub>12</sub>H<sub>16</sub>O.Compound A absorbs strongly in the IR at 1700 cm<sup>-1</sup>.The NMR spectral data for compound A are given below.What is the structure of compound A?   A) I B) II C) III D) IV


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

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

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Which of the labeled protons absorbs furthest upfield in the 1H NMR spectrum? Which of the labeled protons absorbs furthest upfield in the <sup>1</sup>H NMR spectrum?   A) H<sub>a</sub> B) H<sub>b</sub> C) H<sub>c</sub> D) H<sub>d</sub>


A) Ha
B) Hb
C) Hc
D) Hd

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

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How many peaks would be observed for each of the circled protons in the compounds below? How many peaks would be observed for each of the circled protons in the compounds below?   A) I = 1; II = 4; III = 7 B) I = 3; II = 3; III = 7 C) I = 2; II = 4; III = 7 D) I = 2; II = 4; III = 6


A) I = 1; II = 4; III = 7
B) I = 3; II = 3; III = 7
C) I = 2; II = 4; III = 7
D) I = 2; II = 4; III = 6

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

Correct Answer

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