salt analysis questions
salt analysis questions
49. Why is the hot reaction mixture in case of conc. H2SO4 test not thrown into the sink?
Ans. In order to avoid spurting, due to which H2SO4 may fly and spoil clothes and may result into
serious injuries.
50. What is Tollen’s reagent?
Ans. Ammonical AgNO3 solution is called Tollen’s reagent.
51. Why does a dark brown ring form at the junction of two layers in ring test for nitrates?
Ans. H2SO4 being heavier forms the lower layer and reacts only with a small amount of nitrate and
FeSO4 at its surface, therefore, a brown ring appears at the junction of the two layers.
52. What is the formula of sodium nitroprusside?
Ans. Na2[Fe(CN)5 NO].
53. What is chromyl chloride test?
Ans. Heat a small amount of the mixture with conc. H2SO4 and solid K2Cr2O7 in a dry test tube.
Deep brownish red vapours of chromyl chloride are formed. Pass these vapours in water. A yellow
sol. of H2CrO4 is formed. Add to this solution NaOH, acetic acid and lead acetate, a yellow ppt.
confirms chloride in the mixture.
54. What is the chemistry of carbon disulphide test for a bromide or iodide?
Ans. To a part of the soda extract add dil. HCl. Now to this add small amount of CS2 and excess of
chlorine water and shake the solution well. Chlorine displaces bromine or iodine from the bromide
or iodide, which dissolves in carbon disulphide to produce orange or violet colouration.
2KBr + Cl2 ⎯→ 2KCl + Br2
2KI + Cl2 ⎯→ 2KCl + I2.
55. Why do bromides and iodides not respond to chromyl chloride test?
Ans. Because chromyl bromide (CrO2Br2) and chromyl iodide (CrO2I2) compounds are not formed,
instead of these bromine and iodine are evolved.
K2Cr2O7 + 6KI + 7H2SO4 ⎯→ 3I2 + Cr2(SO4)3 + 4K2SO4 + 7H2O
K2Cr2O7 + 6KBr + 7H2SO4 ⎯→ 3Br2 + Cr2(SO4)3 + 4K2SO4 + 7H2O.
56. Describe the chemistry of match stick test.
Ans. In match stick test, the sulphate is reduced to sulphide by carbon of match stick which then
gives violet colour with sodium nitroprusside solution.
ZnSO4 + Na2CO3 ⎯→ ZnCO3 + Na2SO4
Na2SO4 + 4C ⎯→ Na2S + 4CO
(Match
stick)
Na2S + Na2[Fe(CN)5NO] ⎯→ Na4[Fe(CN)5NOS]
Purple colour
57. Why does iodine give a blue colour with starch solution?
Ans. The blue colour is due to the formation of a complex between iodine and starch.
58. Why is original not prepared in conc. HNO3?
Ans. HNO3 is an oxidising agent which on decomposition gives oxygen. A yellow ppt. of sulphur is
obtained in presence of HNO3 when H2S is passed.
H2S + 2HNO3 ⎯→ 2NO2 + 2H2O + S.
59. Name group reagents for different groups.
Ans. Group I—Dil. HCl.
Group II—H2S in the presence of dil. HCl.
Group III—NH4OH in the presence of NH4Cl.
Group IV—H2S in the presence of NH4OH.
Group V—(NH4)2 CO3 in the presence of NH4Cl and NH4OH.
Group VI—No specific group reagent.
198 COMPREHENSIVE PRACTICAL CHEMISTRY—XII
60. Why is it essential to add dil. HCl before proceeding to the test for the basic radicals of
group II?
Ans. Dilute HCl increases the concentration of H+ ions in the solution and hence suppresses the
dissociation of H2S due to common ion effect. As a result of which the sulphide ion concentration is
sufficient only to exceed the solubility products of the sulphides of group II cations.
Since the solubility products (Ksp) for the sulphides of groups III and IV cations are very high,
those cations are not precipitated under the above conditions.
61. Why is the O.S. boiled with conc. HNO3 in group III?
Ans. In the presence of NH4Cl, Fe(OH)2 is not completely precipitated because of its high solubility
product. For this reason Fe2+ salts are oxidised to Fe3+ salts by boiling with conc. HNO3 before
adding NH4Cl and NH4OH; otherwise Fe2+ would not be completely precipitated in III group.
62. Why is NH4Cl added along with NH4OH in group III?
Ans. It is done in order to decrease the concentration of OH– ions by suppressing the ionisation of
NH4OH by common ion effect. If NH4OH alone is used in that case, the concentration of OH– is
large enough to ppt. the hydroxide of IV, V and VI cations.
63. What is blue lake?
Ans. It is blue particles (blue litmus adsorbed on white ppt. of Al(OH)3 floating in colourless solution.
64. H2S gas is passed in presence of NH4OH in group IV. Explain why?
Ans. When H2S gas is passed in alkaline medium or NH4OH, the H+ ions from the dissociation of
H2S gas combine with hydroxyl ions (OH–) from the dissociation of NH4OH to form nearly union-
ised H2O.
H2S 2H+ + S2–
2NH4OH 2OH– + 2NH4+
H+ + OH– H2O
The removal of H+ ions from the solution causes more of H2S to dissociate, thereby increasing the
concentration of S2– ions to such an extent that the ionic product of IV group metal sulphides
exceeds their solubility product. Hence they are precipitated.
65. Presence of NH4Cl is quite essential before the addition of (NH4)2 CO3 in group V. Explain
why?
Ans. Ammonium chloride suppresses the ionisation of NH4OH and (NH4)2CO3 due to common ion
effect which results in the decrease in the concentration of OH– and CO32– ions. So the ionic product
does not exceed the solubility product of Mg(OH)2 or MgCO3 and thereby they are not precipitated
during analysis of group V cations.
66. Na2CO3 cannot be used in place of (NH4)2 CO3 in the group V. Explain why?
Ans. Na2CO3 is highly ionised electrolyte, which produces very high conc. of CO32– ions. As a result
ionic product of MgCO3 may exceed its Ksp and it may get precipitated along with the radicals
of V group.
67. An aqueous solution of HCl has conc. 10–8 M. What is the approximate value of pH of this
solution?
Ans. Slightly less than 7.
68. How will you prepare chlorine water?
Ans. Take conc. HCl in a test tube and add KMnO4 solution dropwise till the pink colour starts
persisting. Now add a few drops of conc. HCl so that pink colour disappears. The colourless solution
thus obtained is chlorine water.
69. Can we use ammonium sulphate in place of ammonium chloride in precipitation of
group III cations?
Ans. No, ammonium sulphate cannot be used because it would cause precipitation of group V
radicals as their sulphates during analysis of group III.
70. Name a cation which is not obtained from a metal?
Ans. Ammonium ion (NH4+).