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What else can I help you with?
What is an eluent?
An eluent is a solvent or liquid used in chromatography to carry the sample through the stationary phase, enabling the separation of the components based on their chemical properties. It is important for the eluent to be compatible with the stationary phase and the sample being analyzed to achieve efficient separation.
What happens if the eluent is above the 1.5cm line in a chromatography experiment?
If the eluent is above the 1.5cm line in a chromatography experiment there will not be a proper distribution in a test tube to discover the sources of ink on a paper. A chromatography experiment tests for the sources of ink whether it be chemical or plant based.
What is the difference between the stationary phase and the mobile phase in chromatography?
stationary phase stays at the bottom of the paper chromatography while mobile phase is moving on the stationary phase and move on stationary phase till it gets its right place on the top of the paper or somwhere else.
What problem will ensue if the level of the developing liquid is higher than the applied spot in a TLC analysis?
The effect on chromatographic work if the solvent level in the developing chamber is higher than the spotted sample is a thin layer chromatography. The solvent becomes polar enough and spot will move some distance.
What would have been the result if a large quantity of petroleum ether alone were used as the eluent in either of the experiments described in column chromatography?
petroleum ether is a lot less polar than solvents like MTBE and the hexanes. so if the stationary phase is a lot more polar than the solvent then the components of the mixture that were added to the column to be separated will get stuck in the stationary phase
What is an eluent?
An eluent is a solvent or liquid used in chromatography to carry the sample through the stationary phase, enabling the separation of the components based on their chemical properties. It is important for the eluent to be compatible with the stationary phase and the sample being analyzed to achieve efficient separation.
What is eluent front?
Oh, dude, the eluent front is like the cool kid at the chromatography party. It's basically the furthest point reached by the solvent in a chromatography experiment. So, if you're ever lost in the world of chromatography, just look for the eluent front and follow it like a trail of breadcrumbs... or in this case, a trail of solvent.
What are three way that mixtures can separated?
Three ways would be Liquid liquid - distillation (separation based on boiling points) Column chromatography separates solids dissolved in eluent based on polarity Filtration (washing with a solvent that dissolves one compound and not another)
What is the advantage of allowing the eluent front to rise near the top of the TLC sheet rather than stopping when only half way up?
When you calculate RF values, you need the distance moved by the dye (or whatever you're using) and the distance moved by the solvent (the eluent front) Given that no matter where the eluent front stops your measurement will always have the same standard error (say +- 1mm if you're using TLC plates and a normal ruler), then the further your eluent front and dye move, the less that measurement error will impact on your RF value - the error will be a smaller % of the overall distance.
Eluent front distance from the origin for blue dye?
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What happens if the eluent is above the 1.5cm line in a chromatography experiment?
If the eluent is above the 1.5cm line in a chromatography experiment there will not be a proper distribution in a test tube to discover the sources of ink on a paper. A chromatography experiment tests for the sources of ink whether it be chemical or plant based.
What is the difference between the stationary phase and the mobile phase in chromatography?
stationary phase stays at the bottom of the paper chromatography while mobile phase is moving on the stationary phase and move on stationary phase till it gets its right place on the top of the paper or somwhere else.
What is the function of suppressor column in HPLC?
As far as I'm aware, suppressor columns are primarily used in ion chromatography just. They remove strong ions (ie replace Na+ with H+) allowing for a decrease in background detection (due to the eluent). A link is provided to the process that goes on in a suppressor for IC made by metrohm
What is the retardation factor?
In chemical chromatography, it is a measure of the relative mobility of components of a mixture through a stationary phase while experiencing the forces of a mobile eluent phase, based on relative intermolecular attractive forces and molecular size. In thin layer chromatography, is it the ratio of distance travelled by a component compared to the distance travelled by the eluent front from the point of contact with the mixture. In column chromatography, it is the fraction of the component in the mobile phase at equilibrium. By comparison, in gas chromatography, relative retention times on the stationary phase are measured and compared for the mixture components.
What problem will ensue if the level of the developing liquid is higher than the applied spot in a TLC analysis?
The effect on chromatographic work if the solvent level in the developing chamber is higher than the spotted sample is a thin layer chromatography. The solvent becomes polar enough and spot will move some distance.
What would have been the result if a large quantity of petroleum ether alone were used as the eluent in either of the experiments described in column chromatography?
petroleum ether is a lot less polar than solvents like MTBE and the hexanes. so if the stationary phase is a lot more polar than the solvent then the components of the mixture that were added to the column to be separated will get stuck in the stationary phase
Is benzene and chloroform mixture a good eluent?
A good eluent is one that gives good separation between your target compound and impurities. Use a TLC plate to get a feel for the effect of the eluent on your purification. If this is your first time purifying this reaction, a good Rf to aim for in regard to your target compound is 0.2 - 0.25, and impurities should have at least an Rf difference of 0.1 - 0.15 compared to your target compound. Benzene is rather toxic and should not be used for eluting large quantities of compound. But if your reaction is around 2g scale or less, benzene should be ok.
