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PRELIMINARY OBSERVATIONS:
1 Noted the colour of the salt Colourless May not be Cu2+, Ni2+etc
3 Solubility
A little of the substance is made into a b) Brick red flame May be Ca2+
paste with conc.HCl [in a china dish]
and shown to the non-luminous part of c) Crimson red flame May be Sr2+
the flame using a glass rod
CH3COO- + H+ → CH3COOH
3 A little of the substance is treated with Colourless pungent Presence of chloride (Cl-)
conc. H2SO4 smelling gas forming
thick white fumes with a Cl- + H+ → HCl
glass rod dipped in
NH4OH NH3+HCl → NH4Cl
4 A little of the substance is warmed with Reddish brown vapours Presence of nitrate (NO3-)
conc. H2SO4 and then add Cu turnings (solution turns blue)
4H+ + 2 NO3- +Cu → 2NO2 +
Cu2+ +2H2O
6 An aqueous solution of the substance is White ppt insoluble in Presence of sulphate (SO42-)
treated with dil.HCl and excess of BaCl2 excess of dil.HCl
SO42- + Ba2+ → BaSO4
solution
2 Chloride: An aqueous solution of the White curdy ppt soluble in Chloride (Cl-) is confirmed
substance is treated with dil. HNO3 and excess of NH4OH
AgNO3 solution Ag+ + Cl- → AgCl
2 Lead (Pb2+):
Dissolve the white ppt (obtained in group I analysis) in boiling water and divide into two parts
a) To the first part, add KI Yellow ppt soluble in hot Pb2+ is confirmed
water and re-crystallises
as golden sprangles on Pb2++2I- → PbI2
cooling
5 Ca2+/Ba2+and Sr2+:
Dissolve the white ppt of group V in minimum amount of dil. acetic acid, boil to expel CO2 and
divide into 3 parts
a) Ba2+: To the first part add K2CrO4 Yellow ppt Ba2+ confirmed
solution Ba2++CrO42- → BaCrO4
b) Sr2+: To the second part add Scanty white ppt (appears Sr2+ confirmed
ammonium sulphate solution slowly in cold but readily
on boiling) Sr2++SO42- → SrSO4
c) Ca2+: To the third part add ammonium White ppt Ca2+ confirmed
oxalate solution
Ca2++C2O42- → CaC2O4