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Which of the following protons gives an NMR signal with the lowest chemical shift value (farthest upfield) ? Which of the following protons gives an NMR signal with the lowest chemical shift value (farthest upfield) ?   A) 1 B) 2 C) 3 D) 4 E) 5


A) 1
B) 2
C) 3
D) 4
E) 5

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How many proton NMR singlets will 2-bromo-3-methyl-2-butene exhibit?


A) 1
B) 2
C) 3
D) 4
E) 5

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Deduce the identity of the following compound from the 1H NMR spectral data given. C3H6Br2 : two peaks: a 2H quintet and a 4H triplet

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Which compound has a 1H NMR spectrum consisting of the following peaks: 0.9 (6H, d) , 1.0 (3H, t) , 2.2 (2H, q) , and 4.0 (1H, septet) ?


A) (CH3) 2CHCH2O2CCH3
B) (CH3) 2CHCH2CO2CH3
C) (CH3) 2CHO2CCH2CH3
D) (CH3) 2CHCO2CH2CH3
E) (CH3) 2CHOCH2CH3

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Give the structure of a compound that has a formula of C8H11N and has signals in the 13C NMR spectrum at 25.9 ppm (CH3) , 51.1 ppm (CH) , 125.9 ppm (CH) , 126.6 ppm (CH) , 128.3 ppm (CH) , and 148.5 ppm (C) .


A) Give the structure of a compound that has a formula of C<sub>8</sub>H<sub>11</sub>N and has signals in the <sup>13</sup>C NMR spectrum at 25.9 ppm (CH<sub>3</sub>) , 51.1 ppm (CH) , 125.9 ppm (CH) , 126.6 ppm (CH) , 128.3 ppm (CH) , and 148.5 ppm (C) . A)    B)    C)    D)    E)
B) Give the structure of a compound that has a formula of C<sub>8</sub>H<sub>11</sub>N and has signals in the <sup>13</sup>C NMR spectrum at 25.9 ppm (CH<sub>3</sub>) , 51.1 ppm (CH) , 125.9 ppm (CH) , 126.6 ppm (CH) , 128.3 ppm (CH) , and 148.5 ppm (C) . A)    B)    C)    D)    E)
C) Give the structure of a compound that has a formula of C<sub>8</sub>H<sub>11</sub>N and has signals in the <sup>13</sup>C NMR spectrum at 25.9 ppm (CH<sub>3</sub>) , 51.1 ppm (CH) , 125.9 ppm (CH) , 126.6 ppm (CH) , 128.3 ppm (CH) , and 148.5 ppm (C) . A)    B)    C)    D)    E)
D) Give the structure of a compound that has a formula of C<sub>8</sub>H<sub>11</sub>N and has signals in the <sup>13</sup>C NMR spectrum at 25.9 ppm (CH<sub>3</sub>) , 51.1 ppm (CH) , 125.9 ppm (CH) , 126.6 ppm (CH) , 128.3 ppm (CH) , and 148.5 ppm (C) . A)    B)    C)    D)    E)
E) Give the structure of a compound that has a formula of C<sub>8</sub>H<sub>11</sub>N and has signals in the <sup>13</sup>C NMR spectrum at 25.9 ppm (CH<sub>3</sub>) , 51.1 ppm (CH) , 125.9 ppm (CH) , 126.6 ppm (CH) , 128.3 ppm (CH) , and 148.5 ppm (C) . A)    B)    C)    D)    E)

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Give one reason why 13C NMR is less sensitive than 1H NMR.

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Natural isotopic abundance of ...

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How many signals would you expect to see in the 1H NMR spectrum of the following compound? How many signals would you expect to see in the <sup>1</sup>H NMR spectrum of the following compound?   A) 5 B) 4 C) 2 D) 3 E) 1


A) 5
B) 4
C) 2
D) 3
E) 1

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Which of the following electromagnetic wave types is used in nuclear magnetic resonance spectroscopy?


A) X-ray
B) infrared
C) visible
D) radio
E) ultraviolet

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Deduce the identity of the following compound from the spectral data given. C5H10O: 1H NMR, Ī“ 1.2 (6H, doublet), 2.1 (3H, singlet), 2.8 (1H, septet); IR, 2980, 1710 cm-1; MS, m/z 71,

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What information does a HETCOR spectrum give?

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Coupling between hydrogens and the hydrogens to which they are attached to.

If a chemical shift of an NMR signal is 7.2 ppm measured in a 60 MHz NMR spectrometer, how many Hz would this signal be from the TMS signal?


A) 8) 3 Hz
B) 432 Hz
C) 0) 12 Hz
D) 72 Hz
E) 60 Hz

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How many signals would you expect to see in the 1H NMR spectrum of the following compound? How many signals would you expect to see in the <sup>1</sup>H NMR spectrum of the following compound?   A) 1 B) 2 C) 3 D) 4 E) 5


A) 1
B) 2
C) 3
D) 4
E) 5

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What splitting pattern is observed in the proton NMR spectrum for the indicated hydrogens? What splitting pattern is observed in the proton NMR spectrum for the indicated hydrogens?   A) singlet B) doublet C) triplet D) quartet E) septet


A) singlet
B) doublet
C) triplet
D) quartet
E) septet

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A

Why is Fourier transform NMR spectroscopy preferred over continuous wave as a technique for 13C NMR?

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13C nuclei have a low sensitivity which re...

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What splitting pattern is observed in the proton NMR spectrum for the indicated hydrogens? CH3OCH2CH2OCH3 ↑


A) singlet
B) doublet
C) triplet
D) quartet
E) septet

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A

How many signals would you expect to see in the 1H NMR spectrum of the following compound? ClCH2CH2Cl


A) 5
B) 4
C) 3
D) 2
E) 1

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How many distinct carbon signals are expected in the proton-decoupled 13C NMR spectrum of the compound below? How many distinct carbon signals are expected in the proton-decoupled <sup>13</sup>C NMR spectrum of the compound below?

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Deduce the identity of the following compound from the 1H NMR spectral data given. C8H18O : Ī“ 0.89 (6H, doublet), 1.87 (1H, multiplet), 3.17 (2H, doublet)(ppm)

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An unknown compound, C4H8Br2, gave the following proton NMR data: Singlet at 1.97 ppm (6H) Singlet at 3.89 ppm (2H) What is the compound?

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Give the structure of a compound that has a formula of C9H10O2 and has signals in the 13C NMR spectrum at 13.6 ppm (CH3) ; 59.1 ppm (CH2) ; 128.4 ppm (CH) ; 129.7 ppm (CH) ; 130.5 ppm (C) ; 132.8 ppm (CH) ; and167.0 ppm (C) .


A) Give the structure of a compound that has a formula of C<sub>9</sub>H<sub>10</sub>O<sub>2</sub> and has signals in the <sup>13</sup>C NMR spectrum at 13.6 ppm (CH<sub>3</sub>) ; 59.1 ppm (CH<sub>2</sub>) ; 128.4 ppm (CH) ; 129.7 ppm (CH) ; 130.5 ppm (C) ; 132.8 ppm (CH) ; and167.0 ppm (C) . A)    B)    C)    D)    E)
B) Give the structure of a compound that has a formula of C<sub>9</sub>H<sub>10</sub>O<sub>2</sub> and has signals in the <sup>13</sup>C NMR spectrum at 13.6 ppm (CH<sub>3</sub>) ; 59.1 ppm (CH<sub>2</sub>) ; 128.4 ppm (CH) ; 129.7 ppm (CH) ; 130.5 ppm (C) ; 132.8 ppm (CH) ; and167.0 ppm (C) . A)    B)    C)    D)    E)
C) Give the structure of a compound that has a formula of C<sub>9</sub>H<sub>10</sub>O<sub>2</sub> and has signals in the <sup>13</sup>C NMR spectrum at 13.6 ppm (CH<sub>3</sub>) ; 59.1 ppm (CH<sub>2</sub>) ; 128.4 ppm (CH) ; 129.7 ppm (CH) ; 130.5 ppm (C) ; 132.8 ppm (CH) ; and167.0 ppm (C) . A)    B)    C)    D)    E)
D) Give the structure of a compound that has a formula of C<sub>9</sub>H<sub>10</sub>O<sub>2</sub> and has signals in the <sup>13</sup>C NMR spectrum at 13.6 ppm (CH<sub>3</sub>) ; 59.1 ppm (CH<sub>2</sub>) ; 128.4 ppm (CH) ; 129.7 ppm (CH) ; 130.5 ppm (C) ; 132.8 ppm (CH) ; and167.0 ppm (C) . A)    B)    C)    D)    E)
E) Give the structure of a compound that has a formula of C<sub>9</sub>H<sub>10</sub>O<sub>2</sub> and has signals in the <sup>13</sup>C NMR spectrum at 13.6 ppm (CH<sub>3</sub>) ; 59.1 ppm (CH<sub>2</sub>) ; 128.4 ppm (CH) ; 129.7 ppm (CH) ; 130.5 ppm (C) ; 132.8 ppm (CH) ; and167.0 ppm (C) . A)    B)    C)    D)    E)

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