2.3 The metallic model
- Syllabus
- First assessment 2025
- Topic
- 2.3
- Level
- SL
Metallic bonding is the electrostatic attraction between a lattice of positive metal ions and delocalized electrons.


Delocalized electrons can move through the structure and carry charge and thermal energy. Non-directional attraction allows layers of cations to slide while the bonding remains.
When a potential difference is applied, delocalized electrons drift through the fixed cation lattice and carry charge; the positive ions do not travel through the metal. When layers shift under force, non-directional attraction to the electron sea persists, explaining malleability rather than brittle fracture.
Property-to-use link: copper is used for electrical wiring because its delocalized electrons carry charge through the solid; aluminium can be rolled into foil because ion layers can shift while non-directional metallic attraction is maintained. A use must be justified by the relevant property, not merely by stating that the substance is a metal.
3 marks
Describe metallic bonding and how it contributes to electrical conductivity.
Metallic-bond strength depends on the attraction between metal ions and delocalized electrons. Ion charge, ion radius, and the number of delocalized electrons affect charge density and attraction.
A larger ion radius generally lowers attraction; greater charge or more delocalized electrons can strengthen metallic bonding. Use the stated comparison rather than a memorized trend alone.
Compare Na and Mg using the model: Mg supplies more delocalized electrons and forms smaller, more highly charged ions, giving stronger attraction and a higher melting point. State all relevant factors before predicting; across broader sets, lattice structure can prevent a perfectly smooth trend.
2 marks
Explain why the melting points of the group 1 metals (Li→Cs) decrease down the group.
Retrieve the model: positive ions attract delocalized electrons; electron mobility explains conductivity and non-directional bonding explains malleability; charge, radius, and d-electron contribution explain strength trends.
A complete property explanation should name the cation lattice, delocalized electrons, and the specific structural change relevant to the property.