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For the following reaction, explain how you can use IR spectroscopy to monitor the progress of the reaction. For the following reaction, explain how you can use IR spectroscopy to monitor the progress of the reaction.

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The two absorptions at 3350 cm...

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Provide the structure of the major fragment that results when the molecular ion of (CH3)2CHCH2CH2NH2 undergoes fragmentation.

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Which one of the following compounds is consistent with the following IR spectrum? Which one of the following compounds is consistent with the following IR spectrum?   SDBS: National Institute of Advanced Industrial Science and Technology   A)  I B)  II C)  III D)  IV E)  V SDBS: National Institute of Advanced Industrial Science and Technology Which one of the following compounds is consistent with the following IR spectrum?   SDBS: National Institute of Advanced Industrial Science and Technology   A)  I B)  II C)  III D)  IV E)  V


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

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

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A compound with molecular formula C3H9N, shows absorptions at 3400 cm-1 (two), 2980 cm-1 and at 1100 cm-1 on the IR spectrum. Propose a possible structure for this compound.

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CH3CH2CH2NH2 O...

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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 or a secondary amine. I. 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 or a secondary amine. I.   SDBS: National Institute of Advanced Industrial Science and Technology II.   SDBS: National Institute of Advanced Industrial Science and Technology 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 or a secondary amine. I.   SDBS: National Institute of Advanced Industrial Science and Technology II.   SDBS: National Institute of Advanced Industrial Science and Technology SDBS: National Institute of Advanced Industrial Science and Technology

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I: aldehyd...

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A compound with molecular formula C6H10O, shows absorptions at 1720 cm-1 and at 2980 cm-1 on the IR spectrum. Propose a possible structure for this compound.

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Which of the following is true about CH3CH3+β€’?


A) it is the parent ion of ethane
B) it is a molecular ion of ethane with m/z = 30
C) it is a fragment of propane
D) it is a fragment of butane
E) A and B

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

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Which of the following wavenumber corresponds to the carbon/carbon triple bond region on an IR spectrum?


A) 1500 - 4000 cm-1
B) 400 - 4000 cm-1
C) 400 - 1500 cm-1
D) 2100 - 2300 cm-1
E) 1600 - 1850 cm-1

F) B) and D)
G) B) and C)

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High-resolution mass spectrometry is used to determine the _____ of a compound.


A) degree of unsaturation
B) molecular formula
C) molecular weight
D) B and C
E) none of these

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

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The separation of ions in the mass spectrometer is done by their ______.


A) electrons to protons ratio
B) mass to neutrons ratio
C) protons to neutrons ratio
D) mass to charge ratio
E) protons to electrons ratio

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

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Propose all possible structures for a compound with molecular formula C4H9N that shows two medium absorptions at 3400 cm-1 and no absorption in the range of 1600 - 1800 cm-1 in its IR spectrum.

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Which of the following compounds will have absorptions at 1700 cm-1 and 1320 cm-1? Which of the following compounds will have absorptions at 1700 cm<sup>-1</sup> and 1320 cm<sup>-1</sup>?   A)  I B)  II C)  III D)  IV E)  V


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

F) A) and E)
G) A) and D)

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Which one of the following compounds is consistent with the following IR spectrum? Which one of the following compounds is consistent with the following IR spectrum?   SDBS: National Institute of Advanced Industrial Science and Technology   A)  I B)  II C)  III D)  IV E)  V SDBS: National Institute of Advanced Industrial Science and Technology Which one of the following compounds is consistent with the following IR spectrum?   SDBS: National Institute of Advanced Industrial Science and Technology   A)  I B)  II C)  III D)  IV E)  V


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

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

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Propose a possible structure for a compound with molecular formula C6H5Br.

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blured image_TB4454_00...

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How will you distinguish between the following compounds using high-resolution mass spectrometry? How will you distinguish between the following compounds using high-resolution mass spectrometry?

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Compound I: m/z at 1...

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GC-mass spectrometry is used to find the _________ of each compound in a __________.


A) molecular formula, mixture of alkanes
B) molecular weight, mixture of compounds
C) molecular formula, mixture of compounds
D) B and C
E) none of these

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

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Which of the following is currently most often used to indicate the location of a signal on an IR spectrum?


A) wavelength
B) wavenumber
C) frequency
D) A and B
E) all of these

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

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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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CH3CH2CH2C≑CCH2CH2CH3
Absorptions fo...

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Diluted alcohols show a _____absorption around 3600 cm-1, due to _____.


A) sharp, hydrogen bonding
B) broad, hydrogen bonding
C) sharp, absence of hydrogen bonding
D) broad, absence of hydrogen bonding

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

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Arrange the following electromagnetic radiation in decreasing (highest to lowest) order of wavelength. Arrange the following electromagnetic radiation in decreasing (highest to lowest)  order of wavelength.   A)  V > III > IV > II > I B)  II > V > III > IV > I C)  I > IV > III > V > II D)  V > II > IV > III > I E)  II > IV > V > III > I


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

F) C) and E)
G) A) and C)

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