why do we use organic mobile phase and aqueous mobile phase together in LC MS
LCMS essentially means Liquid Chromatography Mass Spectroscopy. Usually in Liquid chromatography, there will be only one mobile phase, which will be a liquid. It is used to separate a solution. But in LCMS, it is used to separate then it is analyzed in mass spectroscopy. So inorder to obtain the molecule in the mass spectrometer, it is essential to move the separated molecules to the mass spectrometer. If we use only organic mobile phase, only substances which interacts with organic phase will be separated and moved to mass spectrometer. Then we use aqueous mobile phase to take the remaining substances to the mass spectrometer for analysis.
why do we use organic mobile phase and aqueous mobile phase together in LC MS
Why would it be unwise to use 100% ethyl acetate as the first mobile phase you test when determining the best mobile phase to separate the mixture of analgesics in Procedure? Why do polar compounds move slower up the silica TLC plates than nonpolar compounds? Why does increasing the polarity of the mobile phase increase the rate at which all compounds move up the plate?
Draw a diagram of the components of a QTrap LC MS/MS. (We used ABSciex Qtrap 2000 LC/MS/MS with an Agilent 1200LC as an example)
(a) In what order do you expect the following species to be eluted in normal-phase LC? Indicate with numbers and provide brief rationale: 0₂N NO₂ NO2 trinitrotoluene 1-heptene heptane heptane phenol toluene (b) Fraction of which component of the mobile phase should be increased when a hexane/acetone gradient is employed to facilitate elution of phenol and trinitrotoluene? Provide brief rationale
(a) In what order do you expect the following species to be eluted in normal-phase LC? Indicate with numbers and provide brief rationale: 0₂N NO₂ NO2 trinitrotoluene 1-heptene heptane heptane phenol toluene (b) Fraction of which component of the mobile phase should be increased when a hexane/acetone gradient is employed to facilitate elution of phenol and trinitrotoluene? Provide brief rationale
Using a nonpolar stationary phase and a mobile phase consisting of a 50:50 mixture of aqueous acetic acid and methanol, rank the following compounds in order of elution off of a HPLC column: Acetaminophen, caffeine, aspirin and benzoic acid
Why was it important to filter and degas the mobile phase and the samples? How is the “reversed-phase” HPLC used here different from “normal-phase” with regard to stationary and mobile phases, and order of elution? Mobile Phase Composition (a) If the mobile phase composition was changed from 65:35:1 (v/v/v) to 75:25:1 (v/v/v) water:methanol:acetic acid, how would the time of elution (expressed as retention time) for caffeine be changed, and why would it be changed? (b) What if it was changed...
Why was it important to filter and degas the mobile phase and the samples? How is the “reversed-phase” HPLC used here different from “normal-phase” with regard to stationary and mobile phases, and order of elution? Mobile Phase Composition (a) If the mobile phase composition was changed from 65:35:1 (v/v/v) to 75:25:1 (v/v/v) water:methanol:acetic acid, how would the time of elution (expressed as retention time) for caffeine be changed, and why would it be changed? (b) What if it was changed...
why do we add an when naming organic compounds. example is why do we write methanal and not methal
From Mcmurry's organic chemistry 9th edition chapter 18, problem 3p --> (c) why do we use isopropanol with benzyl bromide instead of isopropyl bromide and benzyl alcohol?
For a nonpolar solute, why does the mobile phase strength increase as the solvent becomes less polar in reversed-phase chromatography?