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NEET • CHEMISTRY • PRACTICAL CHEMISTRY

Practical chemistry practice · Medium

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31 Medium
Understanding +4 | -1
Which of the following statements are correct?

A. Glycerol is purified by vacuum distillation because it decomposes at its normal boiling point.

B. Aniline can be purified by steam distillation as aniline is miscible in water.

C. Ethanol can be separated from ethanol water mixture by azeotropic distillation because it forms azeotrope.

D. An organic compound is pure, if mixed M.P. is remained same.

Choose the most appropriate answer from the options given below :
View answer and explanation
Correct option: B
A, C, D only
The correct answer is B (A, C, D only) because glycerol is purified by vacuum distillation, ethanol can be separated by azeotropic distillation, a pure organic compound has the same mixed melting point, but aniline is miscible with water and cannot be purified by steam distillation.
Solution approach
  1. Correct Answer + Core Reason: A, C, D only. Glycerol is purified by vacuum distillation, ethanol can be separated by azeotropic distillation, and a pure organic compound has the same mixed melting point. Aniline is not purified by steam distillation as it is miscible in water.

    Step-by-Step Solution:

    Step 1: Statement A is correct: Glycerol decomposes at its normal boiling point, so vacuum distillation is used to lower the boiling point and prevent decomposition.

    Step 2: Statement B is incorrect: Aniline is miscible with water, so it cannot be purified by steam distillation. Steam distillation is used for immiscible liquids.

    Step 3: Statement C is correct: Ethanol and water form an azeotrope, which can be separated by azeotropic distillation using a third component.

    Step 4: Statement D is correct: A pure organic compound will have a sharp melting point, and the mixed melting point with an authentic sample will remain the same.

    Why other options are wrong:
    - Option A (A, B, C only): Includes incorrect statement B.
    - Option C (B, C, D only): Includes incorrect statement B.
    - Option D (A, B, D only): Includes incorrect statement B.

    Key Concepts:
    - Vacuum distillation
    - Steam distillation
    - Azeotropic distillation
    - Melting point

    Memory Aids:
    - Vacuum for decomposition, Azeotrope for mixtures

    Quick Tips:
    - Remember the principles behind different purification techniques and their applicability.
32 Medium
Remembering +4 | -1
A mixture, on heating with conc. H2SO4\mathrm{H}_2 \mathrm{SO}_4 and MnO2\mathrm{MnO}_2, librates brown vapour of
View answer and explanation
Correct option: A
Br2\mathrm{Br}_2
Option A (Br2\mathrm{Br}_2) is correct because the reaction of a mixture with conc. H2SO4 and MnO2 liberates brown vapors of bromine.
Solution approach
  1. Correct Answer + Core Reason: Br2\mathrm{Br}_2. The reaction of a mixture with conc. H2SO4H_2SO_4 and MnO2MnO_2 liberates brown vapors of bromine.

    Step-by-Step Solution:

    Step 1: Understand the Reaction: The reaction involves the oxidation of bromide ions to bromine by manganese dioxide in the presence of concentrated sulfuric acid.

    Step 2: Reaction Equation:
    2NaBr+MnO2+3H2SO4→MnSO4+2NaHSO4+Br2+2H2O2NaBr + MnO_2 + 3H_2SO_4 \rightarrow MnSO_4 + 2NaHSO_4 + Br_2 + 2H_2O

    Step 3: Properties of Bromine: Bromine (Br2Br_2) is a reddish-brown liquid that forms brown vapors.

    Step 4: Conclusion: The brown vapors are of bromine (Br2Br_2).

    Why other options are wrong:
    - Option B: NO2\mathrm{NO}_2 is a reddish-brown gas, but it's produced from nitrates, not bromides, under these conditions.
    - Option C: HBr\mathrm{HBr} is a colorless gas, not a brown vapor.
    - Option D: I2\mathrm{I}_2 is a violet vapor, not a brown vapor.

    Key Concepts:
    - Oxidation of Halide Ions
    - Reactions with MnO2MnO_2 and H2SO4H_2SO_4

    Memory Aids:
    - Bromine (Br2Br_2) is brown.

    Quick Tips:
    - Remember the characteristic colors of halogens.
33 Medium
Application +4 | -1
The pH range where the indicator shows change in colour are given as

(i) 4−9.74-9.7 \quad (ii) 7.46−10.07.46-10.0 \quad (iii) 6.5−46.5-4

Which of the above pH range represents titration of

I. Strong acid/strong base (SA/SB)\left(S_A / S_B\right)

II. Weak acid/strong base (WA/SB)\left(W_A / S_B\right)

III. Weak base/strong acid (WB/SA)\left(W_B / S_A\right)
View answer and explanation
Correct option: A
(i) →\rightarrow I, (ii) →\rightarrow II, (iii) →\rightarrow III
Option A is correct because it correctly matches the pH ranges with the respective titrations based on the strength of the acid and base involved.
Solution approach
  1. Correct Answer + Core Reason: (i) →\rightarrow I, (ii) →\rightarrow II, (iii) →\rightarrow III. The pH range depends on the strength of the acid and base in the titration.

    Step-by-Step Solution:

    Step 1: Understand the pH range for different titrations.

    Step 2: Strong acid/strong base titration has a pH range around 7 (4-9.7 is acceptable due to indicator variations).

    Step 3: Weak acid/strong base titration has a pH range above 7 (7.46-10.0 is appropriate).

    Step 4: Weak base/strong acid titration has a pH range below 7 (6.5-4 is appropriate).

    Step 5: Match the pH ranges to the corresponding titrations.

    Why other options are wrong:
    - Option B: Incorrectly assigns pH ranges to titrations.
    - Option C: Incorrectly assigns pH ranges to titrations.
    - Option D: Incorrectly assigns pH ranges to titrations.

    Key Concepts:
    - Acid-base titrations
    - pH ranges of indicators
    - Strong vs. weak acids and bases

    Memory Aids:
    - Strong acid/strong base: pH ~ 7
    - Weak acid/strong base: pH > 7
    - Weak base/strong acid: pH < 7

    Quick Tips:
    - Remember the general pH range for each type of titration.
34 Medium
Remembering +4 | -1
In qualitative test for identification of presence of phosphorous, the compound is heated with an oxidising agent. Which is further treated with nitric acid and ammonium molybdate respectively. The yellow coloured precipitate obtained is:
View answer and explanation
Correct option: C
(NH4)3PO4⋅12MoO3\left(\mathrm{NH}_4\right)_3 \mathrm{PO}_4 \cdot 12 \mathrm{MoO}_3
Option C is correct because the yellow precipitate formed in the test for phosphorus is ammonium phosphomolybdate, which has the formula (NH₄)₃PO₄ ⋅ 12MoO₃.
Solution approach
  1. Correct Answer + Core Reason: (NH4)3PO4⋅12MoO3\left(\mathrm{NH}_4\right)_3 \mathrm{PO}_4 \cdot 12 \mathrm{MoO}_3. The yellow precipitate formed is ammonium phosphomolybdate.

    Step-by-Step Solution:

    Step 1: The compound containing phosphorus is oxidized to phosphate (PO43−\mathrm{PO}_4^{3-}).

    Step 2: The phosphate ion reacts with ammonium molybdate in the presence of nitric acid to form ammonium phosphomolybdate, a yellow precipitate.

    Step 3: The balanced equation for the formation of the precipitate is:
    H3PO4+12(NH4)2MoO4+21HNO3→(NH4)3PO4⋅12MoO3+21NH4NO3+12H2O\mathrm{H}_3\mathrm{PO}_4 + 12(\mathrm{NH}_4)_2\mathrm{MoO}_4 + 21\mathrm{HNO}_3 \rightarrow (\mathrm{NH}_4)_3\mathrm{PO}_4 \cdot 12\mathrm{MoO}_3 + 21\mathrm{NH}_4\mathrm{NO}_3 + 12\mathrm{H}_2\mathrm{O}

    Step 4: The yellow precipitate is ammonium phosphomolybdate, (NH4)3PO4⋅12MoO3(\mathrm{NH}_4)_3\mathrm{PO}_4 \cdot 12\mathrm{MoO}_3.

    Why other options are wrong:
    - Option A: Na3PO4⋅12MoO3\mathrm{Na}_3 \mathrm{PO}_4 \cdot 12 \mathrm{MoO}_3: This is incorrect because the precipitate formed involves ammonium molybdate, not sodium molybdate.
    - Option B: (NH4)3PO4⋅12(NH4)2MoO4\left(\mathrm{NH}_4\right)_3 \mathrm{PO}_4 \cdot 12\left(\mathrm{NH}_4\right)_2 \mathrm{MoO}_4: This formula is incorrect as it includes additional ammonium molybdate molecules that are not part of the actual precipitate.
    - Option D: MoPO4⋅21NH4NO3\mathrm{MoPO}_4 \cdot 21 \mathrm{NH}_4 \mathrm{NO}_3: This formula is incorrect as it does not represent the correct composition of ammonium phosphomolybdate.

    Key Concepts:
    - Qualitative analysis of phosphorus
    - Formation of ammonium phosphomolybdate precipitate
    - Chemical reactions of phosphate ions

    Memory Aids:
    - Remember that the yellow precipitate is ammonium phosphomolybdate: (NH₄)₃PO₄ ⋅ 12MoO₃

    Quick Tips:
    - In qualitative analysis questions, knowing the correct formulas of precipitates is crucial. Pay attention to the reactants and the conditions of the reaction.
35 Medium
Remembering +4 | -1
K4[Fe(CN)6]\text{K}_4\left[\mathrm{Fe}(\mathrm{CN})_6\right] is not used for the detection of
View answer and explanation
Correct option: A
Fe2+\mathrm{Fe}^{2+} ions
Option A (Fe2+\mathrm{Fe}^{2+} ions) is correct because K4[Fe(CN)6]\text{K}_4\left[\mathrm{Fe}(\mathrm{CN})_6\right] reacts with Fe3+\mathrm{Fe}^{3+} to form Prussian blue, with Zn2+\mathrm{Zn}^{2+} to form a white precipitate, and with Cu2+\mathrm{Cu}^{2+} to form a chocolate-brown precipitate, but it does not form a distinctive precipitate with Fe2+\mathrm{Fe}^{2+}.
Solution approach
  1. Correct Answer + Core Reason: Fe2+\mathrm{Fe}^{2+} ions. K4[Fe(CN)6]\text{K}_4\left[\mathrm{Fe}(\mathrm{CN})_6\right] does not form a distinctive precipitate with Fe2+\mathrm{Fe}^{2+} ions.

    Step-by-Step Solution:

    Step 1: Consider the reactions of K4[Fe(CN)6]\text{K}_4\left[\mathrm{Fe}(\mathrm{CN})_6\right] with each of the given ions.

    Step 2: K4[Fe(CN)6]\text{K}_4\left[\mathrm{Fe}(\mathrm{CN})_6\right] reacts with Fe3+\mathrm{Fe}^{3+} ions to form Prussian blue, Fe4[Fe(CN)6]3\mathrm{Fe}_4[\mathrm{Fe}(\mathrm{CN})_6]_3.

    Step 3: K4[Fe(CN)6]\text{K}_4\left[\mathrm{Fe}(\mathrm{CN})_6\right] reacts with Zn2+\mathrm{Zn}^{2+} ions to form a white precipitate of K2Zn3[Fe(CN)6]2\mathrm{K}_2\mathrm{Zn}_3[\mathrm{Fe}(\mathrm{CN})_6]_2.

    Step 4: K4[Fe(CN)6]\text{K}_4\left[\mathrm{Fe}(\mathrm{CN})_6\right] reacts with Cu2+\mathrm{Cu}^{2+} ions to form a chocolate-brown precipitate of Cu2[Fe(CN)6]\mathrm{Cu}_2[\mathrm{Fe}(\mathrm{CN})_6].

    Step 5: K4[Fe(CN)6]\text{K}_4\left[\mathrm{Fe}(\mathrm{CN})_6\right] reacts with Fe2+\mathrm{Fe}^{2+} to form a light blue precipitate, but this is not a reliable test because it is easily oxidized to Prussian blue.

    Why other options are wrong:
    - Option B: Zn2+\mathrm{Zn}^{2+} ions form a white precipitate with K4[Fe(CN)6]\text{K}_4\left[\mathrm{Fe}(\mathrm{CN})_6\right].
    - Option C: Cu2+\mathrm{Cu}^{2+} ions form a chocolate-brown precipitate with K4[Fe(CN)6]\text{K}_4\left[\mathrm{Fe}(\mathrm{CN})_6\right].
    - Option D: Fe3+\mathrm{Fe}^{3+} ions form Prussian blue with K4[Fe(CN)6]\text{K}_4\left[\mathrm{Fe}(\mathrm{CN})_6\right].

    Key Concepts:
    - Qualitative analysis
    - Complex formation

    Memory Aids:
    - Remember the colors of the precipitates formed with different metal ions.

    Quick Tips:
    - Know the characteristic reactions of common metal ions with various reagents.
36 Medium
Analyzing +4 | -1
A metal salt solution forms a yellow ppt with potassium chromate in acetic acid, a white ppt with dilute sulphuric acid, but gives no ppt with sodium chloride or iodide, it is:
View answer and explanation
Correct option: C
Barium carbonate
Option C (Barium carbonate) is correct because barium ions form a yellow precipitate with potassium chromate, a white precipitate with dilute sulfuric acid, and do not precipitate with chloride or iodide ions.
Solution approach
  1. Correct Answer + Core Reason: Barium carbonate. Barium ions give the described reactions.

    Step-by-Step Solution:

    Step 1: Analyze the given reactions.

    Step 2: Yellow precipitate with potassium chromate in acetic acid suggests the formation of barium chromate (BaCrO4{BaCrO}_4).

    Step 3: White precipitate with dilute sulfuric acid suggests the formation of barium sulfate (BaSO4{BaSO}_4).

    Step 4: No precipitate with sodium chloride or iodide rules out lead (Pb2+{Pb}^{2+}) and silver (Ag+{Ag}^{+}) as they form insoluble chlorides and iodides.

    Step 5: Barium (Ba2+{Ba}^{2+}) forms insoluble chromate and sulfate but soluble chloride and iodide.

    Why other options are wrong:
    - Option A: Lead carbonate is wrong because lead forms insoluble chlorides and iodides.
    - Option B: Basic lead carbonate is wrong because lead forms insoluble chlorides and iodides.
    - Option D: Strontium carbonate is wrong because strontium chromate is not as insoluble as barium chromate, and strontium sulfate is more soluble than barium sulfate.

    Key Concepts:
    - Solubility rules
    - Precipitation reactions
    - Qualitative analysis

    Memory Aids:
    - Remember the characteristic precipitates of barium.

    Quick Tips:
    - Consider the solubility rules for chromates, sulfates, chlorides, and iodides.
37 Medium
Remembering +4 | -1
When a mixture of solid NaCl,{NaCl}, solid K2Cr2O7{K}_2 {Cr}_2 {O}_7 is heated with conc. H2SO4,{H}_2 {SO}_4, orange red vapours are obtained. These are of the compound:
View answer and explanation
Correct option: B
Chromyl chloride
Option B (Chromyl chloride) is correct because the reaction of solid NaCl and solid K2Cr2O7 with conc. H2SO4 produces chromyl chloride vapors.
Solution approach
  1. Correct Answer + Core Reason: Chromyl chloride. The reaction of solid NaCl and solid K2Cr2O7K_2Cr_2O_7 with conc. H2SO4H_2SO_4 produces chromyl chloride vapors.

    Step-by-Step Solution:

    Step 1: Understand the Reaction: The reaction involves the formation of chromyl chloride (CrO2Cl2CrO_2Cl_2) when a chloride salt is heated with potassium dichromate and concentrated sulfuric acid.

    Step 2: Reaction Equation:
    K2Cr2O7+4NaCl+6H2SO4→2CrO2Cl2+2KHSO4+4NaHSO4+3H2OK_2Cr_2O_7 + 4NaCl + 6H_2SO_4 \rightarrow 2CrO_2Cl_2 + 2KHSO_4 + 4NaHSO_4 + 3H_2O

    Step 3: Properties of Chromyl Chloride: Chromyl chloride is a volatile, orange-red liquid.

    Step 4: Conclusion: The orange-red vapors are of chromyl chloride (CrO2Cl2CrO_2Cl_2).

    Why other options are wrong:
    - Option A: Chromous chloride is not formed in this reaction.
    - Option C: Chromic chloride is not formed as a vapor in this reaction.
    - Option D: Chromic sulphate is not formed as a vapor in this reaction.

    Key Concepts:
    - Chromyl Chloride Test
    - Qualitative Analysis of Chloride Ions

    Memory Aids:
    - Chromyl chloride (CrO2Cl2CrO_2Cl_2) is orange-red.

    Quick Tips:
    - Remember the chromyl chloride test for the detection of chloride ions.
38 Medium
Remembering +4 | -1
To a metal nitrate, when KI\text{KI} solution is added, a black precipitate is produced at first, on adding excess of KI,\text{KI}, orange solution is produced. Identify the metal ion.
View answer and explanation
Correct option: A
Hg2+\mathrm{Hg}^{2+}
Option A (Hg2+\mathrm{Hg}^{2+}) is correct because mercury(II) ions react with KI to form a black precipitate that dissolves in excess KI to form a complex.
Solution approach
  1. Correct Answer + Core Reason: Hg2+\mathrm{Hg}^{2+}. Mercury(II) ions react with KI to form a black precipitate that dissolves in excess KI to form a complex.

    Step-by-Step Solution:

    Step 1: Reaction of Metal Nitrate with KI: The reaction involves the formation of a precipitate followed by the dissolution of the precipitate in excess KI.

    Step 2: Reaction with Hg2+\mathrm{Hg}^{2+}: Mercury(II) ions (Hg2+Hg^{2+}) react with KI to form a red precipitate of HgI2HgI_2 which quickly turns black. In excess KI, the HgI2HgI_2 dissolves to form a colorless complex, [HgI4]2−[HgI_4]^{2-}.
    Hg2++2KI→HgI2(red,turnsblack)↓Hg^{2+} + 2KI \rightarrow HgI_2 (red, turns black)\downarrow
    HgI2+2KI→[HgI4]2−(colorless)HgI_2 + 2KI \rightarrow [HgI_4]^{2-} (colorless)

    Step 3: Analyze the other metal ions:
    - Bi3+\mathrm{Bi}^{3+}: Forms a white precipitate with KI that does not dissolve in excess KI.
    - Cu2+\mathrm{Cu}^{2+}: Forms a brown precipitate with KI.
    - Pb2+\mathrm{Pb}^{2+}: Forms a yellow precipitate with KI that dissolves in hot water but not in excess KI.

    Step 4: Conclusion: The metal ion is Hg2+\mathrm{Hg}^{2+}.

    Why other options are wrong:
    - Option B: Bi3+\mathrm{Bi}^{3+} forms a white precipitate that does not dissolve in excess KI.
    - Option C: Cu2+\mathrm{Cu}^{2+} forms a brown precipitate with KI.
    - Option D: Pb2+\mathrm{Pb}^{2+} forms a yellow precipitate that dissolves in hot water but not in excess KI.

    Key Concepts:
    - Qualitative Analysis
    - Reactions of Metal Ions with KI
    - Complex Formation

    Memory Aids:
    - Mercury (Hg) forms a black precipitate with KI that dissolves in excess.

    Quick Tips:
    - Remember the characteristic reactions of metal ions with KI.
39 Medium
Remembering +4 | -1
Which of the following cations does not import colour to the flame in flame test?
View answer and explanation
Correct option: B
Mg2+\mathrm{Mg}^{2+}
Option B (Mg2+\mathrm{Mg}^{2+}) is correct because magnesium ions do not impart color to the flame in a flame test.
Solution approach
  1. Correct Answer + Core Reason: Mg2+\mathrm{Mg}^{2+}. Magnesium ions do not impart color to the flame.

    Step-by-Step Solution:

    Step 1: Recall the principle of the flame test.

    Step 2: Flame tests are used to identify certain metal ions based on the color they produce when heated in a flame.

    Step 3: The color is produced when electrons in the metal ions are excited to higher energy levels and then return to their ground state, emitting light of a specific wavelength.

    Step 4: Mg2+\mathrm{Mg}^{2+} does not have easily excitable electrons in the visible region.

    Why other options are wrong:
    - Option A: Ba2+\mathrm{Ba}^{2+} imparts a green color to the flame.
    - Option C: Ca2+\mathrm{Ca}^{2+} imparts a brick-red color to the flame.
    - Option D: Cu2+\mathrm{Cu}^{2+} imparts a blue-green color to the flame.

    Key Concepts:
    - Flame test
    - Atomic emission

    Memory Aids:
    - Remember the characteristic colors of common metal ions in flame tests.

    Quick Tips:
    - Know the common flame test colors for different elements.
40 Medium
Application +4 | -1
Given that the Ka(methyl orange)=4.0×10−4,K_a\text{(methyl orange)}=4.0 \times 10^{-4}, a solution at pH=2\mathrm{p H}=2 containing the indicator would be
View answer and explanation
Correct option: D
Red
Option D (Red) is correct because at pH 2, which is significantly lower than the pKa of methyl orange, the indicator will be predominantly in its acidic form, which is red.
Solution approach
  1. Correct Answer + Core Reason: Red. At pH 2, the indicator is predominantly in its acidic form, which is red.

    Step-by-Step Solution:\nStep 1: Understand the relationship between pH, pKa, and indicator color.\nStep 2: Calculate the pKa of methyl orange.\nStep 3: Determine the predominant form of the indicator at pH 2.

    Ka=4.0×10−4K_a = 4.0 \times 10^{-4}
    pKa=−log(Ka)=−log(4.0×10−4)=3.4pK_a = -log(K_a) = -log(4.0 \times 10^{-4}) = 3.4\nSince the pH (2) is much lower than the pKa (3.4), the indicator will be predominantly in its acidic form (HInd), which is red.

    Why other options are wrong:
    - Option A: Orange: This would be the color near the equivalence point.
    - Option B: Yellow: This is the color of the basic form of the indicator.
    - Option C: Colourless: Methyl orange is not colorless in either its acidic or basic form.

    Key Concepts:
    - Acid-base indicators
    - pH and pKa

    Memory Aids:
    - Remember that indicators change color near their pKa.

    Quick Tips:
    - Use the Henderson-Hasselbalch equation to determine the ratio of the acidic and basic forms of the indicator.
41 Medium
Application +4 | -1
Which of the following will be precipitated when dil. HClHCl is added to their solution.
View answer and explanation
Correct option: A
Pb(NO3)2{Pb}\left({NO}_3\right)_2
Option A (Pb(NO3)2{Pb}({NO}_3)_2) is correct because lead chloride (PbCl2PbCl_2) is insoluble in cold dilute HCl and will precipitate out.
Solution approach
  1. Correct Answer + Core Reason: Pb(NO3)2{Pb}({NO}_3)_2. Lead chloride (PbCl2PbCl_2) is insoluble in cold dilute HCl.

    Step-by-Step Solution:\nStep 1: Consider the solubility rules for chlorides.\nStep 2: Determine which metal chloride is insoluble in dilute HCl.
    \nLead chloride (PbCl2PbCl_2) is insoluble in cold water and dilute HCl. When dilute HCl is added to a solution of lead nitrate, lead chloride precipitates out.
    Pb(NO3)2(aq)+2HCl(aq)→PbCl2(s)+2HNO3(aq)Pb(NO_3)_2(aq) + 2HCl(aq) \rightarrow PbCl_2(s) + 2HNO_3(aq)

    Why other options are wrong:
    - Option B: CuSO4{CuSO}_4: Copper chloride is soluble in water.
    - Option C: MnCl2{MnCl}_2: Manganese chloride is soluble in water.
    - Option D: MgCO3{MgCO}_3: Magnesium carbonate will react with HCl to form magnesium chloride, water, and carbon dioxide, and it will dissolve.

    Key Concepts:
    - Solubility rules
    - Precipitation reactions

    Memory Aids:
    - Remember that lead chloride is insoluble.

    Quick Tips:
    - Know the solubility rules for common ionic compounds.
42 Medium
Understanding +4 | -1
Sometimes yellow turbidity appears while passing H2S\mathrm{H}_2 \mathrm{S} gas even in the absence of II group radicals. This is because of
View answer and explanation
Correct option: C
The oxidation of H2S\mathrm{H}_2 \mathrm{S} gas by some acid radicals
Option C (The oxidation of H2S\mathrm{H}_2 \mathrm{S} gas by some acid radicals) is correct because oxidizing agents present in the solution can oxidize hydrogen sulfide to elemental sulfur, causing a yellow turbidity.
Solution approach
  1. Correct Answer + Core Reason: The oxidation of H2S\mathrm{H}_2 \mathrm{S} gas by some acid radicals. Oxidizing agents oxidize H2SH_2S to elemental sulfur, causing turbidity.

    Step-by-Step Solution:
    Step 1: H2SH_2S gas is passed through a solution containing metal ions for qualitative analysis.
    Step 2: If oxidizing agents are present (e.g., Fe3+Fe^{3+}, NO3−NO_3^−), they can oxidize H2SH_2S to elemental sulfur (S).
    Step 3: The reaction is: 2H2S+O2→2S+2H2O2H_2S + O_2 \rightarrow 2S + 2H_2O (where O2O_2 represents an oxidizing agent).
    Step 4: The elemental sulfur is insoluble and forms a colloidal suspension, causing a milky or yellow turbidity.

    Why other options are wrong:
    - Option A: Sulphur is present in the mixture as impurity: While sulfur could be an impurity, the turbidity is more likely due to the oxidation of H2SH_2S.
    - Option B: IV group radicals are precipitated as sulphides: If IV group radicals were present, they would precipitate as colored sulfides, not as a yellow turbidity.
    - Option D: III group radicals are precipitated as hydroxides: III group radicals precipitate as hydroxides under basic conditions, not during the passage of H2SH_2S in acidic conditions.

    Key Concepts:
    - Oxidation-reduction reactions
    - Solubility of sulfur
    - Qualitative analysis

    Memory Aids:
    - Remember that oxidizing agents can oxidize H2SH_2S to sulfur.

    Quick Tips:
    - Consider the presence of oxidizing agents when performing sulfide precipitations.
43 Medium
Analyzing +4 | -1
A substance on treatment with dil. H2SO4\mathrm{H}_2 \mathrm{SO}_4 liberates a colourless gas which produces (i) turbidity with baryta water and (ii) turns acidified dichromate solution green. The reaction indicates the presence of
View answer and explanation
Correct option: C
SO32−\mathrm{SO}_3^{2-}
Option C is correct because sulfite ions (SO32-) react with dilute H2SO4 to release sulfur dioxide (SO2), which turns baryta water turbid and acidified dichromate solution green.
Solution approach
  1. Correct Answer + Core Reason: SO32−\mathrm{SO}_3^{2-}. The gas liberated is SO2\mathrm{SO}_2, which produces turbidity with baryta water and turns acidified dichromate green.

    Step-by-Step Solution:

    Step 1: Consider the reaction of each anion with dilute H2SO4\mathrm{H}_2\mathrm{SO}_4.

    Step 2: CO32−+H2SO4→CO2+H2O+SO42−\mathrm{CO}_3^{2-} + \mathrm{H}_2\mathrm{SO}_4 \rightarrow \mathrm{CO}_2 + \mathrm{H}_2\mathrm{O} + \mathrm{SO}_4^{2-}. CO2\mathrm{CO}_2 does not turn acidified dichromate green.

    Step 3: S2−+H2SO4→H2S+SO42−\mathrm{S}^{2-} + \mathrm{H}_2\mathrm{SO}_4 \rightarrow \mathrm{H}_2\mathrm{S} + \mathrm{SO}_4^{2-}. H2S\mathrm{H}_2\mathrm{S} turns lead acetate paper black, not dichromate green.

    Step 4: SO32−+H2SO4→SO2+H2O+SO42−\mathrm{SO}_3^{2-} + \mathrm{H}_2\mathrm{SO}_4 \rightarrow \mathrm{SO}_2 + \mathrm{H}_2\mathrm{O} + \mathrm{SO}_4^{2-}. SO2\mathrm{SO}_2 turns baryta water turbid and acidified dichromate green.

    Step 5: NO2−+H2SO4→HNO2\mathrm{NO}_2^{-} + \mathrm{H}_2\mathrm{SO}_4 \rightarrow \mathrm{HNO}_2. This reaction is more complex and doesn't directly produce a gas with the given properties.

    Step 6: Therefore, the anion is SO32−\mathrm{SO}_3^{2-}.

    Why other options are wrong:
    - Option A: CO32−\mathrm{CO}_3^{2-} produces CO2\mathrm{CO}_2, which doesn't turn dichromate green.
    - Option B: S2−\mathrm{S}^{2-} produces H2S\mathrm{H}_2\mathrm{S}, which turns lead acetate paper black.
    - Option D: NO2−\mathrm{NO}_2^{-} does not directly produce a gas with the given properties.

    Key Concepts:
    - Qualitative analysis
    - Reactions of anions with acids
    - Properties of gases like SO2\mathrm{SO}_2 and CO2\mathrm{CO}_2

    Memory Aids:
    - Remember the characteristic reactions of common anions.

    Quick Tips:
    - Consider the gases produced by each anion and their properties.
44 Medium
Analyzing +4 | -1
Given below are two statements one is labelled as Assertion (A) and the other is labeilled as Reason.

Assertion (A): In the titration of HCl against NaOH, phenolphthalein is used as suitable indicator.

Reason (R): Phenolphthalein is pink coloured in basic medium.

In the light of above statements, choose the most appropriate answer from the options given below.
View answer and explanation
Correct option: D
If both (A) and (R) are correct, but (R) is not the
correct explanation of (A)
Option D is correct because both the assertion and reason are correct, but the reason does not explain why phenolphthalein is a suitable indicator for the titration of HCl against NaOH.
Solution approach
  1. Correct Answer + Core Reason: If both (A) and (R) are correct, but (R) is not the correct explanation of (A). Phenolphthalein is suitable for strong acid-strong base titrations, and it is pink in basic medium, but the latter doesn't explain the former.

    Step-by-Step Solution:

    Step 1: Analyze the assertion: In the titration of HCl against NaOH, phenolphthalein is a suitable indicator. This is true because the pH at the equivalence point is around 7, which falls within the pH range of phenolphthalein.

    Step 2: Analyze the reason: Phenolphthalein is pink colored in basic medium. This is also true.

    Step 3: Determine if the reason explains the assertion. The fact that phenolphthalein is pink in basic medium doesn't explain why it's suitable for this specific titration. Its suitability depends on its pH range aligning with the equivalence point of the titration.

    Why other options are wrong:
    - Option A: The reason is not the correct explanation.
    - Option B: Both assertion and reason are correct.
    - Option C: Both assertion and reason are correct.

    Key Concepts:
    - Acid-base titrations
    - Acid-base indicators
    - Equivalence point
    - pH range of indicators

    Memory Aids:
    - Remember that the choice of indicator depends on the pH at the equivalence point.

    Quick Tips:
    - Consider the pH range of the indicator and the pH at the equivalence point of the titration.
45 Medium
Understanding +4 | -1
Which of the following nitrogen containing compound does not give Lassaigne's test?
View answer and explanation
Correct option: D
Hydrazine
The correct answer is D (Hydrazine) because hydrazine (N2H4N_2H_4) does not contain carbon, which is required for the Lassaigne's test to form cyanide ions.
Solution approach
  1. Correct Answer + Core Reason: Hydrazine. Hydrazine does not give Lassaigne's test because it lacks carbon.

    Step-by-Step Solution:

    Step 1: Lassaigne's test requires the organic compound to contain carbon, nitrogen, sulfur, or halogens.

    Step 2: The organic compound is fused with sodium metal to convert these elements into ionic forms.

    Step 3: For nitrogen to be detected, it must be converted to sodium cyanide (NaCNNaCN). This requires the presence of carbon in the original compound.

    Step 4: Hydrazine (N2H4N_2H_4) contains only nitrogen and hydrogen, lacking carbon. Therefore, it cannot form cyanide ions and will not give a positive Lassaigne's test for nitrogen.

    Why other options are wrong:
    - Option A (Phenyl hydrazine): Phenyl hydrazine contains carbon, nitrogen, and hydrogen and will give a positive Lassaigne's test.
    - Option B (Glycene): Glycene (Glycine) contains carbon, nitrogen, oxygen, and hydrogen and will give a positive Lassaigne's test.
    - Option C (Urea): Urea contains carbon, nitrogen, oxygen, and hydrogen and will give a positive Lassaigne's test.

    Key Concepts:
    - Lassaigne's test
    - Carbon requirement
    - Hydrazine structure

    Memory Aids:
    - No Carbon, No Lassaigne's test (for nitrogen)

    Quick Tips:
    - Remember that carbon is essential for a positive Lassaigne's test for nitrogen.
46 Medium
Understanding +4 | -1
Given below are two statements.

Statement (I) : The gas liberated on warming a salt with dil H2SO4,\mathrm{H}_2 \mathrm{SO}_4, turns a piece of paper dipped in lead acetate into black, it is a confirmatory test for sulphide ion.

Statement (II) : In statement-I the colour of paper turns black because of formation of lead sulphite.

In the light of the above statements, choose the most appropriate answer from the options given below
View answer and explanation
Correct option: B
Statement I is true but Statement II is false
Option B (Statement I is true but Statement II is false) is correct because hydrogen sulfide gas turns lead acetate paper black due to the formation of lead sulfide, not lead sulfite.
Solution approach
  1. Correct Answer + Core Reason: Statement I is true but Statement II is false. H2SH_2S reacts with lead acetate to form lead sulfide, which is black.

    Step-by-Step Solution:
    Step 1: Statement I describes the reaction of a sulfide salt with dilute H2SO4H_2SO_4 to produce H2SH_2S gas.
    Step 2: H2SH_2S gas reacts with lead acetate (Pb(CH3COO)2Pb(CH_3COO)_2) on the paper to form lead sulfide (PbSPbS).
    Step 3: The reaction is: Pb(CH3COO)2(aq)+H2S(g)→PbS(s)+2CH3COOH(aq)Pb(CH_3COO)_2(aq) + H_2S(g) \rightarrow PbS(s) + 2CH_3COOH(aq)
    Step 4: Lead sulfide (PbSPbS) is a black precipitate.
    Step 5: Statement II claims the color is due to lead sulfite, which is incorrect. The color is due to lead sulfide.

    Why other options are wrong:
    - Option A: Both Statement I and Statement II are false: Statement I is true, so this option is incorrect.
    - Option C: Both Statement I and Statement II are true: Statement II is false, so this option is incorrect.
    - Option D: Statement I is false but Statement II is true: Statement I is true, so this option is incorrect.

    Key Concepts:
    - Qualitative analysis of sulfide ions
    - Reaction of sulfides with lead acetate
    - Formation of precipitates

    Memory Aids:
    - Remember that H2SH_2S turns lead acetate paper black due to the formation of PbSPbS.

    Quick Tips:
    - Know the characteristic reactions and colors of common ions in qualitative analysis.
47 Medium
Understanding +4 | -1
While preparing crystals of Mohr's salt, dil. H2SO4\mathrm{H}_2 \mathrm{SO}_4 is added to a mixture of ferrous sulphate and ammonium sulphate, before dissolving this mixture in water, dil. H2SO4\mathrm{H}_2 \mathrm{SO}_4 is added here to:
View answer and explanation
Correct option: A
Prevent the hydrolysis of ferrous sulphate
Option A (Prevent the hydrolysis of ferrous sulphate) is correct because dilute sulfuric acid is added to prevent the hydrolysis of ferrous sulfate by maintaining a low pH.
Solution approach
  1. Correct Answer + Core Reason: Prevent the hydrolysis of ferrous sulphate. Dilute sulfuric acid prevents the hydrolysis of Fe2+Fe^{2+} ions by maintaining a low pH.

    Step-by-Step Solution:
    Step 1: Ferrous sulfate (FeSO4FeSO_4) can undergo hydrolysis in water, forming iron hydroxide and sulfuric acid: Fe2+(aq)+2H2O(l)⇌Fe(OH)2(s)+2H+(aq)Fe^{2+}(aq) + 2H_2O(l) \rightleftharpoons Fe(OH)_2(s) + 2H^+(aq)
    Step 2: The formation of iron hydroxide can lead to a precipitate and reduce the yield of Mohr's salt.
    Step 3: Adding dilute sulfuric acid (H2SO4H_2SO_4) increases the concentration of H+H^+ ions in the solution.
    Step 4: This shifts the equilibrium to the left, suppressing the hydrolysis of Fe2+Fe^{2+} ions and preventing the formation of iron hydroxide.

    Why other options are wrong:
    - Option B: Prevent the hydrolysis of ammonium sulphate: Ammonium sulfate is less prone to hydrolysis than ferrous sulfate, so this is not the primary reason.
    - Option C: Make the medium strongly acidic: While the medium becomes acidic, the main purpose is to prevent hydrolysis, not just to make it strongly acidic.
    - Option D: Increase the rate of formation of crystals: The addition of dilute sulfuric acid primarily prevents hydrolysis, not directly increasing the rate of crystal formation.

    Key Concepts:
    - Hydrolysis of metal ions
    - Le Chatelier's principle
    - Common ion effect
    - Preparation of Mohr's salt

    Memory Aids:
    - Remember that acids suppress the hydrolysis of metal ions.

    Quick Tips:
    - Understand the factors that affect the hydrolysis of metal ions.
48 Medium
Remembering +4 | -1
Disodium hydrogen phoshate is used to test:
View answer and explanation
Correct option: A
Mg2+\mathrm{Mg}^{2+}
Option A (Mg2+\mathrm{Mg}^{2+}) is correct because disodium hydrogen phosphate is used as a reagent to test for magnesium ions.
Solution approach
  1. Correct Answer + Core Reason: Mg2+\mathrm{Mg}^{2+}. Disodium hydrogen phosphate is used to test for Mg2+\mathrm{Mg}^{2+} ions.

    Step-by-Step Solution:

    Step 1: Recall the reaction of Mg2+\mathrm{Mg}^{2+} with disodium hydrogen phosphate.

    Step 2: Mg2+\mathrm{Mg}^{2+} ions react with disodium hydrogen phosphate (Na2HPO4\mathrm{Na_2HPO_4}) in the presence of ammonia to form a white precipitate of magnesium ammonium phosphate (MgNH4PO4\mathrm{MgNH_4PO_4}).

    Step 3: The formation of this precipitate indicates the presence of Mg2+\mathrm{Mg}^{2+} ions.

    Why other options are wrong:
    - Option B: Na+\mathrm{Na}^{+} does not form a precipitate with disodium hydrogen phosphate.
    - Option C: Ca2+\mathrm{Ca}^{2+} may form a precipitate with phosphate, but the test is more specific for Mg2+\mathrm{Mg}^{2+} in the presence of ammonia.
    - Option D: All - This is incorrect because the test is primarily used for Mg2+\mathrm{Mg}^{2+}.

    Key Concepts:
    - Qualitative analysis
    - Precipitation reactions

    Memory Aids:
    - Mg2+\mathrm{Mg}^{2+} + Na2HPO4\mathrm{Na_2HPO_4} + NH3\mathrm{NH_3} → MgNH4PO4\mathrm{MgNH_4PO_4} (white precipitate).

    Quick Tips:
    - Remember the specific reagents used to test for different ions.
49 Medium
Understanding +4 | -1
In copper turnings test, pieces of copper is added to a nitrate salt and heated with conc. H2SO4.\mathrm{H}_2 \mathrm{SO}_4. In this reaction copper acts as
View answer and explanation
Correct option: C
Reducing agent
Option C (Reducing agent) is correct because copper loses electrons (oxidation) to reduce nitrate ions to nitrogen dioxide.
Solution approach
  1. Correct Answer + Core Reason: Reducing agent. Copper loses electrons and reduces nitrate ions.

    Step-by-Step Solution:

    Step 1: The reaction involves copper turnings, a nitrate salt, and concentrated sulfuric acid.

    Step 2: The nitrate salt is reduced to nitrogen dioxide (NO2NO_2).

    Step 3: Copper is oxidized to copper(II) ions (Cu2+Cu^{2+}).

    Step 4: The half-reactions are:
    - Oxidation: Cu→Cu2++2e−Cu \rightarrow Cu^{2+} + 2e^-
    - Reduction: NO3−+2H++e−→NO2+H2ONO_3^- + 2H^+ + e^- \rightarrow NO_2 + H_2O

    Step 5: Since copper loses electrons, it acts as a reducing agent.

    Why other options are wrong:
    - Option A: Oxidising agent: Copper is oxidized, not reduced, so it's not an oxidizing agent.
    - Option B: Dehydrating agent: Concentrated sulfuric acid acts as a dehydrating agent, not copper.
    - Option D: Bleaching agent: Copper does not act as a bleaching agent in this reaction.

    Key Concepts:
    - Redox reactions
    - Oxidizing and reducing agents

    Memory Aids:
    - Oxidation is loss of electrons (LEO), reduction is gain of electrons (GER).

    Quick Tips:
    - Identify the oxidation states of the reactants and products to determine the oxidizing and reducing agents.
50 Medium
Application +4 | -1
At what pH will a 10−3M10^{-3} \mathrm{M} solution of indicator with Kb=10−10K_b=10^{-10} changes colour
View answer and explanation
Correct option: B
4
Option B (4) is correct because the pH at which an indicator changes color is approximately equal to its pKa_a value. Since Kb_b is given, we can calculate pKa_a and thus the pH.
Solution approach
  1. Correct Answer + Core Reason: 4. The pH at which the indicator changes color is approximately equal to its pKa_a.

    Step-by-Step Solution:

    Step 1: Understand the problem. We are given the Kb_b of an indicator and its concentration, and we need to find the pH at which it changes color.

    Step 2: Recall the relationship between Ka_a and Kb_b. We know that Ka×Kb=KwK_a \times K_b = K_w, where Kw=10−14K_w = 10^{-14}.

    Step 3: Calculate Ka_a. Ka=KwKb=10−1410−10=10−4K_a = \frac{{K_w}}{{K_b}} = \frac{{10^{-14}}}{{10^{-10}}} = 10^{-4}

    Step 4: Calculate pKa_a. pKa=−log⁡(Ka)=−log⁡(10−4)=4pK_a = -\log(K_a) = -\log(10^{-4}) = 4

    Step 5: Determine the pH. The pH at which the indicator changes color is approximately equal to its pKa_a. Therefore, pH = 4.

    Final Answer: 4

    Why other options are wrong:
    - Option A (10): This is the pKb_b value, not the pKa_a value. The indicator changes color around its pKa_a, not pKb_b.
    - Option C (3): This value is incorrect. It might be a result of miscalculating the pKa_a or misunderstanding the relationship between Ka_a, Kb_b, and pH.
    - Option D (7): This is the pH of a neutral solution. Indicators change color at different pH values depending on their Ka_a and Kb_b values.

    Key Concepts:
    - Acid-base indicators
    - Ka_a, Kb_b, and Kw_w relationship: Ka×Kb=KwK_a \times K_b = K_w
    - pKa_a and pH relationship

    Memory Aids:
    - pKa=−log⁡(Ka)pK_a = -\log(K_a)
    - pH=pKapH = pK_a at the equivalence point

    Quick Tips:
    - Remember the relationship between Ka_a, Kb_b, and Kw_w.
    - The indicator changes color at a pH close to its pKa_a.
Revision notes and key takeaways

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