Thin-Layer Chromatography (Cambridge (CIE) A Level Chemistry): Exam Questions

A student sets up a thin-layer chromatography experiment.

Explain why:

i) the baseline is drawn in pencil rather than ink.

[1]

ii) a lid is placed on the container during the experiment.

[1]

A student runs a thin-layer chromatography experiment and plans to determine the compounds from their R_f values.

Describe the steps that the student needs to perform to determine the identity of the compounds. 

The compounds in the mixture are colourless.

Suggest how the student could locate the spots on the TLC plate.

The student runs another TLC practical on a mixture of benzaldehyde and benzyl alcohol using 7:3 pentane / diethyl ether as a solvent.

The student's chromatogram is shown in Fig. 1.1.

Fig. 1.1

Calculate the R_f values for both compounds in the chromatogram. Show your working.

Explain why the maximum R_f value of a compound cannot exceed 1.

Thin layer chromatography was used to analyse the contents of a bottle containing butan-2-ol and butanone. 

The contents of the bottle were dissolved in hexane and spotted onto the silica plate. 

Explain why butanone has a higher R_f value than butan-2-ol.

State the names of the stationary and mobile phases in this chromatography experiment.

The student repeats the experiment using a more polar solvent instead of 7:3 pentane / diethyl ether.

Suggest and explain the effect on the R_f value of benzyl alcohol.

Thin-layer chromatography (TLC) is used to analyse samples of organic compounds.

Fig. 3.1 shows the structure of ibuprofen.

Fig. 3.1

Calculate the M_r of ibuprofen to 1 decimal place.

State two advantages of using TLC for the analysis of organic samples.

Thin-layer chromatography was performed on a sample of ibuprofen.

Only one spot was expected on the TLC plate but two were observed.

Suggest why the ibuprofen sample produced two spots on the TLC plate rather than one.

Dinitrobenzene has the molecular formula C₆H₄N₂O₄.

i) Draw the skeletal formulae of the three structural isomers of dinitrobenzene.

[3]

ii) State the type of structural isomerism shown.

[1]

State the factors that determine the distance travelled by a spot in thin-layer chromatography.

Samples of 1,2-dinitrobenzene and 1,4-dinitrobenzene are spotted on a thin-layer chromatography plate coated with silica gel.

The solvent used to run the thin-layer chromatography experiment is hexane.

Suggest why each sample is applied to the thin-layer chromatography plate using a fine capillary tube rather than a dropping pipette.

Fig. 1.1 shows the chromatogram with the spot for 1,4-dinitrobenzene.

Fig. 1.1

Draw the expected position of the spot for 1,2-dinitrobenzene. Explain your answer.

Explain what the student could do to reverse the relative positions of the 1,2-dinitrobenzene and 1,4-dinitrobenzene spots.