Chapter in a nutshell: how elements split into metals / non-metals, how a metal's place in the activity series decides its reactions and how it is extracted, plus corrosion, the extraction of aluminium and common alloys.
1. Metals vs Non-metals — Definitions
- Metal: an element that forms positive ions (cations) by losing electrons → electropositive. e.g. Na − e⁻ → Na⁺, Mg − 2e⁻ → Mg²⁺, Al − 3e⁻ → Al³⁺.
- Non-metal: an element that forms negative ions (anions) by gaining electrons → electronegative. e.g. Cl + e⁻ → Cl⁻, O + 2e⁻ → O²⁻, N + 3e⁻ → N³⁻.
- Number of electrons lost/gained = valency. (Of 118 elements, only ~22 are non-metals. H is a non-metal that forms H⁺.)
2. Comparison of Metals and Non-metals
| Property | Metals | Non-metals |
|---|---|---|
| Valence electrons | 1–3 (lose → cation) | 5–7 (gain → anion) |
| Physical state | solids (except Hg, Ga) | solids, gases, one liquid (Br₂) |
| Lustre | lustrous (dull: Pb) | dull (lustrous: iodine, graphite) |
| Hardness | hard, strong (soft: Na, K) | soft/brittle (hardest: diamond) |
| M.P / B.P / density | high (low: Na, K, Hg, Ga) | low (high: C, B, Si) |
| Malleable / ductile | yes (except Zn, Hg) | no (except carbon fibre) |
| Conductivity | good (best: Ag, Cu) | poor (except graphite) |
| Nature of oxide | basic / amphoteric | acidic / neutral |
| In electrolysis | discharged at cathode | discharged at anode |
| Redox behaviour | reducing agents | oxidising agents (except C, H) |
3. Position in the Periodic Table
- Alkali metals (Group IA): Li, Na, K, Rb, Cs, Fr — 1 valence e⁻, valency 1.
- Alkaline-earth metals (Group IIA): Be, Mg, Ca, Sr, Ba, Ra — 2 valence e⁻, valency 2.
- Metals fill the left + middle; non-metals the right; a zig-zag line of metalloids (B, Si, Ge, As, Sb, Te) separates them. Only one non-metal — H — sits on the left.
4. Alkali Metals (IA) — key features
- Very reactive → never found free; stored under kerosene.
- Soft (cut with a knife), low M.P/B.P; ionic salts (except some Li salts).
- Reactivity increases down the group; strong reducing agents (low ionisation energy).
- Flame colours: Li crimson red, Na golden yellow, K lilac/pale violet.
- Action of water: 2M + 2H₂O → 2MOH + H₂↑
- Action of acid: 2M + 2HCl → 2MCl + H₂↑
5. Alkaline-Earth Metals (IIA) — key features
- Less reactive than alkali metals, harder, higher M.P; form +2 ions; basic oxides/hydroxides.
- Action of water: M + 2H₂O → M(OH)₂ + H₂↑
- Action of acid: M + H₂SO₄ → MSO₄ + H₂↑
- Flame colours: Ca brick red, Sr crimson, Ba apple green (Be, Mg give none).
6. Nature of Oxides
| Type | Examples |
|---|---|
| Basic | Na₂O, CaO, MgO, Fe₂O₃, CuO |
| Amphoteric (react with both acid & base) | Al₂O₃, ZnO, PbO |
| Acidic | CO₂, SO₃, NO₂, P₂O₅ |
| Neutral | CO, NO, N₂O, H₂O |
7. The Activity (Reactivity) Series
K Na Ca Mg Al Zn Fe Pb (H) Cu Hg Ag Au (most reactive / most electropositive / strongest reducing → least)- Electropositive character & reducing power decrease down the series.
- Action of water: K, Na react with cold water; Ca with cold water (no ignition); Mg with hot water/steam; Al, Zn, Fe only with steam (e.g. 3Fe + 4H₂O ⇌ Fe₃O₄ + 4H₂); Cu and below — no reaction.
- Action of dilute acid: metals above H displace hydrogen (e.g. Zn + 2HCl → ZnCl₂ + H₂); metals below H (Cu, Hg, Ag, Au) do not.
- Displacement: a higher metal displaces a lower one from its salt solution.
8. Reduction of Metal Oxides
- Oxides of K, Na, Ca, Mg, Al cannot be reduced by C, CO or H₂ → extracted by electrolysis.
- Oxides below Al (Zn, Fe, Pb, Cu) can be reduced by C / CO / H₂:
- Oxides of Hg, Ag decompose on heating alone (2HgO → 2Hg + O₂).
9. Action of Heat on Metallic Compounds
| Compound | K, Na | Ca, Mg, Al, Zn, Fe, Pb, Cu | Hg, Ag |
|---|---|---|---|
| Carbonates | stable (K, Na) | → oxide + CO₂ (e.g. ZnCO₃ → ZnO + CO₂) | → metal + CO₂ + O₂ |
| Hydroxides | stable | → oxide + H₂O (e.g. Cu(OH)₂ → CuO + H₂O) | → metal + O₂ + H₂O |
| Nitrates | → nitrite + O₂ | → oxide + NO₂ + O₂ | → metal + NO₂ + O₂ |
10. Corrosion
- Corrosion: slow eating away of a metal surface by air, moisture or chemicals.
- Rusting = corrosion of iron: 4Fe + 3O₂ + 2xH₂O → 2Fe₂O₃·xH₂O (brown, flaky → keeps exposing fresh iron). Needs both air (O₂) and water.
- Other corrosion: Pb → basic lead carbonate (white); Cu → green basic copper carbonate; Ag → black Ag₂S (tarnish).
- Faster when: salt/electrolyte present (sea air), pollutants (CO₂, NO₂), reactive metal, impurities.
- Prevention: (i) Barrier — oiling, painting, electroplating; (ii) Galvanisation — coating iron with zinc; (iii) Sacrificial / cathodic protection — attach a more reactive metal (Zn, Mg) that corrodes instead (used for pipelines, ships).
- Advantage: Al and Zn form a sticky, impervious oxide layer that protects the metal beneath.
11. Occurrence & Ores
- Mineral: any natural compound of a metal. Ore: a mineral from which the metal is extracted profitably.
- Gangue: earthy impurities (sand, silica). Flux: added to remove gangue → flux + gangue → slag (fusible). Smelting: reduction of roasted oxide using a flux.
| Metal | Main ore(s) |
|---|---|
| Na | Rock salt NaCl |
| Ca | Limestone CaCO₃ |
| Al | Bauxite Al₂O₃·2H₂O, Cryolite Na₃AlF₆ |
| Zn | Zinc blende ZnS, Calamine ZnCO₃ |
| Fe | Haematite Fe₂O₃ |
| Pb | Galena PbS |
| Cu | Copper pyrites CuFeS₂ |
| Ag | Argentite Ag₂S |
12. Steps of Extraction (Metallurgy)
Ore → Crushing/grinding → Concentration → Roasting/Calcination → Reduction → Refining → Pure metal- Concentration (dressing): gravity separation, froth flotation (sulphide ores), magnetic separation (e.g. iron ores), chemical/leaching.
- Roasting: heat ore strongly in air (sulphide → oxide, e.g. 2ZnS + 3O₂ → 2ZnO + 2SO₂).
- Calcination: heat in limited/no air (carbonate/hydrated → oxide, e.g. ZnCO₃ → ZnO + CO₂).
- Reduction: oxide → metal (carbon reduction or electrolytic reduction for reactive metals).
13. Extraction of Aluminium (from Bauxite)
(a) Purification — Baeyer's process: bauxite + hot NaOH → soluble sodium aluminate (Al₂O₃ + 2NaOH → 2NaAlO₂ + H₂O); insoluble Fe₂O₃/SiO₂ filtered off. Seeding/dilution precipitates Al(OH)₃, which on heating gives pure alumina (Al₂O₃). (b) Electrolytic reduction (Hall–Héroult):- Electrolyte: molten Al₂O₃ dissolved in molten cryolite (Na₃AlF₆) + fluorspar (CaF₂) — these lower the melting point (~2050 °C → ~950 °C) and increase conductivity.
- Cathode: carbon (graphite) lining → Al³⁺ + 3e⁻ → Al (molten Al collects at the bottom).
- Anode: carbon blocks → 2O²⁻ → O₂ + 4e⁻; the O₂ burns the carbon anode to CO₂, so anodes are replaced periodically.
14. Common Alloys
| Alloy | Composition | Uses |
|---|---|---|
| Steel | Fe + C (0.1–1.5%) | construction, tools |
| Stainless steel | Fe + Cr + Ni | cutlery, utensils |
| Duralumin | Al + Cu + Mg + Mn | aircraft (light & strong) |
| Brass | Cu + Zn | utensils, fittings |
| Bronze | Cu + Sn | statues, coins, medals |
| Solder | Pb + Sn | joining/soldering wires |
| Fuse metal | Pb + Sn + Bi | safety fuses (low M.P) |
Quick recall: Activity series order; metals above Al → electrolysis, below Al → C/CO/H₂. Rusting needs air + water. Aluminium: bauxite → Baeyer's → electrolysis in cryolite (cathode Al, anode O₂). Roasting = in air (sulphides); calcination = without air (carbonates).