Reactions of Aqua Ions
Metal ions in water exist as hexaaqua ions [M(H₂O)₆]ⁿ⁺. 3+ ions are more acidic than 2+: higher charge density polarises the O–H bonds in water ligands, releasing H⁺. With OH⁻ or a little NH₃, ions are deprotonated to neutral hydroxide precipitates: Cu²⁺ blue; Fe²⁺ green (turns brown in air); Fe³⁺ orange-brown; Cr³⁺ grey-green; Al³⁺ white; Mn²⁺ off-white (browns). Excess NaOH dissolves amphoteric Al(OH)₃ and Cr(OH)₃. Excess NH₃ causes ligand exchange: Cu²⁺ gives deep blue ; Cr³⁺ gives purple . With carbonate, 2+ ions give MCO₃ precipitates; 3+ ions are acidic enough to give the hydroxide + CO₂.
Learning objectives
- Explain why 3+ aqua ions are more acidic.
- Describe precipitates with NaOH and NH₃ and their colours.
- Describe reactions with excess reagents and with carbonate.
- Identify ions from observations.
Why does Fe³⁺(aq) fizz with sodium carbonate, while Fe²⁺(aq) just gives a precipitate?
Core idea
Drip sodium hydroxide into metal ion solutions and you get a rainbow of precipitates. Each colour is a fingerprint.
Aqua ions lose H⁺ from water ligands. Lose enough to become neutral and a precipitate forms; 3+ ions lose H⁺ more readily, so they're more acidic.
1. Deprotonation
- Hexaaqua ion.
- One H⁺ removed by OH⁻.
- Three removed: neutral, insoluble, orange-brown.
Watch the colour and whether excess dissolves it.
Na₂CO₃ is added to Al³⁺(aq) and to Cu²⁺(aq). Predict observations.
- Goal
- Observations.
- Strategy
- Compare acidity of 3+ and 2+ ions.
- Acidic enough to release CO₂; Al(OH)₃ forms.
- CuCO₃ precipitates.
Summary
- 3+ aqua ions more acidic.
- Neutral complex = precipitate.
- Al, Cr amphoteric.
- Excess NH₃ ligand exchange.
- Amphoteric
- Reacts with both acids and bases.
- Deprotonation
- Loss of H⁺.
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