Metal ions become hydrated in water (H2O ligands around a central ion) and they form coloured precipitates that can be used to identify the metal ion present.
When ions are in solution they are acidic, 3+ ions are more acidic than 2+ because they dissociate more so have a greater attractive power to OH-.
Metal ions in solution react as acids with NaOH in a neutralisation reaction to form a salt and water.
Aluminium salt can act as an acid or a base meaning it is amphoteric.
Metal ions react with aqueous ammonia to form a salt and ammonium ions.
Solutions of these metal 2+ ions react with sodium carbonate as acids forming insoluble carbonates and water.
Solutions of metal 3+ ions act as stronger acids so they react with sodium carbonate to form a salt, water and carbon dioxide.
All metal aqua ions undergo ligand substitution when reacted with chlorine ions to form tetrahedral ions with four chlorine ligands (occurs when they react with concentrated HCl).
3+ ions form stronger acids as they have a larger charge density so are more polarising and can break O-H bonds more easily.
Sodium and magnesium oxide form alkaline solutions because they react with water to produce hydroxide ions. However, sodium hydroxide is more soluble than magnesium hydroxide (dissociates more).
In the contact process, vanadium oxide is used as a catalyst to convert sulfur dioxide to sulfur trioxide.
Complexes formed from transition metal ions are coloured because they absorb some wavelengths of visible light which excites the electrons in the d-orbitals so the remaining wavelengths of light are transmitted to give out colour.