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Carbonyl Compounds

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Total cards: 6•Content version: v3•Public deck•Updated: 8/1/2026

Card preview (6)

#1
Front (Question)

Use of methanal

Back (Answer)

Was used by biologists to preserve specimens but now restricted due to toxicity. Still raw material for the manufacture for a range of thermosetting plastics.

#2
Front (Question)

Use of propanone

Back (Answer)

Common solvent and used as nail polish remover

#3
Front (Question)

Intermolecular forces in carbonyl compounds

Back (Answer)

London forces and dipole-dipole interactions

#4
Front (Question)

Why is hydrogen bonding possible with water

Back (Answer)

Between carbonyl group and OH of water due to long pair of oxygen atom

#5
Front (Question)

Why are bps of carbonyl compounds lower than alcohols of same size

Back (Answer)

As cannot form hydrogen bonds between molecules

#6
Front (Question)

Why do longer chain carbonyl compounds not dissolve in water

Back (Answer)

As carbon chain lengthens London forces stronger and energy to overcome London forces becomes stronger than energy released in hydrogen bonding with water meaning cannot disrupt hydrogen bonding network/ overcome London forces between chains