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F324 Past Papers

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Total cards: 23•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (23)

#1
Front (Question)

What happens wen something reacts with tollens?

Back (Answer)

It is oxidised.

#2
Front (Question)

When bromine reacts with phenol what would you observe to happen?

Back (Answer)

A white precipitate forms, And bromine decolourise.

#3
Front (Question)

What are problems with kukele?

Back (Answer)

Enthalpy change of hydrogenation is less exothermic than expected.

#4
Front (Question)

What is retention time?

Back (Answer)

The time from the injection of a sample for the component to leave the column.

#5
Front (Question)

What are problems with chiral drugs?

Back (Answer)

Production or separation of a single isomer can be difficult. Another isomer may be harmful.

#6
Front (Question)

How can problems with chiral drugs be overcome?

Back (Answer)

Enzymes. Chiral synthesis.

#7
Front (Question)

How can you derive the structure of a compound through the Bradys test?

Back (Answer)

Take the melting point of product and compare with known values.

#8
Front (Question)

When do you leave the ends?

Back (Answer)

When asked for repeats.

#9
Front (Question)

How does a liquid stationary phase separate compounds in a mixture?

Back (Answer)

Relative solubility

#10
Front (Question)

What are problems with kukele?

Back (Answer)

Enthalpy change of hydrogenation is less exothermic than expected.

#11
Front (Question)

What is retention time?

Back (Answer)

The time from the injection of a sample for the component to leave the column.

#12
Front (Question)

What are problems with chiral drugs?

Back (Answer)

Production or separation of a single isomer can be difficult. Another isomer may be harmful.

#13
Front (Question)

How can problems with chiral drugs be overcome?

Back (Answer)

Enzymes. Chiral synthesis.

#14
Front (Question)

How can you derive the structure of a compound through the Bradys test?

Back (Answer)

Take the melting point of product and compare with known values.

#15
Front (Question)

When do you leave the ends?

Back (Answer)

When asked for repeats.

#16
Front (Question)

How does a liquid stationary phase separate compounds in a mixture?

Back (Answer)

Relative solubility

#17
Front (Question)

Why does the nitration of benzene make numerous products?

Back (Answer)

Substitution of NO2 at different points of the ring.

#18
Front (Question)

Write the formula of the salts formed when C2H5NH2 reacts with: Sulphuric acid Ethanoic acid

Back (Answer)

(C2H5NH3+)2 SO42– C2H5NH3+ CH3COO–

#19
Front (Question)

What is condensation polymerisation?

Back (Answer)

Monomers joining to form a chain and another small molecule like H2O.

#20
Front (Question)

What increases water solubility?

Back (Answer)

Forming more H bonds

#21
Front (Question)

What is the observation made when something is oxidised by K2Cr207?

Back (Answer)

Turns green or blue

#22
Front (Question)

What does the D2O shake show?

Back (Answer)

It removes an OH or NH peak

#23
Front (Question)

Explain the relative resistance to bromination of benzene and an alkene.

Back (Answer)

Benzene has delocalised pi bonds. Alkene has localised pi bonds between 2 carbons. Benzene has a lower e density. Benzene polarises Br2 less.