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Topic 2 Bonding & Structure

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

Ice & I2 have open lattice structures. What is that?

Back (Answer)

Simple molecules held together in a lattice by intermolecular forces of attraction.

#2
Front (Question)

Ionic bonding

Back (Answer)

Strong electrostatic attraction between oppositely-charged ions held in a giant lattice.

#3
Front (Question)

Why do ionic radii decrease down a group?

Back (Answer)

More shells of electrons.

#4
Front (Question)

What experiment can be used to show a compound is ionic?

Back (Answer)

Electrodes in a circuit are placed in a solution of the ionic compound. The bulb lights up.

#5
Front (Question)

Isoelectronic

Back (Answer)

Ions with the same electron configuration as a Noble gas.

#6
Front (Question)

What is the trend in bond strength/enthalpy and bond length down group 7?

Back (Answer)

Bond lengths increases and bond strength/enthalpy decreases. Exception: F-F, which has the shortest bond length yet the lowest bond enthalpy.

#7
Front (Question)

Why is F-F an exception to the bond length & strength trend down group 7?

Back (Answer)

The lone pairs around each F atom repel, which weakens the covalent bond.

#8
Front (Question)

Covalent bond

Back (Answer)

Strong electrostatic attraction between 2 nuclei and the shared pair of electrons between them.

#9
Front (Question)

Sigma bond

Back (Answer)

Covalent bond where the p-orbitals overlap end-to-end.

#10
Front (Question)

Pi bond

Back (Answer)

Covalent bond that forms only after a sigma bond has formed, usually by the sideways overlap of p-orbitals.

#11
Front (Question)

Dative/coordinate covalent bond

Back (Answer)

Formed when one atom donates both bonding electrons.

#12
Front (Question)

Bond length

Back (Answer)

Sum of the atomic radii.

#13
Front (Question)

What determines the strength of a covalent bond?

Back (Answer)

Bond length. Longer bonds are weaker, hence the hydrolysis of the C-X bond in halogenoalkanes.

#14
Front (Question)

P & S in period 3

Back (Answer)

Can hold more than 8 e- in the outer shell due to the availability of energetically favourable orbitals.

#15
Front (Question)

Describe the bonding in graphene.

Back (Answer)

Same as in graphite. Single layer of hexagonal rings. Delocalised e- are free to move to conduct electricity.

#16
Front (Question)

Describe the bonding in graphite.

Back (Answer)

Each C has 3 sigma bonds & 1 delocalised e-. Planar hexagonal rings held together by London forces. Layers can slide over each other, and e- are free to move to conduct electricity.

#17
Front (Question)

Where can the delocalised e- move in graphite?

Back (Answer)

Electrons flow parallel to the layers. The energy gap is too big to allow perpendicular flow.

#18
Front (Question)

Describe the bonding in diamond.

Back (Answer)

Each C forms 4 sigma bonds. Tetrahedral. Numerous, strong covalent bonds.

#19
Front (Question)

Explain why some ionic compounds have higher melting points than others.

Back (Answer)

Compare charge and ionic radius. Higher charge density of the cation = greater attraction between the cation & anion.

#20
Front (Question)

Migration of ions experiment

Back (Answer)

Electrolysis of a green copper (II) chromate (VI) solution. Cu2+ ions migrate to the cathode and appear yellow. Chromate ions migration to the anode and appear blue.

#21
Front (Question)

In a negative ion, which atom gains the e-?

Back (Answer)

The more electronegative one.

#22
Front (Question)

Why do alcohols have higher boiling points than alkanes of the same chain length?

Back (Answer)

Alcohols have hydrogen bonding, but alkanes have only London forces.

#23
Front (Question)

Why does HF have hydrogen bonding but HBr does not?

Back (Answer)

F is small & electronegative, so creates a greater dipole moment in HF, meaning it can attract the lone pair on the F of another molecule.

#24
Front (Question)

Why do branched isomers have lower boiling points than straight-chain isomers?

Back (Answer)

Branched molecules have fewer points of contact, so weaker London forces.