3.3.16 Chromatography Flashcards

1
Q

what are the basic principles of all kinds of chromatography?

A

a family of separation techniques that depend on the principle that a mixture is separated if it is dissolved in a solvent and this mobile phase is passed over a solid (the stationary phase)

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2
Q

what is the mobile phase?

A

carries the soluble components of the mixture

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3
Q

what relationship between a sample and the mobile phase makes the sample move faster?

A

more soluble components/ components with more affinity to the solvent move faster

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4
Q

what does the stationary phase do?

A

holds back components of the mixture that are attracted to it

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5
Q

what is the relationship between a sample and the stationary phase that makes the sample move slower? what kind of bonding does this often involve?

A

more affinity for the stationary phase means that a component moves slower; often attracted by hydrogen bonding

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6
Q

how are substances separated by chromatography?

A

if suitable stationary/mobile phases are chosen, the balance between affinity for the mobile phase and affinity for the stationary phase is different for each component of the mixture
thus, they move at different rates and are separated over time

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7
Q

Why will different substances show different Rf values?

A

they are bonded differently and have different polarities - more polar bonds mean longer retention time or smaller Rf value, since hydrogen bonding/dipoles are attracted more strongly to the stationary phase

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8
Q

what does TLC stand for?

A

thin layer chromatography

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9
Q

what is the stationary phase in TLC?

A

plastic/glass/metal sheet or plate coated in silica (SiO2) or alumina (Al2O3)

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10
Q

what are the advantages of TLC over paper chromatography?

A

runs faster
smaller amounts of mixture can be separated
TLC plates are more robust than paper

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11
Q

how can you observe colourless spots after TLC?

A

UV light
spray with developing agent (e.g. ninhydrin turns amino acid spots from colourless to purple, so they can be seen) (heating needed with ninhydrin)

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12
Q

how do we calculate Rf value?

A

measure the distance from the initial line (that the mixture was spotted onto) to the solvent front, and the distance from the initial line to the spot
Calculate Rf using Rf = distance moved by spot/ distance moved by solvent front

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13
Q

what does Rf value stand for?

A

Retention factor; a measure of the rate of movement of a component through the chromatography apparatus; a ratio between the rate of movement of the solvent and that component

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14
Q

How could you confirm the identity of a substance from its Rf value?

A

compare your Rf value to accepted values Rf for that substance run in the same solvent and set-up; if they match, then identity is confirmed

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15
Q

what is column chromatography?

A

column packed with silica, alumina or resin has solvent run through it downwards

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16
Q

what is the stationary phase in column chromatography?

A

silica, alumina or resin packed into a column

17
Q

what is the mobile phase in column chromatography? what is it also known as?

A

solvent added at the top and runs down the column; called “eluent”

18
Q

what are the advantages of column chromatography?

A

more than one eluent can be used, leads to better separation
fairly large amounts can be separated and collected after separation

19
Q

what is the stationary phase in gas-liquid chromatography?

A

powder, coated with oil packed into a long, thin, capillary tube (100m long, 0.5mm diameter)
coiled and placed in an oven, the temperature of which can be varied

20
Q

what is the mobile phase in gas-liquid chromatography?

A

carrier gas, inert e.g. N2 or He

21
Q

What do you measure in gas-liquid chromatography?

A

retention time; different components of the mixture take different amounts of time to move through

22
Q

what are the advantages of GLC?

A

very sensitive; GC can detect minute traces of substances in foodstuffs, and link oil pollution on beaches to the specific tanker the oil came from

23
Q

what are GLC’s uses?

A

test athletes’ and horses’ blood and urine for drugs

24
Q

how can you use GC or GCMS to identify substances?

A

match gas chromatograph to that of a known substance under the same conditions; retention time should exactly match
substance’s identity can be confirmed by mass spectroscopy, NMR or infrared spectroscopy

25
Q

how does GCMS work?

A

Gas Chromatography is run; retention time is recorded, then mixture is run through a mass spectrometer
fragmentation pattern/molecular ion peak confirms identity

26
Q

will an alcohol or an aldehyde have a shortest retention time by column chromatography? why?

A

aldehyde has a shorter retention time
it has a less polar bond than an alcohol so it adsorbs less strongly to the stationary phase, so moves down the column at a quicker rate
force of attraction between stationary phase and aldehyde is less