A) affinity chromatography
B) ion-suppression chromatography
C) ion-pair chromatography
D) gel-permeation chromatography
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Multiple Choice
A) carrier gas flow rate
B) column temperature
C) injection volume
D) analyte polarity
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Multiple Choice
A) for the removal of extraneous ions that produce complicating peaks in the mass spectrum
B) for quantification utilizing an internal standard
C) for confirmation of results obtained by electron-ionization mass spectrometry alone
D) for quality control checks on the mass spectrometry procedure
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Multiple Choice
A) the ion of highest relative abundance in the spectrum
B) the ion from which all other fragment ions are derived
C) always observed in the mass spectrum
D) all of the above
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Multiple Choice
A) 22.5%, 100%
B) 250%, 100%
C) 100%, 22.5%
D) 100%, 40%
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Multiple Choice
A) the carrier gas
B) the injector port
C) the column
D) the detector
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Multiple Choice
A) 1 and 4 are correct for normal-phase chromatography
B) 2 and 3 are correct for normal-phase chromatography
C) 1 and 3 are correct for reversed-phase chromatography
D) 2 and 4 are correct for reversed-phase chromatography
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Multiple Choice
A) absorbance, fluorescence, electrochemical
B) fluorescence, absorbance, electrochemical
C) electrochemical, fluorescence, absorbance
D) absorbance, electrochemical, fluorescence
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Multiple Choice
A) Consider analysis of these compounds by liquid chromatography.
B) Consider analysis of these compounds by gas chromatography at significantly elevated temperatures.
C) Consider chemical derivatization of these compounds prior to gas chromatography.
D) Report that these compounds cannot be analyzed by gas chromatography because of the lack of volatility.
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Multiple Choice
A) thermal-conductivity detector
B) flame-ionization detector
C) electron-capture detector
D) mass-spectrometer detector
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Multiple Choice
A) chromatographic analysis in which the mobile phase composition constantly changes during the chromatographic analysis
B) chromatographic analysis in which the mobile phase composition remains constant during the chromatographic analysis
C) chromatographic analysis in which the temperature of the stationary phase constantly changes during the chromatographic analysis
D) chromatographic analysis in which the temperature of the stationary phase remains constant during the chromatographic analysis
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Multiple Choice
A) thermal-conductivity detector
B) flame-ionization detector
C) nitrogen-phosphorus detector
D) electron-capture detector
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Multiple Choice
A) CI, EI, CI
B) CI, EI, EI
C) EI, CI, CI
D) EI, CI, EI
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Multiple Choice
A) to help dissolve the basic compounds in the mobile phase
B) to adjust the pH of the mobile phase to the desired basic pH
C) to block free silanol sites on the stationary phase from reacting with the basic solutes
D) to establish a flat baseline for spectrophotometric measurements
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Multiple Choice
A) It compensates for loss during sample preparation, injection imprecision, and detector variation.
B) It allows for analyte quantification.
C) It serves as a quality-control check.
D) All of the above
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Multiple Choice
A) It must be chemically and chromatographically inert.
B) It must be pure and dry.
C) It must be matched with the appropriate gas-chromatographic detector.
D) All of the above
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Multiple Choice
A) adsorption chromatography
B) partition chromatography
C) ion-exchange chromatography
D) gel-permeation chromatography
Correct Answer
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Multiple Choice
A) adsorption chromatography
B) partition chromatography
C) ion-exchange chromatography
D) gel-permeation chromatography
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Multiple Choice
A) These detectors will provide semi-quantitative data only.
B) These detectors will provide preliminary solute identification only.
C) These detectors will not provide a linear relationship between detector output (e.g., absorbance) and concentration.
D) These detectors lack the needed sensitivity to be useful in clinical laboratory analysis.
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Multiple Choice
A) use of a chiral stationary phase specifically designed for the enantiomeric pair
B) use of a mobile phase containing a chiral complexing agent which forms diastereomeric complexes during the chromatographic analysis
C) chemical derivatization of the enantiomeric pair, forming diastereomers prior to chromatographic analysis
D) chemical derivatization of the enantiomeric pair, forming diastereomers following chromatographic analysis
Correct Answer
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