Class-12-Chemistry-board-exam-questions
CLASS XII CBSE BOARD EXAM CHEMISTRY IMPORTANT QUESTIONS
CBSE Class 12 Chemistry – Chapter-wise Marks Distribution| S. No. | Title | Marks |
|---|---|---|
| 1 | Solutions | 7 |
| 2 | Electrochemistry | 9 |
| 3 | Chemical Kinetics | 7 |
| 4 | d- and f-Block Elements | 7 |
| 5 | Coordination Compounds | 7 |
| 6 | Haloalkanes and Haloarenes | 6 |
| 7 | Alcohols, Phenols and Ethers | 6 |
| 8 | Aldehydes, Ketones and Carboxylic Acids | 8 |
| 9 | Amines | 6 |
| 10 | Biomolecules | 7 |
| TOTAL | 70 | |
Question 4: What kind of attractive intermolecular interaction is present between methanol and acetone?
Question 5: Which of BaCl₂ and KCl is better at causing a negatively charged colloidal sol to coagulate? Give an explanation.
Question 6: Raoult's law deviates from non-ideal solutions either positively or negatively. What causes these deviations, and what are they? Describe each class with one example.
What is the benefit of determining the molar masses of solutes in solutions using osmotic pressure as opposed to other colliding properties?
Question 8: Give definitions for the following terms:
Question 10: Describe Henry's law and list two significant uses for it.
Question 11: Why do gases almost always become less soluble in liquids as the temperature rises?
Question 12: Below 273 K, a sodium chloride aqueous solution freezes. Using an appropriate illustration, describe how the freezing points of water are dropping.
(ii) What happens if the blood cell is submerged in a hypotonic solution of water? Give an explanation. (All India, 2015)
UNIT II Electrochemistry
Question 2: How does adding a catalyst affect
(a) Energy of activation (Ea), and
(b) A reaction's Gibbs energy (AG)?
Question 3.
Below are two electrochemical cell half-cell reactions:
MnO₄(aq) + 8H⁺(aq) + 5e⁻ → Mn²⁺(aq) + 4H₂O(l), E° = + 1.51 V Sn²⁺ (aq) → 4 Sn⁴⁺ (aq) + 2e⁻, E° = + 0.15 V
Create the redox equation using the two half-cell reactions, then determine whether the reaction favors the creation of the reactants or products indicated in the equation.
Mg2+/Mg = -2.37 V, Cr3+/Cr = -0.74 V, Fe2+/Fe = -0.44 V.
Arrange these metals in increasing order of their reducing power.
Sn2+ (aq) → Sn4+ (aq) + 2e–, E° = + 0.15 V.
Construct the redox reaction equation from the two half-reactions and calculate the cell potential from the standard potentials and predict if the reaction is reactant or product favoured.
Question 7: Two half-reactions of an electrochemical
cell are given below :
MnO–4 (aq) + 8H+ (aq) + 5e– → Mn2+ (aq) + 4H2O (I), E°
= 1.51 V
Sn2+ (aq) → Sn4+ (aq) + 2e–, E° = + 0.15 V.
Construct the redox reaction equation from the two
half-reactions and calculate the cell potential from the standard potentials
and predict if the reaction is reactant or product favoured.
Question 8: Determine the values of equilibrium
constant (Kc) and ΔG° for the following reaction:
Ni(s) + 2Ag+ (aq) → Ni2+ (aq) + 2Ag(s),
E° = 1.05 V
(1F = 96500 C mol-1)
Question 9: Two half-reactions of an electrochemical
cell are given below :
MnO₄⁻ (aq) + 8H⁺ (aq) + 5e– → Mn²⁺ (aq) + 4H₂O (I), E°
= 1.51 V
Sn²⁺ (aq) → Sn⁴⁺ (aq) + 2e⁻, E° = + 0.15 V.
Construct the redox equation from the standard
potential of the cell and predict if the reaction is reactant favored or
product favored.
Question 10: A zinc rod is dipped in 0.1 M solution of ZnSO₄. The salt is 95% dissociated at this dilution at 298 K. Calculate the
electrode potential.
[E°Zn²⁺/Zn = – 0.76 V]
Question 11: The conductivity of 0.20 M solution of
KCl at 298 K is 0.025 S cm-1. Calculate its molar conductivity. (Delhi 2013)
Question12: State Kohlrausch law of independent
migration of ions. Why does the conductivity of a solution decrease with
dilution?
Question 13: Define the following terms :
(i) Rate constant (k)
(ii) Activation energy (Ea)
Question 14: (a) following reactions occur at the cathode during the electrolysis of aqueous silver chloride solution :
Ag⁺(aq) + e– → Ag(s) E° = +0.80 V
H+(aq) + e– → 12H2(g) E° = 0.00 V
On the basis of their standard reduction electrode
potential (E°) values, which reaction is feasible at the cathode, and why?
(b) Define limiting molar conductivity. Why
conductivity of an electrolyte solution decrease with the decrease in
concentration?
Question 15: From the given cells: Lead storage cell,
Mercury cell, Fuel cell and Dry cell
Answer the following:
(i) Which cell is used in hearing aids?
(ii) Which cell was used in the Apollo Space Program?
(iii) Which cell is used in automobiles and inverters?
(iv) Which cell does not have long life?(Delhi 2016)
Question 16: Calculate the degree of dissociation (a)
of acetic acid if its molar conductivity (Λm) is 39.05 S cm2 mol-1.
Given: λ°(H+) = 349.6 S cm² mol⁻¹ and λ°(CH3COO–) =
40.9 S cm2 mol-1 (Delhi 2017)
Question 15: The Following reactions can occur at cathode
during the electrolysis of aqueous silver nitrate solution using Pt electrodes
:
On the basis of their standard electrode potential
values, which reaction is feasible at the cathode, and why?
Question 17: A
copper-silver cell is set up. The copper ion concentration in it is 0.10 M. The
concentration of silver ion is not known. The cell potential is measured at 0.422 V. Determine the concentration of silver ion in the cell.
Given : E°Ag+/Ag = + 0.80 V, E° Cu2+/Cu = + 0.34 V.
(All India 2009)
Question 18: When a certain conductance cell was
filled with 0.1 M KCl, it has a resistance of 85 ohms at 25°C. When the same
cell was filled with an aqueous solution of 0.052 M unknown electrolyte, the
resistance was 96 ohms. Calculate the molar conductance of the electrolyte at
this concentration.
[Specific conductance of 0.1 M KCl = 1.29 × 10⁻² ohm⁻¹ cm⁻¹]
Question 19: The cell in which the following reaction
occurs :
2Fe3+ (aq) + 2I⁻ (aq) → 2Fe2+ (aq) + I2 (s) has E₀ cell = 0.236V at 298K. Calculate the standard Gibbs energy and the equilibrium
constant of the cell reaction.
(Antilog of 6.5 = 3.162 × 106; of 8.0 = 10 × 108; of
8.5 = 3.162 × 108)
UNIT III CHEMICAL KINETICS
Question1: Define ‘order of a reaction’
Question 2: Define ‘activation energy’ of a reaction
Question 3: Express the rate of the following reaction
in terms of the formation of ammonia :
N2(g) + 3H2(g) → 2NH3(g)
Question 4: Write the unit of rate constant for a zero
order reaction.
Question 5: A reaction is of second order with respect
to a reactant. How will the rate of reaction be affected if the concentration
of this reactant is
(i)
doubled,
(ii) reduced to half?
Question 6: Distinguish between ‘rate expression’ and
‘rate constant’ of a reaction
Question 7: What do you understand by the rate law and
rate constant of a reaction? Identify the order of a reaction if the units of
its rate constant are : (i) L-1 mol s-1 (ii) L mol-1 s-1
Question 8: The thermal decomposition of HCO2H is a
first order reaction with a rate constant of 2.4 × 10-3 s-1 at a certain
temperature. Calculate how long will it take for three-fourths of initial
quantity of HCO2 H to decompose. (log 0.25 = -0.6021)
Question 9: A reaction is of second order with respect to a
reactant. How is the rate of reaction affected if the concentration of the
reactant is reduced to half? What is the unit of rate constant for such a
reaction? (All India 2011)
Question 10: A reaction is of second order with respect to a
reactant. How is its rate affected if the concentration of the reactant is (i)
doubled (ii) reduced to half?
Question 10: A first order gas phase reaction :
A2B2(g) → 2A(g) + 2B(g) at the temperature 400°C has the rate constant k = 2.0
× 10-4 sec-1. What percentage of A2B2 is decomposed on heating for 900 seconds?
(Antilog 0.0781 = 1.197)
Question 11: Define the following terms :
(a) Pseudo first order reaction.
(b) Half life period of reaction (t1/2).
Question 12: a) For a reaction, A + B → Product, the
rate law is given by, Rate = k[A]1[B]2. What is the order of the reaction?
(b) Write the unit of rate constant ‘k’ for the first
order reaction
Question 13: How does a change in temperature affect
the rate, of a reaction? How can this effect on the rate constant of a reaction
be represented quantitatively? (Comptt. All India 2014)
Question 14: Define each of the following :
(i) Specific rate of a reaction
(ii) Energy of activation of a reaction
Question 15: Derive integrated rate equation for rate
constant of a first order reaction
Question 16: For a decomposition reaction the values
of rate constant k at two different temperatures are given below :
k1 = 2.15 × 10-8 L mol-1 s-1 at 650 K
k2 = 2.39 × 10-7 L mol-1 s-1 at 700 K
Calculate the value of activation energy for this reaction.
(R = 8.314 J K-1 mol-1) (All India 2009)
Question 17: The rate of a reaction becomes four times when the
temperature changes from 293 K to 313 K. Calculate the energy of activation
(Ea) of the reaction assuming that it does not change with temperature. [R =
8.314 JK-1 mol-1, log 4 = 0.6021] (All India 2013)
Question 18: The rate constant for the first order decomposition of
H2O2 is given by the following equation:
log k = 14.2 – 1.0×104TK
Calculate Ea for this reaction and rate constant k if
its half-life period be 200 minutes.
(Given: R = 8.314 J K-1 mol-1) (Delhi 2016)
Question
19: Following data are
obtained for the reaction:
N2O5 → 2NO2 + 12O2
|
t/s |
0 |
300 |
600 |
|
[N205]/mol L-1 |
1.6 × 10-2 |
0.8 × 10-2 |
0.4 × 10-2 |
(a) Show that it
follows first order reaction.
(b) Calculate the half-life.
(Given log 2 = 0.3010 log 4 = 0.6021) (Delhi 2016)
Question 20: (a) With the help of a labelled diagram
explain the role of activated complex in a reaction.
(b) A first order reaction is 15% completed in 20
minutes. How long will it take to complete 60% of the reaction ? (Comptt. Delhi
2012)
UNIT IV d- and f-Block Elements
1.
What
is meant by ‘lanthanoid contraction’?
2.
Why
do transition elements show variable oxidation states?
3.
Write
the formula of an oxo-anion of Manganese (Mn) in which it shows the oxidation
state equal to its group number
4.
Write
the formula of an oxo-anion of Chromium (Cr) in which it shows the oxidation
state equal to its group number. (Delhi 2017)
5.
Explain the
following observations :
(i) Generally there is an increase in density of
elements from titanium (Z = 22) to copper (Z = 29) in the first series of
transition elements.
(ii) Transition elements and their compounds are
generally found to be good catalysts in chemical reactions. (Delhi 2010)
6.
Assign
reasons for the following :
(i) Copper (I) ion is not known in aqueous
solution.
(ii) Actinoids exhibit greater range of oxidation
states than lanthanoids
7.
How would
you account for the following :
(i) Cr2+ is reducing in nature while with the same
d-orbital configuration (d4) Mn3+ is an oxidising agent.
(ii) In a transition series of metals, the metal
which exhibits the greatest number of oxidation
states occurs in the middle of the series.
8.
State
reasons for the following :
(i) Cu (I) ion is not stable in an aqueous
solution.
(ii) Unlike Cr3+, Mn2+, Fe3+ and the subsequent other M2+ ions of the 3d series of elements, the 4d
and the 5d series metals generally do not form stable cationic species. (All
India 2011)
9.
Explain
giving a suitable reason for each of the following :
(i) Transition metals and their compounds are
generally found to be good catalysts.
(ii) Metal-metal bonding is more frequent for the
4d and the 5d series of transition metals than that for the 3d series. (All
India 2011)
10. Complete the following chemical equations :
(Delhi 2012)
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11. Explain the following :
(a) The enthalpies of atomization of transition
metals are quite high.
(b) The transition metals and many of their
compounds act as good catalysts. (Comptt. Delhi 2012)
12. What is meant by ‘disproportionation’? Give an
example of a disproportionation reaction in aqueous solution. (Comptt. Delhi
2015)
13. Describe the preparation of potassium permanganate.
How does the acidified permanganate solution react with oxalic acid? Write the
ionic equations for the reactions. (Comptt. All India 2015)
14. Describe the oxidising action of potassium
dichromate and write the ionic equations for its reaction with
(i) iodine (ii) H2S. (Comptt. All India 2015)
15. When chromite ore FeCr2O4 is fused with NaOH in presence of air, a
yellow coloured compound (A) is obtained which on acidification with dilute
sulphuric acid gives a compound (B). Compound (B) on reaction with KC1 forms an
orange coloured crystalline compound (C).
(i) Write the formulae of the compounds (A), (B)
and (C).
(ii) Write one use of compound (C). (Delhi 2016)
16. How would you account for the following :
(i) Many of the transition elements and their
compounds can act as good catalysts.
(ii) The metallic radii of the third (5d) series
of transition elements are virtually the same as those of the corresponding
members of the second series.
(iii) There is a greater range of oxidation states
among the actinoids than among the lanthanoids. (All India 2009)
17. Explain the following observations giving an
appropriate reason for each.
(i) The enthalpies of atomization of transition
elements are quite high.
(ii) There occurs much more frequent metal- metal
bonding in compounds of heavy transition metals (i.e. 3rd series).
(iii) Mn2+ is much more resistant than Fe2+ towards oxidation. (Delhi 2012)
18. Explain the following observations :
(i) Many of the transition elements are known to
form interstitial compounds
(ii) There is a general increase in density from
titanium (Z = 22) to copper (Z = 29).
(iii) The members of the actinoid series exhibit a
larger number of oxidation states than the corresponding members of the
lanthanoid series. (All India 2012)
19. Explain each of the following observations :
(i) With the same d-orbital configuration (d4), Cr2+ is a reducing agent while Mn3+ is an oxidising agent.
(ii) Actinoids exhibit a much larger number of
oxidation states than the lanthanoids.
(iii) There is hardly any increase in atomic size
with increasing atomic numbers in a series of transition metals. (All India
2012)
20. A mixed oxide of iron and chromium is fused
with sodium carbonate in free access of air to form a yellow coloured compound
(A). On acidification the compound (A) forms an orange coloured compound (B),
which is a strong oxidizing agent. Identify compound (A) and (B). Write
chemical reactions involved. (Comptt. All India 2017)
21. (a) Give reasons for the following:
(i) Compounds of transition elements are generally
coloured.
(ii) MnO is basic while Mn2O7 is acidic.
(iii) Calculate the magnetic moment of a divalent
ion in aqueous medium if its atomic number is 26. (Comptt. All India 2017)
22. (a) Why do transition elements show variable
oxidation states?
(i) Name the element showing maximum number of
oxidation states among the first series of transition metals from Se (Z = 21)
to Zn (Z = 30).
(ii) Name the element which shows only +3
oxidation state.
(b) What is lanthanoid contraction? Name an
important alloy which contains some of the lanthanoid metals. (All India 2013)
23. Give reasons :
(i) Zirconium (Z = 40) and Hafnium (Z = 72) have
almost similar atomic radii.
(ii) d-block elements exhibit more oxidation
states than f-block elements.
(iii) The enthalpies of atomization of the
transition metals are high.
(iv) The variation in oxidation states of
transition metals is of different type from that of the non-transition metals.
(v) Orange solution of potassium dichromate
24. The elements of 3d transition series are given
as:
Se Ti V Cr Mn Fe Co Ni Cu Zn
Answer the following:
(i) Write the element which shows maximum number
of oxidation states. Give reason.
(ii) Which element has the highest m.p.?
(iii) Which element shows only +3 oxidation state?
(iv) Which element is a strong oxidizing agent in
+3 oxidation state and why? (All India)
UNIT V Coordination Compounds
1. Give an example of linkage isomerism. (Delhi)
2010
2. Give IUPAC name of
ionization isomer of [Ni(NH3)3NO3]Cl. (Comptt. All India 2012)
3. Write down the formula of :
Tetraamineaquachloridocobalt(III) chloride. (Comptt. All India 2012)
4. Which complex ion is
formed when undecomposed AgBr is washed with hypo solution in photography?
(Comptt. All India 2013)
5. Give IUPAC name of the
ionization isomer of [Ni(NH3)3NO3]Cl. (Comptt. All India 2013)
6. Give two examples of
ligands which form coordination compounds useful in analytical chemistry.
(Comptt. All India 2013)
7. Which of the following
is more stable complex and why?
[Co(NH3)6]3+ and
[Co(en)3]3+ (Delhi 2014)
8. What is meant by
chelate effect? (Comptt. All India 2015)
9. Why are low spin
tetrahedral complexes not formed? (Comptt. Delhi 2017)
10. Write IUPAC name of
the complex: [CoCl2(en)2]+ (Comptt. All India 2017)
11. Name the following
coordination compounds according to IUPAC system of nomenclature :
(i) [Co(NH3)4 (H2O)Cl]Cl2
(ii) [CrCl2(en)2]Cl,
(en = ethane – 1, 2 –
diamine) (Delhi 2010)
12. Describe the shape and magnetic
behaviour of following complexes :
(i) [CO(NH3)6]3+
(ii) [Ni(CN)4]2- (At. No. Co = 27, Ni = 28) (Delhi 2010)
13. How is the stability of a co-ordination compound in solution decided
?
How is the dissociation constant of a complex
defined? (Comptt. All India 2012)
14. Explain
why [Co(NH3)6]3+ is an inner orbital complex whereas [Ni(NH3)6]2+ is an outer
orbital complex. (At. no. Co = 27, Ni = 28) (Comptt. All India 2013)
15. When a co-ordination compound CrCl3.6H2O is mixed with AgNO3, 2
moles of AgCl are precipitated per mole of the compound. Write
(i) Structural formula of the complex.
(ii) IUPAC name of the complex. (Delhi 2016)
16. Using
IUPAC norms write the formulae for the following:
(i) Sodium dicyanidoaurate (I)
17. For the complex [Fe(en)2Cl2], Cl, (en = ethylene diamine), identify
(i) the oxidation number of iron,
(ii) the hybrid orbitals and the shape of the
complex,
(iii) the magnetic behaviour of the complex,
(iv) the number of geometrical isomers,
(v) whether there is an optical isomer also, and
(vi) name of the complex. (At. no. of Fe = 26)
(Delhi 2009)
18. Compare the following complexes with respect to their shape,
magnetic behaviour and the hybrid orbitals involved :
(i) [CoF4]2-
(ii) [Cr(H2O)2(C2O4)2]–
(iii) [Ni(CO)4] (Atomic number : Co = 27, Cr = 24, Ni = 28)
(Delhi 2009)
19. Giving a suitable example for each, explain the following :
(i) Crystal field splitting
(ii) Linkage isomerism
(iii) Ambidentate ligand (All India 2009)
20. Explain the following :
(i) Low spin octahedral complexes of nickel are
not known.
(ii) The π-complexes are known for transition
elements only.
(iii) CO is a stronger ligand than NTL, for many
metals. (All India 2009)
21. Explain the following cases giving appropriate reasons :
(i) Nickel does not form low spin octahedral
complexes.
(ii) The n-complexes are known for the transition
metals only. (All India 2010)
21. Explain the following terms giving a suitable example in each case :
(i) Ambident ligand
(ii) Denticity of a ligand
(iii) Crystal field splitting in an octahedral
field
22. State a reason for each of the following situations :
(i) Co2+ is easily oxidized to Co3+ in presence of a strong ligand.
(ii) CO is a stronger complexing reagent than NH3.
(iii) The molecular shape of [Ni(CO)4] is not the
same as that of [Ni(CN)4]2- (Delhi 2011)
23. Write the name, the structure and the magnetic behaviour of each one
of the following complexes :
(i) [Pt(NH3)2Cl(NO2)]
(ii) [Co(NH3)4Cl2]Cl
(iii) Ni(CO)4 (Atmos. Co = 27, Ni = 28, Pt = 78) (Delhi
2011)
24. (a) Give
two examples of coordination compounds used in industries.
(b) Using valence bond theory, explain the geometry and magnetic
behaviour of [Co(NH3)6]3+
(At. no. of Co = 27) (Comptt. Delhi 2011)
25. What is meant by crystal field splitting energy? On the basis of
crystal field theory, write the electronic configuration of d4 in terms of t2g and eg in an octahedral field when
(i) Δ0 > P
(ii) Δ0 < P (All India 2013)
26. (a) How is a double salt different from a complex?
(b) Write IUPAC names of the following :
(i) K3[Fe(C2O4)3]
(ii) [Pt(NH3)6]Cl4.
(c) Draw the structure of cis isomer of [CO(NH3)4Cl2]+ (Comptt. Delhi 2013)
27. (a) For the complex [Fe(H2O)6]3+, write the hybridization, magnetic character and
spin of the complex. (At. number: Fe = 26)
(b) Draw one of the geometrical isomers of the
complex [Pt(en)2Cl2]2+ which is optically inactive. (All India 2016)
28. (a) What type of isomerism is shown by the complex [Co(NH3)5 (SCN)]2+?
(b) Why is [NiCl24]2- paramagnetic while [Ni(CN)4]2- is diamagnetic? (Atomic number of Ni = 28)
(c) Why are low spin tetrahedral complexes rarely
observed? (All India 2017)
UNIT VI Haloalkanes and Haloarenes
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Unit 7-8 Download here
UNIT 8 AMINES
(i) Ethyl amine and Aniline
(ii) Aniline and Benzylamine (All India 2010)
9. Give the chemical tests to distinguish between the following pairs of compounds :
(i) Methylamine and Dimethylamine
(ii) Aniline and N-methylaniline (All India 2010)
(i) Carbylamine reaction
(ii) Hofmann’s bromamide reaction (All India 2012)
(a) Aniline to p-hydroxyazobenzene
(b) Ethanoyl chloride to Ethanenitrile. (Comptt. Delhi 2012)
(a) Aniline is a weaker base than cyclohexyl amine.
(b) Methylamine in aqueous medium gives reddish-brown precipitate with FeCl3. (Comptt. All India 2012)
(a) Electrophilic susbstitution in case of aromatic amines takes place more readily than benzene.
(b) Ethanamide is a weaker base than ethanamine. (Comptt. All India 2012)
(a) Sandmeyer’s reaction
(b) Coupling reaction (Comptt. All India 2012)
(a) Aniline and Ethylamine
(b) Ethylamine and Dimethylamine (Comptt. Delhi 2013)
(i) Hoffmann-bromamide degradation reaction
(ii) Carbylamine reaction
(ii) Benzyl chloride to 2-phenylethanamine
(iii) Aniline to benzyl alcohol. (Delhi 2012)
(b) Arrange the following in the increasing order of their basic character in an aqueous solution :
C2H5NH2, (C2H5)2NH, (C3H5)3N
(c) Give a simple chemical test to distinguish between the following pair of compounds :
C6H5—NH2 and C6H5—NH—CH3 (All India 2015)
(ii) a glycosidic linkage.
(i) Invert sugar
(ii) Polypeptides (Delhi 2009)
(i) Hydroxylamine
(ii) Acetic anhydride. (Comptt. All India 2012)
(i) Peptide linkage
(ii) Primary structure
(iii) Denaturation (All India 2012)
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