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Which of the following compounds will show a broad absorption near 3300 cm-1 and a sharp absorption at 1650 cm-1? Which of the following compounds will show a broad absorption near 3300 cm<sup>-1</sup> and a sharp absorption at 1650 cm<sup>-1</sup>?   A)  I B)  II C)  III D)  IV E)  V


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

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Which of the following is true about the IR spectrum of the compound shown below? Which of the following is true about the IR spectrum of the compound shown below?   A)  absorptions at 1720 cm<sup>-1</sup> and 2150 cm<sup>-1</sup> B)  absorptions at 1800 cm<sup>-1</sup> and 2150 cm<sup>-1</sup> C)  absorptions at 1720 cm<sup>-1</sup> and 2250 cm<sup>-1</sup> D)  absorptions at 1800 cm<sup>-1</sup> and 2250 cm<sup>-1</sup> E)  absorptions at 1650 cm<sup>-1</sup> and 2150 cm<sup>-1</sup>


A) absorptions at 1720 cm-1 and 2150 cm-1
B) absorptions at 1800 cm-1 and 2150 cm-1
C) absorptions at 1720 cm-1 and 2250 cm-1
D) absorptions at 1800 cm-1 and 2250 cm-1
E) absorptions at 1650 cm-1 and 2150 cm-1

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Which of the following information is primarily obtained from infrared spectroscopy?


A) arrangement of carbon and hydrogen atoms in a compound
B) molecular weight of a compound
C) any conjugated π system present in a compound
D) functional groups present in a compound
E) all of these

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For each of the following IR spectra determine if it is consistent with the structure of an alcohol, a ketone, an aldehyde, a carboxylic acid, a primary amine, a secondary amine, a primary amide, or a secondary amide. For each of the following IR spectra determine if it is consistent with the structure of an alcohol, a ketone, an aldehyde, a carboxylic acid, a primary amine, a secondary amine, a primary amide, or a secondary amide.   I. SDBS: National Institute of Advanced Industrial Science and Technology II.  I. SDBS: National Institute of Advanced Industrial Science and Technology II. For each of the following IR spectra determine if it is consistent with the structure of an alcohol, a ketone, an aldehyde, a carboxylic acid, a primary amine, a secondary amine, a primary amide, or a secondary amide.   I. SDBS: National Institute of Advanced Industrial Science and Technology II.

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I: seconda...

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For the following reaction, which of the following change(s) in the IR spectrum is consistent with conversion of the reactant to the product? For the following reaction, which of the following change(s)  in the IR spectrum is consistent with conversion of the reactant to the product?   A)  absorption at 2250 cm<sup>-1</sup> should disappear B)  absorption at 3200-3400 cm<sup>-1</sup> and 1720cm<sup>-1</sup> should appear C)  absorption at 2250 cm<sup>-1</sup> should disappear, new absorptions at 2600-2800 cm<sup>-1</sup> and 1720 cm<sup>-1 </sup>should appear. D)  absorption at 2250 cm<sup>-1</sup> should disappear, a new absorption around 3400 cm<sup>-1</sup> should appear. E)  none of these


A) absorption at 2250 cm-1 should disappear
B) absorption at 3200-3400 cm-1 and 1720cm-1 should appear
C) absorption at 2250 cm-1 should disappear, new absorptions at 2600-2800 cm-1 and 1720 cm-1 should appear.
D) absorption at 2250 cm-1 should disappear, a new absorption around 3400 cm-1 should appear.
E) none of these

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Which of the following mass spectra shows the presence of bromine in a compound? I Which of the following mass spectra shows the presence of bromine in a compound? I   II   III   IV   Four spectra above: courtesy of SDBS: National Institute of Advanced Industrial Science and Technology A)  I B)  II C)  III D)  IV E)  none of these II Which of the following mass spectra shows the presence of bromine in a compound? I   II   III   IV   Four spectra above: courtesy of SDBS: National Institute of Advanced Industrial Science and Technology A)  I B)  II C)  III D)  IV E)  none of these III Which of the following mass spectra shows the presence of bromine in a compound? I   II   III   IV   Four spectra above: courtesy of SDBS: National Institute of Advanced Industrial Science and Technology A)  I B)  II C)  III D)  IV E)  none of these IV Which of the following mass spectra shows the presence of bromine in a compound? I   II   III   IV   Four spectra above: courtesy of SDBS: National Institute of Advanced Industrial Science and Technology A)  I B)  II C)  III D)  IV E)  none of these Four spectra above: courtesy of SDBS: National Institute of Advanced Industrial Science and Technology


A) I
B) II
C) III
D) IV
E) none of these

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Which of the following is true about the molecular weight and the M+•-m/z value for the following compound? Which of the following is true about the molecular weight and the M<sup>+</sup>•-m/z value for the following compound?   A)  odd molecular weight, m/z = 115 B)  odd molecular weight, m/z = 121 C)  even molecular weight, m/z = 96 D)  even molecular weight, m/z = 132 E)  even molecular weight, m/z = 116


A) odd molecular weight, m/z = 115
B) odd molecular weight, m/z = 121
C) even molecular weight, m/z = 96
D) even molecular weight, m/z = 132
E) even molecular weight, m/z = 116

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Which of the following is initially produced when a compound is bombarded with high energy electrons?


A) anions
B) free radicals
C) radical cations
D) cations
E) isotopes

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Define retention time.


A) the amount of time that the substance takes to boil
B) the amount of time that the substance takes to melt
C) the amount of time required to exit from the mass spectrometer
D) the amount of time required to exit from the gas chromatograph
E) the amount of time required to set up the GC-MS

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Carboxylic acids show a very broad absorption for the OH group compared to alcohols, because they can form a ______.


A) dimer
B) polymer
C) trimer
D) tetramer

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Why does bromine produces M+• and (M+2) +• peaks of equal intensity on a mass spectrum?


A) ADVANCE \u 281 ADVANCE \d 2Br isotope has higher natural abundance than ADVANCE \u 279 ADVANCE \d 2Br isotope
B) ADVANCE \u 279 ADVANCE \d 2Br and ADVANCE \u 281 ADVANCE \d 2Br isotopes have almost equal natural abundance
C) ADVANCE \u 279 ADVANCE \d 2Br isotope has higher natural abundance than ADVANCE \u 281 ADVANCE \d 2Br isotope
D) none of these

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Rank absorption of the indicated bonds in decreasing (highest to lowest) order of wavenumber. Rank absorption of the indicated bonds in decreasing (highest to lowest)  order of wavenumber.   A)  III > II > I B)  I > II > III C)  II > I > III D)  III > I > II E)  II > III > I


A) III > II > I
B) I > II > III
C) II > I > III
D) III > I > II
E) II > III > I

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Which one of the following compounds is consistent with the mass spectrum below? Which one of the following compounds is consistent with the mass spectrum below?   SDBS: National Institute of Advanced Industrial Science and Technology A)  CH<sub>3</sub>CH<sub>2</sub>CH(CH<sub>3</sub>) <sub>2</sub> B)  CH<sub>3</sub>CHOHCH<sub>2</sub>CH<sub>3</sub> C)  CH<sub>3</sub>CH<sub>2</sub>OCH<sub>2</sub>CH<sub>3</sub> D)  CH<sub>3</sub>CH<sub>2</sub>NHCH<sub>2</sub>CH<sub>3</sub> E)  CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> SDBS: National Institute of Advanced Industrial Science and Technology


A) CH3CH2CH(CH3) 2
B) CH3CHOHCH2CH3
C) CH3CH2OCH2CH3
D) CH3CH2NHCH2CH3
E) CH3CH2CH2CH3

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Which molecular formula is consistent with the following mass spectral data? M+ at m/z = 78, relative height = 23.5% (M+1) + at m/z = 79, relative height = 0.78% (M+2) + at m/z = 80, relative height = 7.5%


A) C6H6
B) C3H7Cl
C) C6H8
D) C6H9Cl
E) none of these

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Which of the following is not a prominent peak in the mass spectrum of 2-methyl-2-pentanol?


A) (M-15)
B) (M-18)
C) (M-29)
D) (M-16)
E) none of these

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Which of the following is not true about the molecular ion in mass spectrometry?


A) The molecular ion is produced by loss of one electron from the molecule.
B) The mass of the molecular ion is equivalent to the mass of the molecule.
C) The ion is produced by a loss of pair of electrons from the molecule.
D) The molecular ion is often unstable and can undergo fragmentation.

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Predict the product for the following reaction and explain how you can use IR spectroscopy to monitor the progress of the reaction. Predict the product for the following reaction and explain how you can use IR spectroscopy to monitor the progress of the reaction.

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blured image_TB4454_00 Absorptions for C=O...

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Which of the following mass spectra shows the presence of chlorine in a compound? I Which of the following mass spectra shows the presence of chlorine in a compound? I   II   III   IV   Four spectra above: courtesy of SDBS: National Institute of Advanced Industrial Science and Technology A)  I B)  II C)  III D)  IV E)  none of these II Which of the following mass spectra shows the presence of chlorine in a compound? I   II   III   IV   Four spectra above: courtesy of SDBS: National Institute of Advanced Industrial Science and Technology A)  I B)  II C)  III D)  IV E)  none of these III Which of the following mass spectra shows the presence of chlorine in a compound? I   II   III   IV   Four spectra above: courtesy of SDBS: National Institute of Advanced Industrial Science and Technology A)  I B)  II C)  III D)  IV E)  none of these IV Which of the following mass spectra shows the presence of chlorine in a compound? I   II   III   IV   Four spectra above: courtesy of SDBS: National Institute of Advanced Industrial Science and Technology A)  I B)  II C)  III D)  IV E)  none of these Four spectra above: courtesy of SDBS: National Institute of Advanced Industrial Science and Technology


A) I
B) II
C) III
D) IV
E) none of these

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Identify the medical application that does not use mass spectrometry.


A) cancer detection
B) metabolic defects in babies
C) pathogenic bacteria
D) drug analysis
E) all of these applications use mass spectrometry

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Provide a molecular formula that is consistent with the following mass spectral data. M+ at m/z = 73, relative height = 86.1% (M+1)+ at m/z = 74, relative height = 3.2%

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