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Chromotagraphy exam qs

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Total cards: 13•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

State how the amino acids can be made visible at the end of the experiment.

Back (Answer)

use uv lamp or ninhydrin

#2
Front (Question)

State why each amino acid has a different Rf value

Back (Answer)

no balance between solubility in moving phase and retention in stationary phase

#3
Front (Question)

Suggest a suitable reagent for the hydrolysis of a protein.

Back (Answer)

Conc HCl

#4
Front (Question)

Suggest how the positions of the amino acids on the TLC plate were located

Back (Answer)

ultraviolet light

#5
Front (Question)

Suggest why it was necessary to use two different solvents

Back (Answer)

Some amino acids have the same Rf value

#6
Front (Question)

Outline the steps needed to locate the positions of the amino acids on the TLC plate and to determine their Rf values.

Back (Answer)

Outline the steps needed to locate the positions of the amino acids on the TLC plate and to determine their Rf values.

#7
Front (Question)

Explain why different amino acids have different Rf values. 2 marks

Back (Answer)

Amino acids have different polarities 1 Therefore, have different retention on the stationary phase or different solubility in the developing solvent

#8
Front (Question)

To obtain the chromatogram, the TLC plate was held by the edges and placed in the solvent in the beaker in the fume cupboard. The lid was then replaced on the beaker. Give one other practical requirement when placing the plate in the beaker

Back (Answer)

Solvent depth must be below start line

#9
Front (Question)

A third TLC experiment was carried out using 1,2‑dinitrobenzene. An identical plate to that in part (c) was used under the same conditions, but the solvent used contained a mixture of hexane and ethyl ethanoate. A student stated that the Rf value of 1,2‑dinitrobenzene in this third experiment would be greater than that of 1,2‑dinitrobenzene in the experiment in part (f) Is the student correct? Justify your answer.

Back (Answer)

Solvent (more) polar or ethyl ethanoate is polar Polar isomer more attracted to

#10
Front (Question)

Describe a test-tube reaction, on the product, to show that the cyclohexanol had been dehydrated. State what you would observ

Back (Answer)

addbromine water decoluaries

#11
Front (Question)

Explain why it is important to open the tap of the separating funnel periodically.

Back (Answer)

avoid pressure build-up

#12
Front (Question)

Give a property of anhydrous calcium chloride, other than its ability to absorb water, that makes it suitable as a drying agent in this preparatio

Back (Answer)

inert

#13
Front (Question)

Explain why cyclohexene has a shorter retention time than cyclohexanol.

Back (Answer)

less polar than cyclohexano Cyclohexene has a greater affinity/attraction for the mobile phase/hexane / cyclohexanol has a greater affinity/attraction for the stationary phase/silica