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Instructions: Select the most reasonable formula for the compounds with the following mass spectral data. Refer to instructions.M+ at m/z = 216


A) C6H13OCl
B) C4H8Br2
C) C10H16
D) C9H12O

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

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At what approximate positions might the compound below show IR absorptions?At what approximate positions might the compound below show IR absorptions?

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This compound should show a me...

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Instructions: Refer to the mass spectrum of 2-methylbutane shown below to answer the following question(s). Instructions: Refer to the mass spectrum of 2-methylbutane shown below to answer the following question(s).    (Spectrum obtained from:SDBSWeb:http://www.aist.go.jp/RIODB/SDBS/)  -Refer to instructions.What peak represents the base peak? (Spectrum obtained from:SDBSWeb:http://www.aist.go.jp/RIODB/SDBS/) -Refer to instructions.What peak represents the base peak?

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The peak a...

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Which of the following does not involve the interaction of molecules with electromagnetic energy?


A) mass spectrometry
B) infrared spectroscopy
C) ultraviolet spectroscopy
D) nuclear magnetic resonance spectroscopy

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

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Which of the following bonds gives rise to a strong absorbance near 1700 cm-1 in the infrared spectrum?


A) C=O
B) C-O
C) C=C
D) C-C

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

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The amount of energy in infrared light corresponds to:


A) the amount of energy needed to promote one electron from a bonding to an antibonding molecular orbital
B) the amount of energy needed to fragment a molecule
C) the amount of energy needed to strip a molecule of one electron to generate a cation radical
D) the amount of energy needed to increase certain molecular motions,such as bond vibrations,in organic molecules

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

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Which of the following statements best describes the base peak in a mass spectrum?


A) The peak from the most stable radical.
B) The peak from the species that has the isotope with the highest atomic number.
C) The peak of highest intensity.
D) The peak from the molecule minus an electron.
E) The M +1 peak

F) A) and B)
G) A) and C)

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Cyclohexene and hex-2-yne both have the molecular formula,C6H10. a)How would you use infrared spectroscopy to distinguish between the two compounds? b)How could the mass spectrum be used to distinguish between the two compounds?

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What are the masses of the charged fragments produced by the dehydration of the following compound?What are the masses of the charged fragments produced by the dehydration of the following compound?

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This compound has the formula ...

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Which of the following peaks is not prominent in the mass spectrum of 2-methylbutan-2-ol?


A) M+ - 15
B) M+ - 18
C) M+ - 21
D) M+ - 29

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

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Instructions: Refer to the mass spectrum of 2-methylbutane shown below to answer the following question(s). Instructions: Refer to the mass spectrum of 2-methylbutane shown below to answer the following question(s).    (Spectrum obtained from:SDBSWeb:http://www.aist.go.jp/RIODB/SDBS/)  -Refer to instructions.Propose structures for fragment ions at m/z = 57,43,and 29. (Spectrum obtained from:SDBSWeb:http://www.aist.go.jp/RIODB/SDBS/) -Refer to instructions.Propose structures for fragment ions at m/z = 57,43,and 29.

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Which of the following compounds gives an infrared spectrum with a peak at ~1750 cm-1,but no significant peaks at 3000-3500 cm-1 or 1050-1250 cm-1?


A) Which of the following compounds gives an infrared spectrum with a peak at ~1750 cm<sup>-1</sup>,but no significant peaks at 3000-3500 cm<sup>-1</sup> or 1050-1250 cm<sup>-1</sup>? A)    B)    C)    D)
B) Which of the following compounds gives an infrared spectrum with a peak at ~1750 cm<sup>-1</sup>,but no significant peaks at 3000-3500 cm<sup>-1</sup> or 1050-1250 cm<sup>-1</sup>? A)    B)    C)    D)
C) Which of the following compounds gives an infrared spectrum with a peak at ~1750 cm<sup>-1</sup>,but no significant peaks at 3000-3500 cm<sup>-1</sup> or 1050-1250 cm<sup>-1</sup>? A)    B)    C)    D)
D) Which of the following compounds gives an infrared spectrum with a peak at ~1750 cm<sup>-1</sup>,but no significant peaks at 3000-3500 cm<sup>-1</sup> or 1050-1250 cm<sup>-1</sup>? A)    B)    C)    D)

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

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Which of the following bonds undergoes stretching at the highest frequency?


A) O-H
B) C-H
C) C=O
D) CºC

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

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Consider the compound below:Consider the compound below:   a)At what approximate positions might the compound show IR absorptions? 	  b)How would this spectrum differ from that of cyclohexanol? a)At what approximate positions might the compound show IR absorptions? b)How would this spectrum differ from that of cyclohexanol?

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What is the horizontal axis of a mass spectrum?


A) mass
B) mass/energy
C) mass/charge
D) charge

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

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Which of the following regions in the electromagnetic spectrum corresponds to the radiation with the highest energy?


A) radio waves
B) ultraviolet
C) infrared
D) visible

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

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Instructions: Select the most reasonable formula for the compounds with the following mass spectral data. Refer to instructions.M+ at m/z = 101


A) C5H6Br
B) C5H12N2
C) C6H15N
D) C9H12O

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

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Match a structure from the list below to the following IR spectra. -Match a structure from the list below to the following IR spectra. -

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What are the units for electromagnetic radiation used in infrared spectroscopy?


A) cm
B) cm-1
C) J.mol-1
D) none,wavenumber is a dimensionless quantity

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

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A 3.42 ´ 10-5 M solution of dibenzalacetone in ethanol produced an absorbance of 0.753 in a 1.00 cm cell.Based on this data,what is e for this compound?


A) 2.57 ´ 105
B) 2.20 ´ 104
C) 4.54 ´ 10-5
D) 2.92 ´ 104

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

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