Grade 10 Chemistry Notes: Metals, Nonmetals, and Their Production

5.2 General Properties of Metals and Production of Some Metals

  • Students should be able to:
    • Mention general properties of metals.
    • Describe the uses of some common metals.
  • This section covers general characteristics and extraction of metals, uses of some common metals, alloys, and production of Aluminum, Copper, and Iron.

5.2.1 Properties and Extraction of Metals

  • Activity 5.1: Discuss metal properties in groups.
    • A metal which is liquid at room temperature.
    • A metal that exists in the gaseous state at room temperature.
    • A metal which is the best conductor of heat.
    • A metal which is the poorest conductor of heat.
    • A metal which can be cut with a knife.
  • About 80% of known elements are metals.
A. Some Physical Properties of Metals
  • Lustrous Appearance:
    • Metals have a shining appearance and can be polished.
    • Gold is shining yellow, copper is brown.
    • Iron, aluminum, zinc, and silver are lustrous grey or silvery.
  • Malleability:
    • Metals can be beaten into thin sheets.
    • Examples: Aluminum foils, gold and silver ornaments.
  • Ductility:
    • Metals can be drawn into wires.
    • Examples: Copper, gold, iron, and silver.
  • Hardness and Tensile Strength:
    • Metals are generally hard and have tensile strength, except lithium, potassium, sodium.
  • Density:
    • Metals generally have a high density except lithium, potassium, sodium.
  • Sonorous:
    • Metals produce a metallic sound when struck (e.g., school bell).
B. Chemical Properties of Metals
  • Positive Valency:
    • Metals possess positive valency and have a tendency to lose electrons.
    • M(g)Mn+(g)+neM(g) \rightarrow M^{n+}(g) + ne^-
  • Valence Electrons:
    • Metals have 1, 2, or 3 valence electrons.
  • Reducing Agents:
    • Metals are oxidized by losing electrons and act as reducing agents.
  • Oxides Formation:
    • They mostly form basic oxides and some amphoteric oxides.
  • Chlorides Formation:
    • They form chlorides that are true salts and electrovalent.
  • Hydrides Formation:
    • They form hydrides which are ionic, unstable, and reactive.
  • Reaction with Acids:
    • They usually replace hydrogen from dilute non-oxidizing acids like HClHCl and H<em>2SO</em>4H<em>2SO</em>4. Exceptions are copper, silver, and gold.
C. Reactivity Series of Metals
  • Activity Series:
    • Arrangement of metals in decreasing order of activity.
    • The most active metal is at the top, and the least active metal is at the bottom.
    • Hydrogen is included for comparison.
  • Reaction with Dilute Acids:
    • Metals above hydrogen (potassium, sodium, calcium, magnesium) liberate hydrogen gas when treated with dilute acids.
    • Metals below hydrogen (copper, silver, gold) do not liberate hydrogen.
  • Displacement Reactions:
    • A more reactive metal can displace a less reactive metal from its compound or salt solution.
    • Potassium can displace all metals from their salt solutions.
  • Reducing Agent Strength:
    • Metals at the top of the reactivity series are strong reducing agents.
    • Metals at the bottom are weak reducing agents.
    • Potassium is the strongest, and gold is the weakest reducing agent.
D. Natural Occurrence and Extraction of Metals
  • Uncombined State:
    • Noble metals (Ag, Au, Bi, Cu, Pd, Pt) exist in nature as uncombined or free state.
  • Combined State:
    • Active metals (alkali and alkaline earth metals) never exist in uncombined state.
    • They exist in the form of carbonates, halides, oxides, phosphates, silicates, sulphides, and sulphates.
  • Minerals:
    • Constituents of the earth’s crust containing metals or their compounds.
    • Examples: Sodium as halite (NaClNaCl), potassium as sylvite (KClKCl), magnesium as magnesite (MgCO<em>3MgCO<em>3), calcium as limestone (CaCO</em>3CaCO</em>3).
  • Ores:
    • Minerals with a high percentage of a particular metal from which the metal can be profitably extracted.
    • Ores contain impurities (sand and other undesirable materials) called gangue.
  • Metallurgy:
    • The science and technology of extracting metals from their ores and compounding alloys.
  • Principal Steps in Extraction:
    1. Preparation (concentration) of the ore (e.g., oil floatation, magnetic separation).
    2. Production of the metal (e.g., roasting, calcination).
    3. Purification of the metal (e.g., chemical reduction, electrolytic reduction).
  • Extraction by Electrolysis:
    • Most active metals (K, Na, Ca, Mg) are extracted only by electrolysis.

5.2.2 Alloys

  • Definition:
    • Mixtures of two or more metals or metals and nonmetals when molten and do not separate when solidified.
  • Formation:
    • The constituent elements are melted together and then allowed to cool to form a solid material called alloy.
  • Effect of Alloying:
    • Increases hardness and strength.
    • Modifies color and melting point.
    • Decreases electrical conductivity.
    • Increases resistance to corrosion of metals.
  • Examples of Alloys:
    • Amalgam: Alloy of mercury and another metal.
    • Gun Metal: Alloy of copper (87%), tin (10%), and zinc (3%).
    • Solder (Fuse Metal): 67% tin and 33% lead, melts at 183°C (lower than tin's melting point of 232°C). Used to join wires and electrical resistances.
  • Gold Alloys:
    • Gold is hardened by alloying it with copper and silver.
    • Gold content is expressed in carats or mass percent.
    • Carat: Mass unit of gold in 24 mass units of the alloy.
    • 24 carat: Pure gold.
    • 22 carat: 22 parts of pure gold in 24 parts of the alloy.
  • Mass Percent Calculation Examples:
    • Mass % of gold in 24 carat gold = 24×10024=100.00\frac{24 \times 100}{24} = 100.00
    • Mass % of gold in 22 carat gold = 22×10024=91.67\frac{22 \times 100}{24} = 91.67

5.2.3 Production of Aluminum, Iron, and Copper

A. Aluminum
  • Students should be able to:
    • Explain properties, occurrence, and extraction of aluminum.
    • Describe the applications of aluminum.
  • Occurrence:
    • Most abundant metal in the earth's crust (about 8%).
    • Third most abundant element after oxygen and silicon.
    • Does not occur in uncombined or free metal state.
    • Main mineral is bauxite (Al2O3
      2H_2O).
    • Other minerals: orthoclase (KAlSi<em>3O</em>8KAlSi<em>3O</em>8), cryolite (Na<em>3AlF</em>6Na<em>3AlF</em>6), corundum (Al<em>2O</em>3Al<em>2O</em>3), beryl (Be<em>3Al</em>2Si<em>6O</em>8Be<em>3Al</em>2Si<em>6O</em>8), and china clay (Al2Si2O7 2H2O).
  • Extraction (Hall–Héroult Process):
    1. Purification of Bauxite:
      • Bauxite is contaminated by silicon dioxide (SiO2SiO_2), iron oxide, and titanium (IV) oxide.
      • Powdered ore is heated with sodium hydroxide solution to convert silica to soluble silicate.
      • SiO<em>2(s)+2NaOH(aq)Na</em>2SiO<em>3(aq)+H</em>2O(l)SiO<em>2(s) + 2NaOH(aq) \rightarrow Na</em>2SiO<em>3(aq) + H</em>2O(l)
      • Aluminum oxide is converted to soluble sodium aluminate.
      • Al<em>2O</em>3(s)+2NaOH(aq)2NaAlO<em>2(aq)+H</em>2O(l)Al<em>2O</em>3(s) + 2NaOH(aq) \rightarrow 2NaAlO<em>2(aq) + H</em>2O(l)
      • Impurities like iron oxides and titanium (IV) oxide remain unaffected and are filtered off.
      • The solution is treated with acid to precipitate aluminum hydroxide.
      • AlO<em>2(aq)+H</em>3O+(aq)Al(OH)3(s)AlO<em>2^-(aq) + H</em>3O^+(aq) \rightarrow Al(OH)_3(s)
      • Aluminum hydroxide is collected, washed, dried, and heated to get Al<em>2O</em>3Al<em>2O</em>3.
      • 2Al(OH)<em>3(s)HeatAl</em>2O<em>3(s)+3H</em>2O(g)2Al(OH)<em>3(s) \xrightarrow{Heat} Al</em>2O<em>3(s) + 3H</em>2O(g)
    2. Electrolysis:
      • Pure aluminum oxide is mixed with cryolite (Na<em>3AlF</em>6Na<em>3AlF</em>6) to reduce its melting point from 2045°C to 1000°C.
      • The molten cryolite provides a good conducting medium for electrolysis.
      • Graphite electrodes are used as both anode and cathode.
      • Electrode Reactions:
        • Anode: 3C(s)+6O23CO2(g)+12e3C(s) + 6O^{2-} \rightarrow 3CO_2(g) + 12e^-
        • Cathode: 4Al3+(l)+12e4Al(l)4Al^{3+}(l) + 12e^- \rightarrow 4Al(l)
      • Overall Reaction:
        • 4Al3+(l)+6O2(l)+3C(s)4Al(l)+3CO2(g)4Al^{3+}(l) + 6O^{2-}(l) + 3C(s) \rightarrow 4Al(l) + 3CO_2(g)
        • 2Al<em>2O</em>3(l)+3C(s)4Al(l)+3CO2(g)2Al<em>2O</em>3(l) + 3C(s) \rightarrow 4Al(l) + 3CO_2(g)
      • The anode (graphite electrode) oxidizes to carbon dioxide and must be replaced regularly.
      • Molten aluminum is siphoned from the bottom of the electrolytic cell.
  • Physical Properties:
    • Soft, silvery-white, and light metal with a density of 2.7 g/cm3.
    • Melts at 660°C.
    • Can be shaped into wires, rolled, pressed, or cast into different shapes.
    • Good conductor of heat and electricity.
  • Chemical Properties:
    • Reactive metal.
    • Reaction with Oxygen:
      • Reacts with atmospheric oxygen to form a thin film of aluminum oxide on its surface (4Al(s)+3O<em>2(g)2Al</em>2O3(s)4Al(s) + 3O<em>2(g) \rightarrow 2Al</em>2O_3(s)).
      • This film inhibits further reaction with oxygen.
    • Reaction with Nitrogen:
      • Burns in nitrogen gas to form aluminum nitride (2Al(s)+N2(g)2AlN(s)2Al(s) + N_2(g) \rightarrow 2AlN(s)).
    • Reaction with Dilute Acids:
      • Reacts with dilute acids like HClHCl and H<em>2SO</em>4H<em>2SO</em>4, forming salts and liberating hydrogen gas.
      • 2Al(s)+3H<em>2SO</em>4(aq)Al<em>2(SO</em>4)<em>3(aq)+3H</em>2(g)2Al(s) + 3H<em>2SO</em>4(aq) \rightarrow Al<em>2(SO</em>4)<em>3(aq) + 3H</em>2(g)
      • 2Al(s)+6HCl(aq)2AlCl<em>3(s)+3H</em>2(g)2Al(s) + 6HCl(aq) \rightarrow 2AlCl<em>3(s) + 3H</em>2(g)
      • Does not react with dilute or concentrated HNO3HNO_3 due to the formation of a protective oxide layer.
    • Reaction with Chlorine:
      • Burns in chlorine gas to form aluminum chloride (2Al(s)+3Cl<em>2(g)2AlCl</em>3(s)2Al(s) + 3Cl<em>2(g) \rightarrow 2AlCl</em>3(s)).
    • Reaction with Sodium Hydroxide Solution:
      • 2Al(s)+2NaOH(aq)+6H<em>2O(l)2NaAl(OH)</em>4(aq)+3H2(g)2Al(s) + 2NaOH(aq) + 6H<em>2O(l) \rightarrow 2NaAl(OH)</em>4(aq) + 3H_2(g)
  • Uses of Aluminum:
    • Light alloys like duralumin (Al, Cu, Mg) are used in the transportation industry (airplanes, ships, automobiles).
    • High thermal conductivity and corrosion resistance make it suitable for household cookware.
    • Manufacture of door and window frames and building roofs.
    • Packaging material in the food industry.
    • Power transmission lines.
    • Thermite Welding:
      • Aluminum displaces iron from iron oxide. 2Al(s)+Fe<em>2O</em>3(s)2Fe(l)+Al<em>2O</em>3(s)2Al(s) + Fe<em>2O</em>3(s) \rightarrow 2Fe(l) + Al<em>2O</em>3(s)
      • Mixture of powdered aluminum and iron oxide is called thermite and produces a temperature of about 3000°C.
      • Used in welding rails, propeller shafts, and other steel parts.
B. Iron
  • Students should be able to:
    • Explain properties, occurrence, and extraction of iron.
    • Describe the applications of iron.
  • Occurrence:
    • Second most abundant metal in the earth's crust after aluminum (about 4.7% of the earth's crust).
    • Never found as a free metal in nature.
    • Exists in the form of compounds (oxides, carbonates, and sulphides).
    • Chief ores are hematite (Fe<em>2O</em>3Fe<em>2O</em>3), limonite (Fe2O3
      H2O), magnetite (Fe</em>3O<em>4Fe</em>3O<em>4), and siderite (FeCO</em>3FeCO</em>3).
    • Also found as iron pyrites (FeS2FeS_2), commonly called fool’s gold.
  • Extraction (Blast Furnace):
    • Raw materials: iron ore, coke, limestone, and hot air.
    • The furnace is charged with a mixture of iron ore, limestone, and coke at the top, and hot air is blown at the bottom.
    • Reactions in the Blast Furnace:
      1. Oxidation of coke to carbon dioxide: C(s)+O<em>2(g)CO</em>2(g)+HeatC(s) + O<em>2(g) \rightarrow CO</em>2(g) + Heat
      2. Reduction of carbon dioxide to carbon monoxide: CO2(g)+C(s)2CO(g)CO_2(g) + C(s) \rightarrow 2CO(g)
      3. Reduction of iron oxides to metallic iron by carbon monoxide:
        • 3Fe<em>2O</em>3(s)+CO(g)2Fe<em>3O</em>4(s)+CO2(g)3Fe<em>2O</em>3(s) + CO(g) \rightarrow 2Fe<em>3O</em>4(s) + CO_2(g)
        • Fe<em>3O</em>4(s)+CO(g)3FeO(s)+CO2(g)Fe<em>3O</em>4(s) + CO(g) \rightarrow 3FeO(s) + CO_2(g)
        • FeO(s)+CO(g)Fe(l)+CO2(g)FeO(s) + CO(g) \rightarrow Fe(l) + CO_2(g)
      4. Decomposition of limestone:
        • CaCO<em>3(s)CaO(s)+CO</em>2(g)CaCO<em>3(s) \rightarrow CaO(s) + CO</em>2(g)
      5. Formation of slag:
        • CaO+SiO<em>2CaSiO</em>3CaO + SiO<em>2 \rightarrow CaSiO</em>3
        • Lime + sand calcium silicate
        • (Flux) (Impurity) (Slag)
    • Slag is used for the manufacture of cement.
    • The iron obtained directly from the blast furnace is called pig iron.
    • Pig iron contains about 2% silicon, up to 1% phosphorus and manganese, and traces of sulfur.
    • Pig iron contains high carbon content, typically 3.5 - 4.5%, making it brittle.
  • Wrought Iron:
    • The purest form of commercial iron is called wrought iron, obtained by removing most impurities from pig iron.
    • Impure iron is heated with hematite and limestone in a furnace.
    • Increases the purity of the iron to 99.5%.
    • Tough, malleable, and ductile.
  • Steel Making from Pig Iron (Purification of Pig Iron):
    • Conversion of pig iron to steel is a purification process where impurities are eliminated through oxidation at high temperatures.
    • Three techniques used: Bessemer converter, Open-hearth Furnace, and Basic Oxygen Process.
      1. Bessemer Converter:
        • Molten pig iron is transferred to a cylindrical vessel with a refractory lining of MgCO<em>3MgCO<em>3 and CaCO</em>3CaCO</em>3.
        • A blast of hot air is blown through the molten metal.
        • Oxygen converts silicon, phosphorus, and sulfur to their oxides, which react with the lining to form a slag.
        • Carbon is oxidized to carbon monoxide.
      2. Open-hearth Furnace:
        • A large, shallow hearth lined with a basic oxide refractory (MgO and CaO).
        • Charged with a mixture of pig iron, Fe<em>2O</em>3Fe<em>2O</em>3, scrap iron, and limestone.
        • A blast of hot air and burning fuel is directed over the surface.
        • Impurities are oxidized by the Fe<em>2O</em>3Fe<em>2O</em>3 and air, forming carbon dioxide and sulfur dioxide.
        • C+O<em>2CO</em>2C + O<em>2 \rightarrow CO</em>2
        • S+O<em>2SO</em>2S + O<em>2 \rightarrow SO</em>2
        • 12P+10Fe<em>2O</em>33P<em>4O</em>10+20Fe12P + 10Fe<em>2O</em>3 \rightarrow 3P<em>4O</em>{10} + 20Fe
        • 3Si+2Fe<em>2O</em>33SiO2+4Fe3Si + 2Fe<em>2O</em>3 \rightarrow 3SiO_2 + 4Fe
        • Calcium oxide (from limestone) reacts with oxides of silicon and phosphorus to form slag.
        • P<em>4O</em>10+6CaO2Ca<em>3(PO</em>4)2P<em>4O</em>{10} + 6CaO \rightarrow 2Ca<em>3(PO</em>4)_2
        • SiO<em>2+CaOCaSiO</em>3SiO<em>2 + CaO \rightarrow CaSiO</em>3
        • Impurities manganese and silicon form respective oxides and removed as slag. (a)Si+O<em>2SiO</em>2(a) Si + O<em>2 \rightarrow SiO</em>2
      3. Basic Oxygen Process:
        • A mixture of powdered calcium oxide (CaO) and oxygen gas is forced directly into the surface of the molten pig iron.
        • The oxygen reacts exothermically with carbon, sulfur, silicon, phosphorus, and impurity metals.
        • Carbon and sulfur are oxidized to CO<em>2CO<em>2 and SO</em>2SO</em>2.
        • Oxides of silicon (SiO<em>2SiO<em>2), phosphorus (P</em>4O10P</em>4O_{10}), and impurity metals combine with lime (CaO), forming slag.
  • Tempering of Steel:
    • A process by which steel is conditioned to a desired hardness by heating and controlled rate of cooling.
    • Some carbon in steel is present as cementite (FeC3FeC_3).
  • Physical Properties of Iron:
    • Gray lustrous, malleable, and ductile metal.
    • Good conductor of heat and electricity.
    • High melting point (1580°C) and high density (7.87 g/cm3).
    • Ferromagnetic metal.
  • Chemical Properties of Iron:
    • Reactive metal, but less reactive than group IA and IIA metals.
    • Rusts in the presence of air and moisture to form hydrated iron (III) oxide: 4Fe(s) + 3O2(g) + Moisture \rightarrow 2Fe2O3 xH2O(s)(rust)
    • Reacts with dilute acids to form iron (II) salts and liberating hydrogen gas
      • Fe(s)+2HCl(aq)FeCl<em>2(aq)+H</em>2(g)Fe (s) + 2HCl (aq) \rightarrow FeCl<em>2 (aq) + H</em>2 (g)
      • Fe(s)+H<em>2SO</em>4(aq)FeSO<em>4(aq)+H</em>2(g)Fe (s) + H<em>2SO</em>4 (aq) \rightarrow FeSO<em>4 (aq) + H</em>2 (g)
    • Exhibits different oxidation states (Fe2+ and Fe+3).
    • Solutions of iron (II) compounds are pale-green and solutions of iron (III) compounds are yellowish brown.
    • Heated iron reacts with hydrogen chloride gas to form iron (II) chloride and hydrogen gas.
    • Fe(s)+2HCl(g)FeCl<em>2(g)+H</em>2(g)Fe (s) + 2HCl (g) \rightarrow FeCl<em>2 (g) + H</em>2 (g)
    • Heated iron reacts with chlorine and sulfur.
      • 2Fe(s)+3Cl<em>2(g)2FeCl</em>3(s)2Fe (s) + 3Cl<em>2 (g) \rightarrow 2FeCl</em>3 (s)
      • Fe(s)+S(s)FeS(s)Fe (s) + S (s) \rightarrow FeS (s)
    • Displaces less active metals from solutions of their salts.
      • Fe(s)+Cu2+(aq)Fe2+(aq)+Cu(s)Fe (s) + Cu^{2+} (aq) \rightarrow Fe^{2+} (aq) + Cu (s)
  • Uses of Iron:
    • Widely used metal in construction of buildings and bridges
    • Pig iron is used to make domestic boilers, hot-water radiators, railings, water pipes, castings, and moldings.
    • Wrought iron is used in making nails, sheets, horseshoes, ornamental gates, door knockers, farm machinery etc.
    • Manufacture of alloys such as carbon steels and alloy steels.
C. Copper
  • Students should be able to:
    • Explain properties, occurrence and extraction of Copper.
    • Describe the the applications of Copper.
  • Occurrence:
    • Occasionally found as native copper, but mainly in compounds (sulphides, oxides and carbonates).
    • Most important sulphide ores are chalcopyrite (CuFeS<em>2CuFeS<em>2), chalcocite (Cu</em>2SCu</em>2S), covellite (CuSCuS) and bornite (Cu<em>5FeS</em>4Cu<em>5FeS</em>4).
    • Principal oxide ores are cuprite (Cu2OCu_2O) and tenorite (CuOCuO).
    • Carbonate form:
      • malachite (CuCO3 Cu(OH)2).
  • Extraction from Chalcopyrite:
    1. Concentration by Froth Flotation:
      • Crushed and ground sulphide ore is concentrated, changing the concentration from 2 % copper to as high as 30% copper.
    2. Roasting:
      • Concentrated ore is roasted with a limited supply of air (oxygen).
      • 2CuFeS<em>2(s)+4O</em>2(g)Cu<em>2S(s)+2FeO(s)+3SO</em>2(g)2CuFeS<em>2 (s) + 4O</em>2 (g) \rightarrow Cu<em>2S (s) + 2FeO(s) + 3SO</em>2 (g)
    3. Smelting:
      • Roasted mixture is smelted by adding limestone and sand to form a molten slag that removes impurities.
      • CaCO<em>3(s)+SiO</em>2(s)CaSiO<em>3(l)+CO</em>2(g)CaCO<em>3 (s) + SiO</em>2 (s) \rightarrow CaSiO<em>3 (l) + CO</em>2 (g)
      • FeO(s)+SiO<em>2(s)FeSiO</em>3(l)FeO (s) + SiO<em>2 (s) \rightarrow FeSiO</em>3 (l)
    4. Reduction:
      • The Cu2SCu_2S obtained by roasting chalcopyrite is then reduced by heating it in a limited supply of oxygen.
      • Cu<em>2S(s)+O</em>2(g)2Cu(l)+SO2(g)Cu<em>2S (s) + O</em>2 (g) \rightarrow 2Cu (l) + SO_2 (g)
      • The copper produced is called blister copper and it has 98.5 – 99.5 % purity.
    5. Electrolytic Refining:
      • Blister copper contains iron, silver, gold and sometimes zinc as impurities.
        • Anode: A thick block of impure copper.
        • Cathode: A thin strip of pure copper.
        • Electrolyte: An aqueous solution of copper sulphate, Small quantity of dilute sulphuric acid is also added to the salt solution to prevent hydrolysis.
          • Oxidation at anode:
            • Cu(impuremetal)Cu2+(aq)+2eCu (impure metal) \rightarrow Cu^{2+}(aq) + 2e^−
          • Reduction at cathode:
            • Cu2+(aq)+2eCu(metal)Cu^{2+}(aq) + 2e \rightarrow Cu ( metal)
  • Physical Properties of Copper:
    • Soft, ductile, malleable, reddish-brown metal with a density of 8.96 g/ cm3.
    • Second to silver in electrical conductivity.
    • Melts at 1086°C and boils at 2310°C.
  • Chemical Properties of Copper:
    • Less reactive metal that is why it is found in the native state.
      • Powdered copper, when heated in air forms a black powder of copper (II) oxide, CuOCuO.
      • 2Cu(s)+O2(g)2CuO(s)2Cu (s) + O_2 (g) \rightarrow 2CuO (s)
    • Does not react with dilute acids like HClHCl and H<em>2SO</em>4H<em>2SO</em>4.
    • Oxidized by oxidizing acids such as dilute and concentrated nitric acid and hot concentrated sulphuric acid, H<em>2SO</em>4H<em>2SO</em>4.
      • dilute3Cu(s)+8HNO<em>3(aq)3Cu(NO)</em>3)<em>2(aq)+2NO(g)+4H</em>2O(l)dilute 3Cu(s) + 8HNO<em>3 (aq) 3Cu(NO)</em>3)<em>2 (aq) + 2NO (g) + 4H</em>2O (l)
      • concentratedCu(s)+8HNO<em>3(aq)Cu(NO)</em>3)<em>2(aq)+2NO</em>2(g)+2H2O(l)concentrated Cu(s) + 8HNO<em>3 (aq) Cu(NO)</em>3)<em>2 (aq) + 2NO</em>2 (g) + 2H_2O (l)
      • HotandconcentratedCu(s)+2H<em>2SO</em>4(aq)CuSO<em>4(aq)+SO</em>2(g)+2H2O(l)Hot and concentrated Cu(s) + 2H<em>2SO</em>4 (aq) CuSO<em>4(aq) + SO</em>2 (g) + 2H_2O (l)
    • Corrodes in moist air over a long period of time as a result of oxidation caused by a mixture of water, oxygen and carbon dioxide. It turns green, due to the formation of verdigris: a basic copper carbonate (CuCO3 Cu(OH)2) or Cu<em>2(OH)</em>2CO3Cu<em>2(OH)</em>2CO_3.
      • 2Cu (s) + H2O (l) + O2 (g) + CO2 (g) \rightarrow CuCO3
        Cu(OH)_2
    • Exhibits different oxidation states. It exists as cuprous (Cu+Cu^+) and cupric (Cu2+Cu^{2+}) ions.
      • 2Cu+(aq)Cu2+(aq)+Cu(s)2Cu^+ (aq) \rightarrow Cu^{2+} (aq) + Cu (s)
  • Uses of Copper:
    • Alloys:
      • bronze (copper and tin).
      • brass (copper and zinc).
    • Electrical industry: electric wires, cables.
    • Copper compounds as pesticides.

5.3 Production of Some Important Nonmetals

5.3.1 General Properties of Nonmetals and Common Uses of Some Nonmetallic Compounds

  • Students should be able to:
    • Mention the general properties of non-metals and their uses.
    • Describe some common uses of compounds of nonmetals such as CO<em>2CO<em>2, Na</em>2CO<em>3Na</em>2CO<em>3, NH</em>3NH</em>3, HNO<em>3HNO<em>3, H</em>3PO<em>4H</em>3PO<em>4, Ca</em>3(PO<em>4)</em>2Ca</em>3(PO<em>4)</em>2, SO<em>2SO<em>2 & H</em>2SO4H</em>2SO_4
    • Describe the occurrence, extraction and uses of nitrogen, phosphorous, oxygen, sulphur and chlorine.
  • Nonmetals have opposite characteristics to that of metals.
A. Physical Properties
  • State:
    • Solids, liquids, gases.
  • Luster:
    • Non-lustrous.
  • Malleability and Ductility:
    • Nonmalleable and non-ductile.
  • Hardness and Density:
    • Varying hardness and have low density.
  • Melting and Boiling Points:
    • Low melting and boiling points.
  • Sonorousity:
    • Non-sonorous.
  • Conductivity:
    • Poor conductors of heat and electricity.
B. Chemical Properties of Non-Metals
  • Reaction with Oxygen:
    • Nonmetals react with oxygen on heating or burning to form their oxides.
  • Reaction with Acids:
    • Do not displace hydrogen on reaction with dilute acids.
  • Oxide Nature:
    • React with oxygen to form acidic or neutral oxides.
  • Hydride Formation:
    • Combine with hydrogen to form stable hydrides.
  • Reaction with Water:
    • Do not react with water.
  • Electronegativity:
    • Electronegative i.e for negative ions by gaining electrons.
  • Oxidizing Agents:
    • Oxidizing agents.

5.3.2 Production of Nitrogen, Phosphorous, Oxygen, Sulphur and Chlorine

A. Nitrogen
  • Students should be able to:
    • Explain properties, Occurrence and extraction of Nitrogen.
    • Describe the the applications of Nitrogen.
  • Occurrence and Production:
    • Occurs in nature in the elemental form as a diatomic molecule, N2N_2, in atmospheric air (about 80% by volume).
    • In the form of compounds, it exists as sodium nitrate (Chile salt peter, NaNO<em>3NaNO<em>3) and potassium nitrate (KNO</em>3KNO</em>3) also called saltpetre.
    • Also found in DNA molecules and proteins of all living things.
    • Industrial Production:
      • Impurities (dust, other particles, CO2CO_2, water vapor) are removed from air.
      • Air is compressed under high pressure and low temperature.
      • Fractional distillation of liquid air separates nitrogen.
      • Argon distills off the mixture at –186°C, leaving behind a blue liquid of oxygen that boils at –183°C.
    • Laboratory Preparation:
      • Warming an aqueous solution containing ammonium chloride and sodium nitrite.
      • NH<em>4Cl(aq)+NaNO</em>2(aq)NaCl(aq)+N<em>2(g)+2H</em>2O(l)NH<em>4Cl(aq) + NaNO</em>2(aq) \rightarrow NaCl(aq) + N<em>2(g) + 2H</em>2O(l)
  • Physical Properties of Nitrogen:
    • Colorless, odorless, and tasteless gas.
    • Inert under ordinary conditions due to the strength of the triple bond.
  • Chemical Properties of Nitrogen:
    • Reacts with metals of group IA and IIA as well as oxygen at higher temperatures.
    • Reaction with Reactive Metals:
      • Lithium: 6Li(s)+N<em>2(g)2Li</em>3N(s)6Li (s) + N<em>2 (g) \rightarrow 2Li</em>3N (s)
      • Calcium: 3Ca(s)+N<em>2(g)Ca</em>3N2(s)3Ca (s) + N<em>2 (g) \rightarrow Ca</em>3N_2 (s)
      • Magnesium: 3Mg(s)+N<em>2(g)Mg</em>3N2(s)3Mg (s) + N<em>2 (g) \rightarrow Mg</em>3N_2 (s)
    • Reaction with Oxygen:
      • N<em>2(g)+O</em>2(g)2NO(g)N<em>2 (g) + O</em>2 (g) \rightarrow 2NO (g)
      • N<em>2(g)+2O</em>2(g)2NO2(g)N<em>2 (g) + 2O</em>2 (g) \rightarrow 2NO_2 (g)
      • Nitric oxide (NO) forms nitrogen dioxide (NO<em>2NO<em>2), a reddish brown gas and dimerizes at low temperatures to give a colorless gas of dinitrogen tetraoxide, N</em>2O4N</em>2O_4.
      • 2NO<em>2(g)N</em>2O4(g)2NO<em>2 (g) \rightarrow N</em>2O_4 (g)
    • Forms oxides, like dinitrogen monoxide, N<em>2ON<em>2O, dinitrogen trioxide (N</em>2O<em>3N</em>2O<em>3) and dinitrogen pentoxide (N</em>2O5N</em>2O_5).
    • Haber Process:
      • Reacts directly with hydrogen in the Haber process to form ammonia.
      • N<em>2(g)+3H</em>2(g)2NH3(g) Fe/200300atm,400600CN<em>2(g) + 3H</em>2(g) \rightleftharpoons 2NH_3(g) \text{ } Fe/200 - 300atm, 400-600^\circ C
  • Uses of Nitrogen:
    • Used in food packaging to prevent oxidation.
    • To create an inert atmosphere in the production of semiconductors.
    • Liquid nitrogen is used as a refrigerant to preserve bulls’ semen and blood.
    • Major use is in the production of ammonia.
B. Phosphorus
  • Students should be able to:
    • Explain properties ,Occurrence and extraction of Phosphorous.
    • Describe the the applications of Phosphorous.
  • Occurrence and Extraction:
    • A relatively abundant element, ranking 12th in the earth’s crust.
    • Exists naturally only in the combined state, such as in rock phosphate, Ca<em>3(PO</em>4)<em>2Ca<em>3(PO</em>4)<em>2, fluoroapatite, Ca</em>10(PO<em>4)</em>6F<em>2Ca</em>{10}(PO<em>4)</em>6F<em>2 or 3Ca3(PO4)2
      CaF_2.
    • Allotropic forms: white phosphorus and red phosphorus.
  • Physical Properties of Phosphorus:
    • White Phosphorus:
      • Very poisonous, white waxy-looking substance that melts at 44.1°C and boils at 287°C.
      • Density is 1.8 g/cm3.
      • Consists of individual tetra- atomic (P4P_4) molecules and is an unstable form of phosphorus
    • Red Phosphorus:
      • Denser (2.16 g/cm3) and is much less reactive than white phosphorus at normal temperatures.
      • Consists of P4P_4 molecules linked together to form a polymer
  • Industrial Manufacture of White Phosphorus:
    • Heating a mixture of crushed rock phosphate, Ca<em>3(PO</em>4)2Ca<em>3(PO</em>4)_2, silica, SiO2, and coke in an electric furnace.
    • 2Ca<em>3(PO</em>4)<em>2(s)+6SiO</em>2(s)+10C(s)6CaSiO<em>3(l)+P</em>4(g)+10CO(g)2Ca<em>3(PO</em>4)<em>2 (s) + 6SiO</em>2 (s) + 10C (s) \rightarrow 6CaSiO<em>3(l) + P</em>4(g) + 10CO (g)
    • The vaporized phosphorus ($$