Viva Questions Class 12
Viva Questions Class 12
Viva Questions Class 12
The substance whose standard solution can be prepared directly by weight is known as
primary, standard substance. The substance whose standard solution can’t be prepared
directly by weighing but by titration with primary standard solution are secondary
standard substance.
4) Why the last drop of solution must not be blown out of a pipette?
Answer. Since the drops left in the jet end is extra of the volume measured by the
pipette.
7) What is permanganometry ?
Answer. Redox titrations involving KMnO4 as the oxidising agent are called
permanganometric titrations.
12) Why is Mohr’s salt preferred as a primary standard over ferrous sulphate in
volumetric
analysis ?
Answer. This is because of the fact that Mohr’s salt is stable and is not readily oxidised
by air. Ferrous sulphate gets oxidised to ferric sulphate.
13) Why are a few drops of dilute sulphuric acid added while preparing a standard
solution of Mohr’s salt ?
Answer. Few drops of H2SO4 are added to prevent the hydrolysis of ferrous sulphate.
15) Why should you heat the oxalic acid solution to about 60-70°C before titrating with
KMnO4 solution ?
Answer. In cold, the reaction is very slow due to the slow formation of Mn 2+ ions. Oxalic
acid is heated to speed up the liberation of Mn 2+ ions which then autocatalyses the
reaction and thus the reaction proceeds rapidly. This also serves the purpose of
expelling the carbondioxide evolved during the reaction which otherwise does not allow
the reaction to go to completion.
Its general structure is having two polymorphs and due to this, it appears as a white
crystalline solid. After dissolving into water, it becomes a colourless solution. It is
popularly useful as the reducing agent. It works as the chelating agent with oxalate as
its conjugate base.
SALT ANALYSIS
1) What is the difference between a qualitative and quantitative analysis?
Answer. The primary distinction between qualitative analysis and quantitative analysis
in chemistry is that qualitative chemistry determines the presence or absence of various
chemical components in a sample, whereas quantitative chemistry determines the
amount of various chemical components present in a given sample.
Q2. Can we use a glass rod instead of platinum wire for performing the flame test?
Explain your answer.
Answer. No, we cannot use a glass rod instead of platinum wire for performing the
flame test. This is because platinum is unreactive and does not produce a colour in the
flame that masks the presence of other metals.
Q3. Why is platinum metal preferred to other metals for the flame test?
Answer. Platinum is chemically inert, which means it does not react with other elements
to form oxides or other compounds. When performing a flame test, this stability is
desirable because it ensures that we only see the spectrum of what we are burning.
4) Which colour of the flame is observed through the naked eye for Ca 2+?
5) Analysis of which group cation gives white fumes in the confirmatory test? Zero
group cation NH4+.
Answer. Ammonia gas produced by the action of sodium hydroxide on ammonium salts
reacts with hydrochloric acid to produce ammonium chloride, which appears as a dense
white fume.
Answer. Nessler’s reagent is a solution of mercury (II) iodide (HgI 2) in potassium iodide
(KI) and potassium hydroxide (KOH). As a confirmatory test for ammonium ion NH 4+,
Nessler’s reagent is used.
The presence of NH4+ ion is confirmed by the presence of brown or yellow precipitate.
Answer. The reddish-brown precipitate (ferric chloride- FeCl3) is formed when ferric
hydroxide is dissolved in HCl
Answer. CO2+, Ni2+, Mn2+, and Zn2+ are the radicals found in this group. On passing H 2S
gas through the salt’s ammonical solution, these are precipitated as sulphides. Thus,
the group’s reagent is H2S gas in the presence of NH4Cl and NH4OH.
Answer. If group-III is not present, pass H2S gas through the group-III solution for a
few minutes. If a precipitate (white, black, or flesh-coloured) appears, it indicates the
presence of group-IV cations.
12) Why is the original solution for cations not prepared in conc. HNO 3 or H2SO4?
Answer. Since concentrated HNO3 acid is a very strong oxidising and nitrating agent,
the original solution is not prepared in it. When nitric acid is used for salt analysis, the
conc. HNO3 in the solution can oxidise the ions present.
Concentrated H2SO4 has dehydrating properties, it can be used not only as an acid but
also as a dehydrating agent in the synthesis of other acids.
13) Why cannot conc. HCl is used as a group reagent in place of dil. HCl for the
precipitation of Ist group cations?
Answer. The conc. HCl is Not used because high concentrations of ions increase the
solubility of group I chloride precipitate through the formation of soluble complex ions.
14) How can one prevent the precipitation of Group–IV radicals, with the second group
radicals?
Answer. In the presence of HCl, H2S is passed in the qualitative analysis of cations from
the second group. The ionisation of H2S decreases and lessens as a result of the
common ion effect.
15) Can we use ammonium sulphate instead of ammonium chloride in the group–III?
16) Why is NH4OH added before (NH44)2CO3 solution while precipitating group–V
cations?
18) Why are the group–V radicals tested in the order Ba 2+, Sr2+ and Ca2+?
Answer. Ba2+ also gives Sr2+ and Ca2+ tests. Sr2+ also provides Ca2+ tests. Therefore,
before confirming Sr2+, we must demonstrate the absence of Ba2+, and before
confirming Ca2+, we must demonstrate the absence of both Ba2+ and Sr2+.
19) Why should the solution be concentrated before proceeding to the group–V?
Answer. The common ion effect describes the effect on equilibrium that occurs when a
common ion (an ion already present in the solution) is added to it. In general, the
common ion effect reduces a solute’s solubility. It can also have an effect on buffering
solutions, as adding more conjugate ions can cause the pH of the solution to change.