Physical Analysis

SaltColour of solidColour of Aqueous salt solution
Salts containing Na+\text{Na}^+, K+\text{K}^+, Ca2+\text{Ca}^{2+}, Mg2+\text{Mg}^{2+}, Al3+\text{Al}^{3+}, Zn2+\text{Zn}^{2+}, NH4+\text{NH}_4^+WhiteColourless
CuSO4\text{CuSO}_4, Cu(NO3)2\text{Cu(NO}_3)_2Blue (Hydrated salts)Blue
CuCl2\text{CuCl}_2GreenBlue
CuCO3\text{CuCO}_3Greeninsoluble
FeSO4\text{FeSO}_4, Fe(NO3)2\text{Fe(NO}_3)_2, FeCl2\text{FeCl}_2GreenGreen
FeCl3\text{FeCl}_3BrownYellow
PbO\text{PbO}Yellow when hot and red when coldinsoluble
CuO\text{CuO}Blackinsoluble
ZnO\text{ZnO}Yellow when hot and white when coldinsoluble
PbCl2\text{PbCl}_2WhiteInsoluble in cold water, but soluble in hot water to give a colourless solution
PbI2\text{PbI}_2YellowInsoluble in cold water but soluble in hot water to give a colourless solution

Chemical Analysis

Cations

Sodium Hydroxide

IonsObservations<
Add \ceNaOH(aq)\ce{NaOH(aq)} dropwiseAdd \ceNaOH(aq)\ce{NaOH(aq)} until in excess
\ceCa2+\ce{Ca^2+}A white precipitate of \ceCa(OH)2(s)\ce{Ca(OH)2(s)} was formed.

\ceCa2+(aq)+2OH−(aq)−>Ca(OH)2(s)\ce{Ca^2+(aq) + 2OH^-(aq) -> Ca(OH)2(s)}
White precipitate was insoluble in excess \ceNaOH(aq)\ce{NaOH(aq)}
\ceZn2+\ce{Zn^2+}A white precipitate of \ceZn(OH)2(s)\ce{Zn(OH)2(s)} was formed.

\ceZn2+(aq)+2OH−(aq)−>Zn(OH)2(s)\ce{Zn^2+(aq) + 2OH^-(aq) -> Zn(OH)2(s)}
White precipitate was soluble in excess \ceNaOH(aq)\ce{NaOH(aq)} to give a colourless solution (zincate ions).

\ceZn(OH)2(s)+2OH−(aq)−>Zn(OH)42−(aq)\ce{Zn(OH)2(s) + 2OH^-(aq) -> Zn(OH)4^2-(aq)}
\ceAl3+\ce{Al^3+}A white precipitate of \ceAl(OH)3(s)\ce{Al(OH)3(s)} was formed.

\ceAl3+(aq)+3OH−(aq)−>Al(OH)3(s)\ce{Al^3+(aq) + 3OH^-(aq) -> Al(OH)3(s)}
White precipitate was soluble in excess \ceNaOH(aq)\ce{NaOH(aq)} to give a colourless solution (aluminate ions).

\ceAl(OH)3(s)+OH−(aq)−>Al(OH)4−(aq)\ce{Al(OH)3(s) + OH^-(aq) -> Al(OH)4^-(aq)}
\cePb2+\ce{Pb^2+}A white precipitate of \cePb(OH)2(s)\ce{Pb(OH)2(s)} was formed.

\cePb2+(aq)+2OH−(aq)−>Pb(OH)2(s)\ce{Pb^2+(aq) + 2OH^-(aq) -> Pb(OH)2(s)}
White precipitate was soluble in excess \ceNaOH(aq)\ce{NaOH(aq)} to give a colourless solution (plumbate ions).

\cePb(OH)2(s)+2OH−(aq)−>Pb(OH)42−(aq)\ce{Pb(OH)2(s) + 2OH^-(aq) -> Pb(OH)4^2-(aq)}
\ceFe2+\ce{Fe^2+}A green precipitate of \ceFe(OH)2(s)\ce{Fe(OH)2(s)} was formed.

\ceFe2+(aq)+2OH−(aq)−>Fe(OH)2(s)\ce{Fe^2+(aq) + 2OH^-(aq) -> Fe(OH)2(s)}
Green precipitate was insoluble in excess \ceNaOH(aq)\ce{NaOH(aq)}
\ceFe3+\ce{Fe^3+}A red-brown precipitate of \ceFe(OH)3(s)\ce{Fe(OH)3(s)} was formed.

\ceFe3+(aq)+3OH−(aq)−>Fe(OH)3(s)\ce{Fe^3+(aq) + 3OH^-(aq) -> Fe(OH)3(s)}
Red-brown precipitate was insoluble in excess \ceNaOH(aq)\ce{NaOH(aq)}
\ceCu2+\ce{Cu^2+}A blue precipitate of \ceCu(OH)2(s)\ce{Cu(OH)2(s)} was formed.

\ceCu2+(aq)+2OH−(aq)−>Cu(OH)2(s)\ce{Cu^2+(aq) + 2OH^-(aq) -> Cu(OH)2(s)}
Blue precipitate was insoluble in excess \ceNaOH(aq)\ce{NaOH(aq)}
\ceNH4+\ce{NH4^+}No precipitate formed.

\ceNH4+(aq)+OH−(aq)−>NH3(g)+H2O(l)\ce{NH4^+(aq) + OH^-(aq) -> NH3(g) + H2O(l)}

Note: Colourless and pungent gas which turns damp red litmus paper blue is formed upon heating. Ammonia gas (\ceNH3\ce{NH3}) evolved.
Not Applicable.

Aqueous ammonia

IonsObservations
Add \ceNH3(aq)\ce{NH3(aq)} dropwiseAdd \ceNH3(aq)\ce{NH3(aq)} until in excess
\ceCa2+\ce{Ca^2+}No precipitate formed.Not Applicable.
\ceZn2+\ce{Zn^2+}A white precipitate of \ceZn(OH)2(s)\ce{Zn(OH)2(s)} was formed.

\ceZn2+(aq)+2OH−(aq)−>Zn(OH)2(s)\ce{Zn^2+(aq) + 2OH^-(aq) -> Zn(OH)2(s)}
White precipitate was soluble in excess \ceNH3(aq)\ce{NH3(aq)} to give a colourless solution.

\ceZn(OH)2(s)+4NH3(aq)−>Zn(NH3)42+(aq)+2OH−(aq)\ce{Zn(OH)2(s) + 4NH3(aq) -> Zn(NH3)4^2+(aq) + 2OH^-(aq)}
\ceAl3+\ce{Al^3+}A white precipitate of \ceAl(OH)3(s)\ce{Al(OH)3(s)} was formed.

\ceAl3+(aq)+3OH−(aq)−>Al(OH)3(s)\ce{Al^3+(aq) + 3OH^-(aq) -> Al(OH)3(s)}
White precipitate was insoluble in excess \ceNH3(aq)\ce{NH3(aq)}.
\cePb2+\ce{Pb^2+}A white precipitate of \cePb(OH)2(s)\ce{Pb(OH)2(s)} was formed.

\cePb2+(aq)+2OH−(aq)−>Pb(OH)2(s)\ce{Pb^2+(aq) + 2OH^-(aq) -> Pb(OH)2(s)}
White precipitate was insoluble in excess \ceNH3(aq)\ce{NH3(aq)}.
\ceFe2+\ce{Fe^2+}A green precipitate of \ceFe(OH)2(s)\ce{Fe(OH)2(s)} was formed.

\ceFe2+(aq)+2OH−(aq)−>Fe(OH)2(s)\ce{Fe^2+(aq) + 2OH^-(aq) -> Fe(OH)2(s)}
Green precipitate was insoluble in excess \ceNH3(aq)\ce{NH3(aq)}.
\ceFe3+\ce{Fe^3+}A red-brown precipitate of \ceFe(OH)3(s)\ce{Fe(OH)3(s)} was formed.

\ceFe3+(aq)+3OH−(aq)−>Fe(OH)3(s)\ce{Fe^3+(aq) + 3OH^-(aq) -> Fe(OH)3(s)}
Red-brown precipitate was insoluble in excess \ceNH3(aq)\ce{NH3(aq)}.
\ceCu2+\ce{Cu^2+}A blue precipitate of \ceCu(OH)2(s)\ce{Cu(OH)2(s)} was formed.

\ceCu2+(aq)+2OH−(aq)−>Cu(OH)2(s)\ce{Cu^2+(aq) + 2OH^-(aq) -> Cu(OH)2(s)}
Blue precipitate was soluble in excess \ceNH3(aq)\ce{NH3(aq)} to give a dark blue solution.

\ceCu(OH)2(s)+4NH3(aq)−>Cu(NH3)42+(aq)+2OH−(aq)\ce{Cu(OH)2(s) + 4NH3(aq) -> Cu(NH3)4^2+(aq) + 2OH^-(aq)}
\ceNH4+\ce{NH4^+}No precipitate formed.Not Applicable.

Other tests

Further Tests for Cations

  • Dilute \ceH2SO4\ce{H2SO4} Test
    • White precipitate indicates \ceBa2+\ce{Ba^2+} or \cePb2+\ce{Pb^2+} due to formation of insoluble \ceBaSO4\ce{BaSO4} or \cePbSO4\ce{PbSO4}
  • Dilute \ceHCl\ce{HCl} Test
    • White precipitate indicates \cePb2+\ce{Pb^2+} due to insoluble \cePbCl2\ce{PbCl2} formation
      • Precipitate will be soluble upon heating as increase in temperature enhances solubility
      • Heating causes solution to become saturated, and upon heating, white crystals will appear
  • Aqueous \ceKI\ce{KI} Test
    • Yellow precipitate indicates \cePb2+\ce{Pb^2+} due to formation of insoluble \cePbI2\ce{PbI2}, which dissolves on heating and forms yellow crystals upon cooling
    • White precipitate in a brown solution indicates \ceCu2+\ce{Cu^2+} where \ceCu2+\ce{Cu^2+} is reduced to \ceCu+\ce{Cu^+} and \ceI−\ce{I^-} is oxidised to \ceI2\ce{I2}
      • \ce2Cu2+(aq)+4I−(aq)−>Cu2I2(s)+I2(aq)\ce{2Cu^2+(aq) + 4I^-(aq) -> Cu2I2(s) + I2(aq)}
    • Brown solution alone indicates an oxidising agent like \ceFe3+\ce{Fe^3+} where \ceFe3+\ce{Fe^3+} is reduced to \ceFe2+\ce{Fe^2+} and \ceI−\ce{I^-} is oxidised to \ceI2\ce{I2}
      • \ce2Fe3+(aq)+2I−(aq)−>2Fe2+(aq)+I2(aq)\ce{2Fe^3+(aq) + 2I^-(aq) -> 2Fe^2+(aq) + I2(aq)}
  • Acidified aqueous \ceKMnO4\ce{KMnO4} / \ceK2Cr2O7\ce{K2Cr2O7} Test
    • Tests for reducing agents like \ceFe2+\ce{Fe^2+}, which are oxidised to \ceFe3+\ce{Fe^3+}
      • Purple \ceKMnO4\ce{KMnO4} solution is decolourised
      • orange \ceK2Cr2O7\ce{K2Cr2O7} solution turns green

Anions

IonsReagent usedObservations
\ceCO32−\ce{CO3^{2-}}Add dilute \ceHNO3(aq)\ce{HNO3(aq)} or any other mineral acid to 1 cm31\text{ cm}^3 of the unknown. Test the gas evolved using limewater.Effervescence of a colourless and odourless gas, which gave a white precipitate with limewater. The gas is \ceCO2\ce{CO2}.

\ce2H+(aq)+CO32−(aq)−>CO2(g)+H2O(l)\ce{2H+(aq) + CO3^{2-}(aq) -> CO2(g) + H2O(l)}
\ceCl−\ce{Cl^-}Add dilute \ceHNO3(aq)\ce{HNO3(aq)}, followed by aqueous silver nitrate solution.White precipitate of \ceAgCl(s)\ce{AgCl(s)} was formed.

\ceAg+(aq)+Cl−(aq)−>AgCl(s)\ce{Ag+(aq) + Cl^-(aq) -> AgCl(s)}
\ceI−\ce{I^-}Add dilute \ceHNO3(aq)\ce{HNO3(aq)}, followed by aqueous silver nitrate solution.

Confirmation Test: Add dilute \ceHNO3(aq)\ce{HNO3(aq)}, followed by aqueous lead (II) nitrate solution (not used in the lab).
Yellow precipitate of \ceAgI(s)\ce{AgI(s)} was formed.

\ceAg+(aq)+I−(aq)−>AgI(s)\ce{Ag+(aq) + I^-(aq) -> AgI(s)}

Yellow precipitate of \cePbI2(s)\ce{PbI2(s)} was formed.

\cePb2+(aq)+2I−(aq)−>PbI2(s)\ce{Pb^{2+}(aq) + 2I^-(aq) -> PbI2(s)}
\ceSO42−\ce{SO4^{2-}}Add dilute \ceHNO3(aq)\ce{HNO3(aq)} followed by aqueous barium nitrate or aqueous barium chloride solution.White precipitate of \ceBaSO4(s)\ce{BaSO4(s)} was formed.

\ceBa2+(aq)+SO42−(aq)−>BaSO4(s)\ce{Ba^{2+}(aq) + SO4^{2-}(aq) -> BaSO4(s)}
\ceNO3−\ce{NO3^-}Add \ceNaOH(aq)\ce{NaOH(aq)} followed by aluminium powder/foil. Warm carefully. Test the gas evolved using a damp red litmus paper.Colourless and pungent gas was evolved which turned the damp red litmus paper blue. Gas evolved is \ceNH3(g)\ce{NH3(g)}.

\ce8Al(s)+3NO3−(aq)+5OH−(aq)+18H2O(l)−>3NH3(g)+8[Al(OH)4]−(aq)\ce{8Al(s) + 3NO3^-(aq) + 5OH^-(aq) + 18H2O(l) -> 3NH3(g) + 8[Al(OH)4]^-(aq)}

Gases

IonsReagent usedObservations
\ceCO2\ce{CO2}Test the gas evolved using limewater (\ceCa(OH)2(aq)\ce{Ca(OH)2(aq)}).Colourless, odourless gas evolved that gave a white precipitate with limewater.

\ceCO2(g)+Ca(OH)2(aq)−>CaCO3(s)+H2O(l)\ce{CO2(g) + Ca(OH)2(aq) -> CaCO3(s) + H2O(l)}
\ceNH3\ce{NH3}Test the gas evolved with damp red litmus paper.Colourless, pungent gas evolved that turned damp red litmus paper blue.
\ceCl2\ce{Cl2}Test the gas evolved with damp litmus paper.Greenish yellow, pungent gas evolved that turned damp blue litmus paper red, and then bleached it.
\ceH2\ce{H2}Test with a lighted splint.Colourless, odourless gas evolved that extinguished the lighted splint with a 'pop' sound.
\ceO2\ce{O2}Test with a glowing splint.Colourless, odourless gas evolved that relights the glowing splint.
\ceSO2\ce{SO2}Test gas evolved with acidified potassium manganate(VII), \ceKMnO4\ce{KMnO4}Colourless, pungent gas evolved that turned purple \ceKMnO4\ce{KMnO4} solution colourless.
\ceNO2\ce{NO2}Pungent, brown gas
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