True or false
The Van Deemter equation applies to both packed and open tubular columns.
→ FalseThe retention time is the time taken for a solute to elute from the column.
→ TrueHPLC uses a gaseous mobile phase.
→ FalseThe magnetic sector analyzer separates ions based on charge only.
→ FalseIn GC, the stationary phase is always liquid.
→ FalseTime-of-flight analyzers offer high resolution.
→ FalseMolecular mass spectrometry requires less energetic ion sources than atomic mass spectrometry.
→ TrueElectrospray ionization is commonly used for molecular MS.
→ TrueMass spectrometry always destroys the sample.
→ FalseA chromatogram plots signal vs. time.
→ TrueIncreasing column length increases resolution.
→ TrueThe retention factor can never be negative.
→ TrueThe selectivity factor must always be greater than 1.
→ TrueBand broadening is desirable in chromatography.
→ FalseThe mobile phase in reversed-phase HPLC is polar.
→ TrueIncreasing flow rate decreases longitudinal diffusion.
→ TrueIon-exchange chromatography is suitable for separating neutral molecules.
→ FalseIn TOF mass analyzers, ions are separated based on kinetic energy.
→ FalseGC/MS can analyze thermally unstable compounds.
→ FalseDetectors in HPLC should have low internal volume.
→ TrueMass spectrometry can measure isotopic patterns.
→ TrueThe mass spectrum is specific to each compound.
→ TrueHPLC requires very high pressure for the mobile phase.
→ TrueAnalytes with lower k values elute first.
→ TrueSolvent polarity affects retention in HPLC.
→ TrueThe stationary phase in size-exclusion chromatography is inert.
→ TrueMS resolution improves with higher Δm.
→ FalseCapillary columns offer better separation than packed columns in GC.
→ TrueSelectivity factor equals 1 when two solutes are perfectly separated.
→ FalseA detector's response must always be linear.
→ FalseThe van Deemter equation includes longitudinal diffusion.
→ TrueSolute diffusion rate does not affect peak width.
→ FalseHPLC can be applied to proteins.
→ TrueSample loss is minimal in direct probe inlets.
→ FalseThe number of theoretical plates is a measure of column efficiency.
→ TrueTOF analyzers have limited mass range.
→ FalseGC/MS is destructive analysis.
→ TrueMS detectors do not require a vacuum.
→ FalseIon source type affects fragmentation pattern.
→ TrueResolution increases as peak widths decrease.
→ TrueIncreasing temperature always improves GC separation.
→ FalseRetention time is influenced by column temperature.
→ TrueAll analytes have the same retention factor under same conditions.
→ FalseHPLC detectors can include mass spectrometers.
→ TrueElectrochemical detectors can be used in HPLC.
→ TrueRefractive index detectors are suitable for gradient elution.
→ FalseColumn efficiency is independent of flow rate.
→ FalseThe detector in MS counts the number of ions.
→ TrueThe resolution of a column can be computed using peak widths.
→ TrueIon trap MS allows storage and scanning of ions.
→ True
✅ 10 ENUMERATION ITEMS (Parts/Filling)
Enumerate the main components of a mass spectrometer.
→ Ion source, mass analyzer, detector, vacuum systemEnumerate the steps in mass spectrometry analysis.
→ Ionization, mass separation, detection, data analysisEnumerate 3 types of mass analyzers.
→ Quadrupole, magnetic sector, TOFEnumerate 3 common ion sources in molecular MS.
→ Electrospray ionization, MALDI, electron impactEnumerate the detectors used in HPLC.
→ UV, IR, fluorescence, refractive index, electrochemicalEnumerate 3 types of HPLC based on mechanism.
→ Normal-phase, reversed-phase, size-exclusionEnumerate the axes in a chromatogram.
→ X-axis: retention time; Y-axis: detector signalEnumerate the parameters in the Van Deemter equation.
→ A (multiple path), B (longitudinal diffusion), C (mass transfer), u (flow rate)Enumerate at least 2 applications of HPLC.
→ Pharmaceutical analysis, food additive detectionEnumerate 3 outputs from a mass spectrum.
→ m/z value, peak height, relative abundance