D-Block Elements Overview and Exercises
D-Block Elements Overview and Exercises
EXERCISE-I
Select one or more than one correct options.
Q.1 (T) imparts violet colour in the flame test
NH3 soln.
(W)Red ppt. ⟶ (X)
dil HCl
(W)Red ppt. ⟶ (Y)white ppt.
NaOH
Δ
(U) ⟶ (Z)gas (gives white fumes with HCl )
sublimes on heating
Identify (𝐓) to (𝐙).
(A) T = KMnO4 , U = HCl, V = Cl2 , W = HgI2 , X = Hg(NH2 )NO3 , Y = Hg 2 Cl2 , Z = N2
(B) T = K 2 Cr2 O7 , U = NH4 Cl, V = CrO2 Cl2 , W = Ag 2 CrO4 , X = [Ag(NH3 )2 ]+ , Y = AgCl, Z = NH3
(C) T = K 2 CrO4 , U = KCl, V = CrO2 Cl2 , W = HgI2 , X = Na2 CrO4 , Y = BaCO3 , Z = NH4 Cl
(D) T = K 2 MnO4 , U = NaCl, V = CrO3 , W = AgNO2 , X = (NH4 )2 CrO4 , Y = CaCO3 , Z = SO2
Q.2 The number of moles of acidified KMnO4 required to convert one mole of sulphite ion into
sulphate ion is
(A) 2/5 (B) 3/5 (C) 4/5 (D) 1
Fe+Mo
Q.3 N2 ( g) + 3H2 ( g) ⇌ 2NH3 ( g); Haber's process, Mo is used as
(A) a catalyst (B) a catalytic promoter
(C) an oxidising agent (D) as a catalytic poison
Q.4 Potash alum is a double salt, its aqueous solution shows the characteristics of
(A) Al3+ ions (B) K + ions (C) SO4 2− ions (D) Al3+ ions but not K + ions
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Q.14 A compound of mercury used in cosmetics, in Ayurvedic and Yunani medicines and known as
Vermilon is
(A) HgCl2 (B) HgS (C) Hg 2 Cl2 (D) HgI
KI dil 2 SO4
Q.15 ↑ Y(g) ⟵ CuSO4 ⟶ X (Blue colour), X and Y are
(A) X = I2 , Y = [Cu(H2 O)4 ]2+ (B) X = [Cu(H2 O)4 ]2+ , Y = I2
(C) X = [Cu(H2 O)4 ]+ , Y = I2 (D) X = [Cu(H2 O)5 ]2+ , Y = I2
Q.16 (NH4 )2 Cr2 O7 (Ammonium dichromate) is used in fireworks. The green coloured powder blown
in air is
(A) Cr2 O3 (B) CrO2 (C) Cr2 O4 (D) CrO3
Q.17 The d-block element which is a liquid at room temperature, having high specific heat, less
reactivity than hydrogen and its chloride (MX 2 ) is volatile on heating is
(A) Cu (B) Hg (C) Ce (D) Pm
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Q.25
Q.26 When KMnO4 solution is added to hot oxalic acid solution, the decolourisation is slow in the
beginning but becomes instantaneous after some time. This is because
(A) Mn2+ acts as auto catalyst (B) CO2 is formed
(C) Reaction is exothermic (D) MnO− 4 catalyses the reaction.
Q.27 The higher oxidation states of transition elements are found to be in the combination with A
and B, which are
(A) F, O (B) O, N (C) O, Cl (D) F, Cl
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Q.28 An element of 3d-transition series shows two oxidation states x and y, differ by two units then
(A) compounds in oxidation state x are ionic if x > y
(B) compounds in oxidation state x are ionic if x < y
(C) compounds in oxidation state y are covalent if x < y
(D) compounds in oxidation state y are covalent if y < x
Q.30 1 mole of Fe2+ ions are oxidised to Fe3+ ions with the help of (in acidic medium)
(A) 1/5 moles of KMnO4 (B) 5/3 moles of KMnO4
(C) 2/5 moles of KMnO4 (D) 5/2 moles of KMnO4
Q.32 To an acidified dichromate solution, a pinch of Na2 O2 is added and shaken. What is observed:
(A) blue colour (B) Orange colour changing to green
(C) Copious evolution of oxygen (D) Bluish - green precipitate
Q.33 The rusting of iron is formulated as Fe2 O3 ⋅ xH2 O which involves the formation of
(A) Fe2 O3 (B) Fe(OH)3 (C) Fe(OH)2 (D) Fe2 O3 + Fe(OH)3
Q.36 A metal M which is not affected by strong acids like conc. HNO3 , conc. H2 SO4 and conc. solution
of alkalis like NaOH, KOH forms MCl3 which finds use for toning in photography. The metal M is
(A) Ag (B) Hg (C) Au (D) Cu
Q.37 Solid CuSO4 ⋅ 5H2 O having covalent, ionic as well as co-ordinate bonds. Copper atom/ion forms
co-ordinate bonds with water.
(A) 1 (B) 2 (C) 3 (D) 4
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Q.42 Number of moles of SnCl2 required for the reduction of 1 mole of K 2 Cr2 O7 into Cr2 O3 is
(in acidic medium)
(A) 3 (B) 2 (C) 1 (D) 1/3
Q.47 In nitroprusside ion, the iron exists as Fe2+ and NO as NO+ rather than Fe3+ and NO
respectively. These forms of ions are established with the help of
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Q.49 Transition elements in lower oxidation states act as Lewis acid because
(A) they form complexes (B) they are oxidising agents
(C) they donate electrons (D) they do not show catalytic properties
Q.51 The Ziegler-Natta catalyst used for polymerisation of ethene and styrene is TiCl4 + (C2 H5 )3 Al,
the catalysing species (active species) involved in the polymerisation is
(A) TiCl4 (B) TiCl3 (C) TiCl2 (D) TiCl
Q.52 Ion(s) having non zero magnetic moment (spin only) is/are
(A) Sc 3+ (B) Ti3+ (C) Cu2+ (D) Zn2+
Q.53 The electrons which take part in order to exhibit variable oxidation states by transition metals
are
(A) ns only (B) (n − 1)d only
(C) ns and (n-1)d only but not np (D) (n-1)d and np only but not ns
Q.56 Colourless solutions of the following four salts are placed separately in four different test tubes
and a strip of copper is dipped in each one of these. Which solution will turn blue?
(A) KNO3 (B) AgNO3 (C) Zn(NO3 )2 (D) ZnSO4
Q.58 When acidified KMnO4 is added to hot oxalic acid solution, the decolourization is slow in the
beginning, but becomes very rapid after some time. This is because:
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Question No. 59 to 68
Questions given below consist of two statements each printed as Assertion (A) and Reason (R);
while answering these questions you are required to choose any one of the following four
responses:
(A) if both (A) and (R) are true and (R) is the correct explanation of (A)
(B) if both (A) and (R) are true but (R) is not correct explanation of (A)
(C) if (A) is true but (R) is false
(D) if (A) is false and (R) is true
Q.59 Assertion: KMnO4 is purple in colour due to charge transfer.
Reason: In MnO− 4 , there is no electron present in d-orbitals of manganese.
Q.62 Assertion: CrO3 reacts with HCl to form chromyl chloride gas.
Reason: Chromyl chloride (CrO2 Cl2 ) has tetrahedral shape.
Q.63 Assertion: Zinc does not show characteristic properties of transition metals.
Reason: In zinc outermost shell is completely filled.
Q.65 Assertion: Equivalent mass of KMnO4 is equal to one-third of its molecular mass when it acts as
an oxidising agent in an alkaline medium.
Reason: Oxidation number of Mn is +7 in KMnO4 .
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EXERCISE-II
JEE-MAIN
1. Number of electrons transferred in each case when KMnO4 acts as an oxidising agent to give
MnO2 , Mn2+ , Mn(OH)3 and MnO4 2− are respectively : [AIEEE 2002, 3/225]
(A) 3,5,4 and 1 (B) 4,3,1 and 5
(C) 1,3,4 and 5 (D) 5,4,3 and 1
2. Which of the following ions has the maximum magnetic moment? [AIEEE 2002, 3/225]
(A) Mn 2+
(B) Fe 2+
(C) Ti 2+
(D) Cr .
2+
4. What would happen when a solution of potassium chromate is treated with an excess of dilute
HNO3 ? [AIEEE 2003, 3/225]
(A) Cr2 O7 and H2 O are formed
2−
(B) CrO4 is reduced to +3 state of Cr
2−
5. Which one of the following nitrates will leaves behind a metal on strong heating ?
[AIEEE 2003, 3/225]
(A) Copper nitrate (B) Manganese nitrate
(C) Silver nitrate (D) Ferric nitrate
6. The atomic numbers of V, Cr, Mn and Fe are respectively 23,24,25 and 26 . Which one of these
may be expected to have the highest second ionization enthalpy? [AIEEE 2003, 3/225]
(A) Cr (B) Mn (C) Fe (D) V
8. The number of d-electrons retained in Fe2+ (At. no. Fe = 26 ) ions are: [AIEEE 2003, 3/225]
(A) 3 (B) 4 (C) 5 (D) 6
9. Ammonia forms the complex ion [Cu(NH3 )4 ]2+ with copper ions in the alkaline solutions but
not in acidic solutions. What is the Statement-2 for it? [AIEEE 2003, 3/225]
(A) In acidic solutions hydration protects copper ions
(B) In acidic solutions protons co-ordinate with ammonia molecules forming NH4 + ions and
NH3 molecules are not available.
(C) In alkaline solutions insoluble Cu(OH)2 is precipitated which is soluble in excess of any
alkali
(D) Copper hydroxide is an amphoteric substance.
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10. The radius of La3+ (Atomic number of La = 57 ) is 1.06Å. Which one of the following given
values will be closest to the radius of Lu3+ (Atomic number of Lu = 71 )?
[AIEEE 2003, 3/225]
(A) 1.60Å (B) 1.40Å (C) 1.06Å (D) 0.85Å
11. Cerium (Z = 58) is an important member of the lanthanoide. Which of the following statement
about cerium is incorrect? [AIEEE 2004, 3/225]
(A) The common oxidation state of cerium are +3 and +4 .
(B) The +3 oxidation state of cerium is more stable than +4 oxidation state.
(C) The +4 oxidation state of cerium is not known in solution.
(D) Cerium (IV) acts as an oxidizing agent.
12. The lanthanide contraction is responsible for the fact that [AIEEE 2005, 3/225]
(A) Zr and Y have about the same radius
(B) Zr and Nb have similar oxidation state
(C) Zr and Hf have about the same radius
(D) Zr and Zn have same oxidation state.
13. Which of the following factors may be regarded as the main cause of lanthanide contraction ?
[AIEEE 2005, 41/2/225]
(A) Greater shielding of 5 d electrons by 4f electrons
(B) Poorer shielding of 5 d electron by 4f electrons
(C) Effective shielding of one of 4f electrons by another in the sub-shell
(D) Poor shielding of one of 4f electron by another in the sub-shell.
14. The "spin-only"' magnetic moment [in units of Bohr magneton, (μB ) of Ni2+ in aqueous solution
would be (atomic number of Ni = 28 ) [AIEEE 2006, 3/165]
(A) 2.84 (B) 4.90 (C) 0 (D) 1.73
16. Identify the incorrect statement among the following. [AIEEE 2007, 3/120]
(A) The chemistry of various lanthanoids is very similar.
(B) 4f and 5 forbitals are equally shielded.
(C) d-block elements show irregular and erratic chemical properties among themselves.
(D) La and Lu have partially filled d orbitals and no other partially filled orbitals.
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17. The actinoids exhibit more number of oxidation states in general than the lanthanoids. This is
because [AIEEE 2007, 3/120]
(A) The actinoids are more reactive than the lanthanoids.
(B) The 5 forbitals extend farther from the nucleus than the 4 orbitals.
(C) The 5 f orbitals are more buried than the 4 forbitals
(D) There is a similarity between 4f and 5f orbitals in their angular part of the wave function
18. Larger number of oxidation states are exhibited by the actinoids than those by the lanthanoids,
the main reason being. [AIEEE 2008, 3/105]
(A) lesser energy difference between 5f and 6 d than between 4f and 5 d orbitals
(B) more energy difference between 5f and 6 d than between 4f and 5 d orbitals
(C) more reactive nature of the actinoids than the lanthanoids
(D) 4f orbitals more diffused than the 5 forbitals
19. In context with the transition elements, which of the following statements is incorrect?
[AIEEE 2009, 4/144]
(A) In the highest oxidation states, the transition metal show basic character and form cationic
complexes.
(B) In the highest oxidation states of the first five transition elements ( Sc to Mn), all the 4 s and
3 d electrons are used for bonding.
(C) Once the d5 configuration is exceeded, the tendency to involve all the 3 d electrons in
bonding decreases.
(D) In addition to the normal oxidation states, the zero oxidation state is also shown by these
elements in complexes.
20. Knowing that the Chemistry of lanthanoids (Ln) is dominated by its +3 oxidation state, which
of the following statement is incorrect? [AIEEE 2009, 4/144]
(A) The ionic sizes of Ln (III) decrease in general with increasing atomic number.
(B) Ln (III) compounds are generally colourless.
(C) Ln (III) hydroxides are mainly basic in character
(D) Because of the large size of the Ln (III) ions the bonding in its compounds is predominently
ionic in character.
0
21. The correct order of EM 2+ /M values with negative sign for the four successive elements Cr, Mn,
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22. In context of the lanthanoids, which of the following statement is not correct?
[AIEEE 2011, 4/120]
(A) There is a gradual decrease in the radii of the members with increasing atomic number in
the series.
(B) All the member exhibit +3 oxidation state.
(C) Because of similar properties the separation of lanthanoids is not easy.
(D) Availability of 4f electrons results in the formation of compounds in +4 state for all the
members of the series.
23. The outer electron configuration of Lu (Atomic No : 71) is : [AIEEE 2011, 4/120]
(A) 4f 3 5 d5 6 s 2 (B) 4f 8 5 d0 6 s 2 (C) 4f 4 5d4 6s2 (D) 4f 14 5 d1 6 s2
24. Iron exhibits +2 and +3 oxidation states. Which of the following statements about iron is
incorrect ? [AIEEE 2012, 4/120]
(A) Ferrous oxide is more basic in nature than the ferric oxide.
(B) Ferrous compounds are relatively more ionic than the corresponding ferric compounds
(C) Ferrous compounds are less volatile than the corresponding ferric compounds
(D) Ferrous compounds are more easily hydrolysed than the corresponding ferric compounds.
25. Which of the following arrangements does not represent the correct order of the property
stated against it? [JEE(Main) 2013, 4/120]
(A) V < Cr < Mn < Fe : paramagnetic behaviour
2+ 2+ 2+ 2+
(B) Ni2+ < Co2+ < Fe2+ < Mn2+ : ionic size
(C) Co3+ < Fe3+ < Cr 3+ < Sc 3+ : stability in aqueous solution
(D) Sc < Ti < Cr < Mn : number of oxidation states
26. Four successive members of the first row transition elements are listed below with atomic
0
numbers. Which one of them is expected to have the highest EM 3+ /M2+ value ?
27. Which series of reactions correctly represents chemical relations related to iron and its
compound? [JEE(Main) 2014, 4/120]
dill H2 SO4 H2 SO4 ,O2 heat
(A) Fe ⟶ FeSO4 ⟶ Fe2 (SO4 )3 ⟶ Fe
O2 , heat dill 2 SO4 heat
(B) Fe ⟶ FeO ⟶ FeSO4 ⟶ Fe
Cl2 , heat heat,air Zn
(C) Fe ⟶ FeCl3 ⟶ FeCl2 ⟶ Fe
O2 ,heat CO,600∘ C CO,700∘ C
(D) Fe ⟶ Fe3 O4 ⟶ FeO ⟶ Fe
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28. The equation which is balanced and represents the correct product(s) is :
[JEE(Main) 2014, 4/120]
(A) Li2 O + 2KCl → 2LiCl + K 2 O
(B) [CoCl(NH3 )5 ]+ + 5H + → Co2+ + 5NH4+ + Cl−
excess, NaOH
(C) [Mg(H2 O)6 ]2+ + ( EDTA )4− ⟶ [Mg( EDTA )]2+ + 6H2 O
(D) CuSO4 + 4KCN → K 2 [Cu(CN)4 ] + K 2 SO4
30. When XO2 is fused with an alkali metal hydroxide in presence of an oxidizing agent such as
KNO3 ; a dark green product is formed which disproportionates in acidic solution to afford a
dark purple solution. X is : [JEE(Main) 2018(online)]
(A) Ti (B) V (C) Cr (D) Mn
31. The transition element that has lowest enthalpy of atomisation is : [JEE-Main 2019]
(A) Zn (B) Cu (C) Fe (D) V
33. The electrolytes usually used in the electroplating of gold and silver, respectively, are :
[JEE-Main 2019]
(A) [Au(CN2 )] and [Ag(CN)2 ]
− −
(B) [Au(NH3 )2] and [Ag(CN)2 ]−
+
34. The element that usually does NOT show variable oxidation states is : [JEE-Main 2019]
(A) Cu (B) Sc (C) V (D) Ti
35. The correct order of the first ionization enthalpies is: [JEE-Main 2019]
(A) Ti < Mn < Zn < Ni (B) Ti < Mn < Ni < Zn
(C) Mn < Ti < Zn < Ni (D) Zn < Ni < Mn < Ti
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36. Thermal decomposition of a Mn compound (X) at 513K results in compound Y, MnO2 and a
gaseous product MnO2 reacts with NaCl and concentrated H2 SO4 to give pungent gas Z. X, Y, and
Z, respectively, are: [Main April 12, 2019]
(A) KMnO4 , K 2 MnO4 and Cl2 (B) K 2 MnO4 , KMnO4 and SO2
(C) K 3 MnO4 , K 2 MnO4 and Cl2 (D) K 2 MnO4 , KMnO4 and Cl2
37. Match the catalysts (Column-I) with products (Column-II) [Main April 9, 2019]
Column-1 Column-2
(Catalyst) (Product)
(A) V2 O5 (i) Polyethylene
(B) TiCl4 /Al(Me)3 (ii) ethanol
(C) PdCl2 (iii) H2SO4
(D) Iron Oxide (iv) NH3
(A) (A)-(iii); (B)-(iv); (C)-(i); (D)-(ii)
(B) (A)-(ii);(B)-(iii); (C)-(i); (D)-(iv)
(C) (A)-(iii); (B)-(i); (C)-(ii); (D)-(iv)
(D) (A)-(iv); (B)-(iii); (C)-(ii); (D)-(i)
41. Identify the element for which electronic configuration in +3 oxidation state is [Ar]3d5 :
[Main Sep. 1, 2021]
(A) Ru (B) Mn (C) Co (D) Fe
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43. In the ground state of atomic Fe(Z = 26), the spin-only magnetic moment is _______ × 10−1 BM.
(Round off to the nearest integer).
[Given : √3 = 1.73, √2 = 1.41] [Main March 17, 2021 (III)]
44. The reaction of zinc with excess of aqueous alkali, evolves hydrogen gas and gives
[Main July 29, 2022]
(A) Zn(OH)2 (B) ZnO (C) [Zn(OH)4 ]2− (D) [ZnO2 ]2−
45. The total number of Mn = O bonds in Mn2 O7 is [Main July 27, 2022]
(A) 4 (B) 5 (C) 6 (D) 3
46. Dihydrogen reacts with CuO to give [Main June 28, 2022]
(A) CuH2 (B) Cu (C) Cu2 O (D) Cu(OH)2
47. Among the following, which is the strongest oxidizing agent? [Main June 25, 2022]
(A) Mn3+ (B) Fe3+ (C) Ti3+ (D) Cr 3+
compounds A and B. If the oxidation state of Mn in B is smaller than that of A, then the spin-
only magnetic moment (μ) value of B in BM is ________ . (Nearest integer)
49. The spin-only magnetic moment value of the compound with strongest oxidizing ability among
MnF4 , MnF3 and MnF2 is ________ B.M. [nearest integer] [Main July 26, 2022 (II)]
50. The spin-only magnetic moment value of M 3+ ion (in gaseous state) from the pairs
Cr 3+ /Cr 2+ , Mn3+ /Mn2, Fe3+ /Fe2+ and Co3+ /Co2+ that has negative standard electrode
potential is _________ B.M. [Nearest integer] [Main July 25, 2022 (II)]
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51. The number of statement(s) correct from the following for copper (at no. 29) is/are ________ .
52. Acidified potassium permanganate solution oxidises oxalic acid. The spin-only magnetic
moment of the manganese product formed from the above reaction is ________ . B.M. (Nearest
Integer) [Main June 27, 2022 (I)]
53. The transition metal having highest 3rd ionisation enthalpy is : [JEE MAIN 2024]
(A) Cr (B) Mn (C) V (D) Fe
54. Given below are two statements : one is labelled as Assertion (A) and the other is labelled as
Reason (R). [JEE MAIN 2024]
Assertion (A) : In aqueous solutions Cr 2+ is reducing while Mn3+ is oxidising in nature.
Reason (R) : Extra stability to half filled electronic configuration is observed than incompletely
filled electronic configuration.
In the light of the above statement, choose the most appropriate answer from the options given
below:
(A) Both (A) and (R) are true and (R) is the correct explanation of (A)
(B) Both (A) and (R) are true but (R) is not the correct explanation of (A)
(C) (A) is false but (R) is true
(D) (A) is true but (R) is false
55. Which of the following compounds show colour due to d-d transition? [JEE MAIN 2024]
(A) CuSO4 . 5H2 O (B) K 2 Cr2 O7
(C) K 2 CrO4 (D) KMnO4
56. NaCl reacts with conc. H2 SO4 and K 2 Cr2 O7 to give reddish fumes (B), which react with NaOH to
give yellow solution (C). (B) and (C) respectively are ; [JEE MAIN 2024]
(A) CrO2 Cl2 , Na2 CrO4 (B) Na2 CrO4 , CrO2 Cl2
(C) CrO2 Cl2 , KHSO4 (D) CrO2 Cl2 , Na2 Cr2 O7
57. Choose the correct option having all the elements with d10 electronic configuration from the
following: [JEE MAIN 2024]
(A) 27
Co, 28
Ni, 26
Fe, 24
Cr (B) 29
Cu, 30
Zn, 48
Cd, 47
Ag
(C) 46
Pd, 28
Ni, 26
Fe, 24
Cr (D) 28
Ni, 24
Cr, 26
Fe, 29
Cu
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58. In chromyl chloride test for confirmation of Cl− ion, a yellow solution is obtained. Acidification
of the solution and addition of amyl alcohol and 10% H2 O2 turns organic layer blue indicating
formation of chromium pentoxide. The oxidation state of chromium in that is
[JEE MAIN 2024]
(A) +6 (B) +5 (C) +10 (D) +3
60. Which of the following statements are correct about Zn, Cd and Hg ? [JEE MAIN 2024]
A. They exhibit high enthalpy of atomization as the d-subshell is full.
B. Zn and Cd do not show variable oxidation state while Hg shows +I and + II.
C. Compounds of Zn, Cd and Hg are paramagnetic in nature.
D. Zn, Cd and Hg are called soft metals.
Choose the most appropriate from the options given below:
(A) B, D only (B) B, C only
(C) A, D only (D) C, D only
62. The orange colour of K 2 Cr2 O7 and purple colour of KMnO4 is due to [JEE MAIN 2024]
(A) Charge transfer transition in both.
(B) d → d transition in KMnO4 and charge transfer transitions in K 2 Cr2 O7 .
(C) d → d transition in K 2 Cr2 O7 and charge transfer transitions in KMnO4 .
(D) d → d transition in both.
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63. Alkaline oxidative fusion of MnO2 gives "A" which on electrolytic oxidation in alkaline solution
produces B. A and B respectively are: [JEE MAIN 2024]
(A) Mn2 O7 and MnO−
4 (B) MnO4 2− and MnO−
4
64. A and B formed in the following reactions are: [JEE MAIN 2024]
CrO2 Cl2 + 4NaOH → A + 2NaCl + 2H2 O
A + 2HCl + 2H2 O2 → B + 3H2 O
(A) A = Na2 CrO4 , B = CrO5 (B) A = Na2 Cr2 O4 , B = CrO4
(C) A = Na2 Cr2 O7 , B = CrO3 (D) A = Na2 Cr2 O7 , B = CrO5
66. Choose the correct statements from the following [JEE MAIN 2024]
A. Mn2 O7 is an oil at room temperature
B. V2 O4 reacts with acid to give VO2+
2
67. The 'Spin only' Magnetic moment for [Ni(NH3 )6 ]2+ is ____ × 10−1 BM. [JEE MAIN 2024]
(given = Atomic number of Ni: 28)
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69. In the reaction of potassium dichromate, potassium chloride and sulfuric acid (conc.), the
oxidation state of the chromium in the product is (+) ______. [JEE MAIN 2024]
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EXERCISE-III
JEE-ADVANCED
1. Amongst the following identify the species with an atom in +6 oxidation state.
[JEE 2000, 3/35]
(A) MnO4
−
(B) Cr(CN)6 3−
(C) NiF6
2−
(D) CrO2 Cl2
5. When MnO2 is fused with KOH, a coloured compound is formed. The product and its colour is:
[JEE 2003, 3/144]
(A) K 2 MnO4 , green (B) Mn2 O3 , brown
(C) Mn2 O4 , black (D) KMnO4 , purple
7. The pair of compounds having metals in their highest oxidation state is:[JEE 2004, 3/144]
(A) MnO2 , FeCl3 (B) [MnO4 ]− , CrO2 Cl2
(C) [Fe(CN)6]2− , [Co(CN)6 ]3− (D) [NiCl4 ]2− , [Ni(CO)4 ].
8. Which of the following pair of compounds is expected to exhibit same colour in aqueous
solution? [JEE 2005, 3/84]
(A) FeCl3 , CuCl2 (B) VOCl2 , CuCl2 (C) VOCl2 , FeCl2 (D) FeCl2 , MnCl2
9. Give equations and describe the process for the developing of black and white photographic
film. When sodium thiosulphate solution is treated with acidic solution turns milky white. Give
the half reaction of the above described process. [JEE 2005, 4/60]
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Identify (A), (B) and (C). Also explain colour difference between MCl4 and (B).
11. Match the reactions in Column I with nature of the reactions/type of the products in Column II.
[JEE 2007, 6/162]
Column I Column II
(A) O2 → O2 + O2
− 2−
(P) Redox reaction
(B) CrO4 + H →
2− +
(Q) One of the products has trigonal planar structure
(C) MnO4 + NO2 + H →
− − +
(R) Dimeric bridged tetrahedral metal ion
(D) NO3 + H2 SO4 + Fe →
− 2+
(S) Disproportionation
12. Among the following, the coloured compound is : [JEE 2008, 3/163]
(A) CuCl (B) K 3 [Cu(CN)4 ] (C) CuF2 (D) [Cu(CH3 CN)4 ]BF4
13. The oxidation number of Mn in the product of alkaline oxidative fusion of MnO2 is.
[JEE 2009, 4/160]
14. Reduction of the metal centre in aqueous permanganate ion involves: [JEE 2011, 4/180]
(A) 3 electrons in neutral medium (B) 5 electrons in neutral medium
(C) 3 electrons in alkaline medium (D) 5 electrons in acidic medium
15. The colour of light absorbed by an aqueous solution of CuSO4 is: [JEE 2012, 3/136]
(A) organge-red (B) blue-green (C) yellow (D) violet
16. Which of the following halides react(s) with AgNO3 (aq) to give a precipitate that dissolves in
Na2 S2 O3 (aq) ? [JEE 2012, 4/136]
(A) HCl (B) HF (C) HBr (D) HI
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18. The correct statement(s) about Cr 2+ and Mn3+ is (are) : [JEE(Advanced) 2015, 4/168]
[Atomic numbers of Cr = 24 and Mn = 25 ]
(A) Cr 2+ is a reducing agent
(B) Mn3+ is an oxidizing agent
(C) Both Cr 2+ and Mn3+ exhibit d4 electronic configuration
(D) When Cr 2+ is used as a reducing agent, the chromium ion attains d5 electronic
configuration.
20. Fusion of MnO2 with KOH in presence of O2 produces a salt W. Alkaline solution of W upon
electrolytic oxidation yields another salt X. The manganese containing ion's present in W and X,
respectively, are Y and Z. Correct statement(s) is(are) [JEE(Advanced) 2019]
(1) Y is diamagnetic in nature while Z is paramagnetic
(2) In aqueous acidic solution, Y undergoes disproportionation reaction to give Z and MnO2
(3) Both Y and Z are coloured and have tetrahedral shape
(4) In both Y and Z, π-bonding occurs between p-orbitals of oxygen and d-orbitals of
manganese
21. An acidified solution of potassium chromate was layered with an equal volume of amyl alcohol.
When it was shaken after the addition of 1 mL of 3%H2 O2 , a blue alcohol layer was obtained.
The blue color is due to the formation of a chromium (VI) compound ' X '. What is the number
of oxygen atoms bonded to chromium through only single bonds in a molecule of X ?
[JEE(Advanced) 2020]
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NCERT EXAMPLER
Multiple Choice Questions (Type-I)
1. Electronic configuration of a transition element X in +3 oxidation state is [Ar]3 d5 . What is its
atomic number?
(A) 25 (B) 26 (C) 27 (D) 24
2. The electronic configuration of Cu(II) is 3 d9 whereas that of Cu(I) is 3 d10 . Which of the
following is correct?
(A) Cu (II) is more stable
(B) Cu(II) is less stable
(C) Cu(I) and Cu (II) are equally stable
(D) Stability of Cu(I) and Cu(II) depends on nature of copper salts
3. Metallic radii of some transition elements are given below. Which of these elements will have
highest density?
Element Fe Co Ni Cu
Metallic radii/pm 126 125 125 128
(A) Fe (B) Ni (C) Co (D) Cu
4. Generally transition elements form coloured salts due to the presence of unpaired electrons.
Which of the following compounds will be coloured in solid state?
(A) Ag 2 SO4 (B) CuF2 (C) ZnF2 (D) Cu2 Cl2
6. The magnetic nature of elements depends on the presence of unpaired electrons. Identify the
configuration of transition element, which shows highest magnetic moment.
(A) 3d7 (B) 3d5 (C) 3 d8 (D) 3d2
8. When KMnO4 solution is added to oxalic acid solution, the decolourisation is slow in the
beginning but becomes instantaneous after some time because
(A) CO2 is formed as the product. (B) Reaction is exothermic.
(C) MnO4 catalyses the reaction.
−
(D) Mn2+ acts as autocatalyst.
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9. KMnO4 acts as an oxidising agent in acidic medium. The number of moles of KMnO4 that will be
needed to react with one mole of sulphide ions in acidic solution is
2 3 4 1
(A) 5 (B) 5 (C) 5 (D) 5
11. Interstitial compounds are formed when small atoms are trapped inside the crystal lattice of
metals. Which of the following is not the characteristic property of interstitial compounds?
(A) They have high melting points in comparison to pure metals.
(B) They are very hard.
(C) They retain metallic conductivity.
(D) They are chemically very reactive.
12. The magnetic moment is associated with its spin angular momentum and orbital angular
momentum. Spin only magnetic moment value of Cr 3+ ion is__________.
(A) 2.87 B.M. (B) 3.87 B.M. (C) 3.47 B.M. (D) 3.57 B.M.
13. KMnO4 acts as an oxidising agent in alkaline medium. When alkaline KMnO4 is treated with KI,
iodide ion is oxidised to__________.
(A) I2 (B) IO− (C) IO−
3 (D) IO−4
15. When acidified K 2 Cr2 O7 solution is added to Sn2+ salts then Sn2+ changes to
(A) Sn (B) Sn3+ (C) Sn4+ (D) Sn+
16. Highest oxidation state of manganese in fluoride is +4(MnF4 ) but highest oxidation state in
oxides is +7(Mn2 O7 ) because
(A) fluorine is more electronegative than oxygen.
(B) fluorine does not possess d-orbitals.
(C) fluorine stabilises lower oxidation state.
(D) in covalent compounds fluorine can form single bond only while oxygen forms double
bond.
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17. Why is HCl not used to make the medium acidic in oxidation reactions of KMnO4 in acidic
medium?
(A) Both HCl and KMnO4 act as oxidising agents.
(B) KMnO4 oxidises HCl into Cl2 which is also an oxidising agent.
(C) KMnO4 is a weaker oxidising agent than HCl.
(D) KMnO4 acts as a reducing agent in the presence of HCl.
18. Transition elements show magnetic moment due to spin and orbital motion of electrons. Which
of the following metallic ions have almost same spin only magnetic moment?
(A) Co2+ (B) Cr 2+ (C) Mn2+ (D) Cr 3+
19. In the form of dichromate, Cr(VI) is a strong oxidising agent in acidic medium but Mo(VI) in
MoO3 and W(VI) in WO3 are not because
(A) Cr(VI) is more stable than Mo(VI) and W(VI).
(B) Mo(VI) and W(VI) are more stable than Cr(VI).
(C) Higher oxidation states of heavier members of group-6 of transition series are more stable.
(D) Lower oxidation states of heavier members of group-6 of transition series are more stable.
20. Which of the following ions show higher spin only magnetic moment value?
(A) Ti3+ (B) Mn2+ (C) Fe3+ (D) Co3+
21. Transition elements form binary compounds with halogens. Which of the following elements
will form MF3 type compounds?
(A) Cr (B) Co (C) Cu (D) Ni
24. Why E 0 values for Mn, Ni and Zn are more negative than expected?
27. When Cu2+ ion is treated with KI, a white precipitate is formed. Explain the reaction with the
help of chemical equation.
28. Out of Cu2 Cl2 and CuCl2 , which is more stable and why?
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29. When a brown compound of manganese (A) is treated with HCl it gives a gas (B). The gas taken
in excess, reacts with NH3 to give an explosive compound (C). Identify compounds A, B and C.
30. Although fluorine is more electronegative than oxygen, but the ability of oxygen to stabilise
higher oxidation states exceeds that of fluorine. Why?
31. Although Cr 3+ and Co2+ ions have same number of unpaired electrons but the magnetic
moment of Cr 3+ is 3.87 B.M. and that of Co2+ is 4.87 B.M. Why?
32. Explain why does colour of KMnO4 disappear when oxalic acid is added to its solution in acidic
medium.
34. A solution of KMnO4 on reduction yields either a colourless solution or a brown precipitate or a
green solution depending on pH of the solution. What different stages of the reduction do these
represent and how are they carried out?
36. The halides of transition elements become more covalent with increasing oxidation state of the
metal. Why?
37. While filling up of electrons in the atomic orbitals, the 4 s orbital is filled before the 3 d orbital
but reverse happens during the ionisation of the atom. Explain why?
38. Reactivity of transition elements decreases almost regularly from Sc to Cu. Explain.
39. Match the catalysts given in Column I with the processes given in Column II.
Column I (Catalyst) Column II (Process)
(A) Ni in the presence of hydrogen (i) Zieglar Natta catalyst
(B) Cu2 Cl2 (ii) Contact process
(C) V2 O5 (iii) Vegetable oil to ghee
(D) Finely divided iron (iv) Sandmeyer reaction
(E) TiCl4 + Al(CH3 )3 (v) Haber's Process
(F) Decomposition of KClO3
40. Match the properties given in Column I with the metals given in Column II.
Column I (Property) Column II (Metal)
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41. Match the solutions given in Column I and the colours given in Column II.
Column I (Aqueous solution of salt) Column II (Colour)
(A) FeSO4 ⋅ 7H2 O (i) Green
(B) NiCl2 ⋅ 4H2 O (ii) Light pink
(C) MnCl2 ⋅ 4H2 O (iii) Blue
(D) CoCl2 ⋅ 6H2 O (iv) Pale green
(E) Cu2 Cl2 (v) Pink
(vi) Colourless
42. Match the properties given in Column I with the metals given in Column II.
Column I (Property) Column II (Metal)
(A) Element with highest second ionisation enthalpy (i) Co
(B) Element with highest third ionisation enthalpy (ii) Cr
(C) M in M(CO)6 is (iii) Cu
(D) Element with highest heat of atomization (iv) Zn
(v) Ni
V. Assertion and Reason Type
Note: In the following questions a statement of assertion followed by a statement of reason is
given. Choose the correct answer out of the following choices.
(A) Both assertion and reason are true, and reason is the correct explanation of the assertion.
(B) Both assertion and reason are true but reason is not the correct explanation of assertion.
(C) Assertion is not true but reason is true.
(D) Both assertion and reason are false.
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47. When a chromite ore (A) is fused with sodium carbonate in free excess of air and the product is
dissolved in water, a yellow solution of compound (B) is obtained. After treatment of this
yellow solution with sulphuric acid, compound (C) can be crystallised from the solution. When
compound (C) is treated with KCl, orange crystals of compound (D) crystallise out. Identify A to
D and also explain the reactions.
48. When an oxide of manganese (A) is fused with KOH in the presence of an oxidising agent and
dissolved in water, it gives a dark green solution of compound (B). Compound (B)
disproportionates in neutral or acidic solution to give purple compound (C). An alkaline
solution of compound (C) oxidises potassium iodide solution to a compound (D) and
compound (A) is also formed. Identify compounds A to D and also explain the reactions
involved.
50. Mention the type of compounds formed when small atoms like H, C and N get trapped inside
the crystal lattice of transition metals. Also give physical and chemical characteristics of these
compounds.
51. (a) Transition metals can act as catalysts because these can change their oxidation state. How
does Fe(III) catalyse the reaction between iodide and persulphate ions?
(b) Mention any three processes where transition metals act as catalysts.
52. A violet compound of manganese (A) decomposes on heating to liberate oxygen and
compounds (B) and (C) of manganese are formed. Compound (C) reacts with KOH in the
presence of potassium nitrate to give compound (B). On heating compound (C) with conc.
H2 SO4 and NaCl, chlorine gas is liberated and a compound (D) of manganese along with other
products is formed. Identify compounds A to D and also explain the reactions involved.
ANSWER KEY
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Do yourself – 1
Question 1 2 3 4 5
Answer B,C,D A,B A A,B B
Do yourself – 2
Question 1 2 3 4 5
Answer A A B D A,B
EXERCISE-I
Q.1 B Q.2 A Q.3 B Q.4 A,B,C Q.5 A,B Q.6 B Q.7 A,B,C,D
Q.8 A Q.9 B Q.10 A Q.11 A,B, D Q.12 A,B,C Q.13 B,C Q.14 B
Q.15 B Q.16 A Q.17 B Q.18 D Q.19 B Q.20 C Q.21 A,B,C
Q.22 A,B,C Q.23 A Q.24 A,B,C Q.25 B Q.26 A Q.27 A Q.28 B,C
Q.29 D Q.30 A Q.31 B Q.32 A,C Q.33 D Q.34 A Q.35 A,B
Q.36 C Q.37 D Q.38 A,B,C,D
Q.39 C Q.40 B Q.41 C Q.42 A Q.43 A,B Q.44 C Q.45 D
Q.46 A Q.47 A Q.48 A,B,C Q.49 A Q.50 A,B Q.51 B Q.52 B,C
Q.53 C Q.54 B Q.55 A Q.56 B Q.57 D Q.58 A Q.59 B
Q.60 B Q.61 A Q.62 B Q.63 C Q.64 C Q.65 B Q.66 A
Q.67 A Q.68 C
EXERCISE-II (JEE-Main)
1. (A) 2. (A) 3. (A) 4. (A) 5. (C) 6. (A) 7. (A)
8. (D) 9. (B) 10. (D) 11. (C) 12. (C) 13. (D) 14. (A)
15. (D) 16. (B) 17. (B) 18. (A) 19. (A) 20. (B) 21. (A)
22. (D) 23. (D) 24. (D) 25. (A) 26. (D) 27. (D) 28. (B)
29. (C) 30. (D) 31. (A) 32. (C) 33. (A) 34. (B) 35. (B)
36. (A) 37. (C) 38. (C) 39. (B) 40. (A) 41. (D) 42. (D)
43. (49) 44. (C) 45. (C) 46. (B) 47. (A) 48. (4) 49. (5)
50. (4) 51. (3) 52. (6) 53. (B) 54. (A) 55. (A) 56. (A)
57. (B) 58. (A) 59. (D) 60. (A) 61. (B) 62. (A) 63. (B)
64. (A) 65. (D) 66. (B) 67. (28) 68. (8) 69. (6)
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JEE-MAIN
SOLUTION
513 K
36. (a) 2KMnO4 ⟶ K 2 MnO4 + MnO2 + O2
(X) (Y) gas
MnO2 + 4NaCl + 4H2 SO4 → MnCl2 + 4NaHSO4 + Cl2 + 2H2 O
Conc. (Z)
Pungent gas
37. (c)
(A) V2 O5 → Preparation of H2 SO4 in contact process
(B) TiCl4 + Al(Me)3 → Polyethylene (Ziegler-Natta catalyst)
(C) PdCl2 → Ethanol (Wacker's process)
(D) Iron oxide → NH3 in (Haber's process)
38. (C)
39. (b) 20 Fe = [Ar]3d6 4s2 . Third ionisation results into stable d5 configuration.
40. (a) Atomic size of elements of 4d and 5d transition series are nearly same due to lanthanide
contraction.
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42. (d) Potassium permanganate on heating at 513 K gives potassium manganate (K 2 MnO4 ) and its
colour is green.
2KMnO4 ⎯⎯⎯
513 K
→ K2MnO4 + MnO2 + O2
Green Black
In K 2 MnO4 , manganese oxidation state is +6 and hence, it as one unpaired electron and
paramagnetic.
47. (a) Strongest oxidising agent have highest reduction potential value.
∘
EMn 3+ /Mn2+ = 1.51 V (highest)
H+
48. MnO2− −
4 ⟶ MnO2 + MnO2
No. of unpaired e− (n) = 3
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(Strongest O.A)
For n = 4,
∴ μ5 = √4(4 + 2) = √24 = 4.89 = 5
50. In case of conversion of Cr 3+ → Cr 2+ the e− is added to eg orbital, hence electrode potential is
negative.
∘
ECr+3 /Cr+2 = −0.41 V
[Cr +3 ] = 4 s0 3 d3
μ = √n(n + 2) B.M = √15 B.M 4 B.M
51. A, B, C are correct and D is incorrect because Fehling solution has Cu (II).
52. 2KMnO4 + 5H2 C2 O4 + 3H2 SO4 →
Mn2+ has 5 unpaired electrons, therefore, the magnetic moment = √5(5 + 2) = √35BM.
53. 3rd Ionisation energy :
V : 2833 KJ/mol
Cr : 2990 KJ/mol
Mn : 3260 KJ/mol
Fe : 2962 KJ/mol
alternative
Mn: 3d5 4s2
Fe: 3d6 4s 2
Cr: 3d5 4s1
V: 3d3 4s 2
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[Link]
CrO24− ⎯⎯⎯⎯⎯
2. Amyl alcohol
3.10%H2O2
→ CrO5
yellow solution blue solution
60. (A) Zn, Cd, Hg exhibit lowest enthalpy of atomization in respective transition series.
(C) Compounds of Zn, Cd and Hg are diamagnetic in nature.
K 2 Cr2 O7 → Cr +6 → No d − d transition
62. 7+ Charge transfer
KMnO4 → Mn → No d − d transition
63. Alkaline oxidative fusion of MnO2 :
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MnO24− → MnO−4 + e−
65. A. CrO2−
4 is tetrahedral
= 28.2 10−1 BM
x = 28
69. K2Cr2O7 (s) + 4KCl(s) + 6H2SO4 (conc.)→ 2CrO2Cl2 (g) + 6KHSO4 + 3H2O
This reaction is called chromyl chloride test.
Here oxidation state of Cr is +6.
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EXERCISE-III (JEE-ADVANCED)
1. (D)
2. C6 H4 (OH)2 + 2AgBr ⟶ 2Ag + C6 H4 O2 + 2HBr.
AgBr + 2Na2 S2 O3 ⟶ Na3 [Ag(S2 O3 )2 ] + NaBr
3. (B) 4. (B) 5. (A) 6. (A) 7. (B) 8. (B)
9. Developer is usually a weak reducing agent like potassium ferrous oxalate, an alkaline solution
of pyrogallol or an alkaline solution of quinol.
In the process of development of the photographic film, the exposed/activated AgBr grains are
preferentially reduced by one of the reducing agent described above.
The photographic film is then fixed by washing with hypo solution to remove the unreduced
AgBr grains from the film.
AgBr + 2Na2 S2 O3 ⟶ Na3 [Ag(S2 O3 )2 ] + NaBr
S2 O3 2− + H2 O ⟶ 2SO2 + 2H + + 4e−
S2 O3 2− + 6H + ⟶ 2 S ↓ ( white milky) + 3H2 O
10. (A) is TiCl4 as it has no unpaired electron and is liquid at room temperature on account of
covalent character because of high polarising power of Ti+4 being covalent gets hydrolysed
forming TiO2 (H2 O)2 and HCl(B) which fumes in air.
In [Ti(H2 O)6 ]Cl3 complex Ti(III) has one unpaired electron (3 d1 ) which gives violet/purple
colour to d-d transition.
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NCERT EXAMPLER
I. Multiple Choice Questions (Type-I)
1. (B) 2. (A) 3. (D) 4. (B) 5. (A) 6. (B) 7. (A)
8. (D) 9. (A) 10. (A) 11. (D) 12. (B) 13. (C) 14. (A)
15. (C) 16. (D) 17. (B)
II. Multiple Choice Questions (Type-II)
18. (A),(D) 19. (B), (C) 20. (B), (C) 21. (A), (B)
22. (B), (C)
III. Short Answer Type
23. Cu shows positive E ⊖ value.
24. Hint : Negative E Θ values for Mn2+ and Zn2+ are related to stabilities of half filled and fully filled
configuration respectively. But for Ni2+ , E Θ value is related to the highest negative enthalpy of
hydration.
25. Ionisation enthalpy of Cr is lower due to stability of d5 and the value for Zn is higher because
its electron comes out from 4 s orbital.
26. The high melting points of transition metals are attributed to the involvement of greater
number of electrons in the interatomic metallic bonding from (n-1) d-orbitals in addition to ns
electrons
27. Hint : Cu2+ gets reduced to Cu+
2Cu2+ + 4Γ → Cu2 I2 + I2
(white precipitate)
28. Hint : CuCl2 is more stable than Cu2 Cl2 . The stability of Cu2+ (aq.) rather than Cu+ (aq.) is due to
the much more negative .hydH Θ of Cu2+ (aq.) than Cu + (aq.).
29. A = MnO2 B = Cl2 C = NCl3
MnO2 + 4HCl → MnCl2 + Cl2 + 2H2 O
(A) (B)
NH3 + 3Cl2 → NCl3 + 3HCl
(excess) (C)
30. Hint: It is due to the ability of oxygen to form multiple bonds to metals.
31. Hint: Due to symmetrical electronic configuration there is no orbital contribution in Cr 3+ ion.
However appreciable orbital contribution takes place in Co2+ ion.
32. KMnO4 acts as oxidising agent. It oxidises oxalic acid to CO2 and itself changes to Mn2+ ion
which is colourless.
5C2 O2− −
4 + 2MnO4 + 16H → 2Mn
+ 2+
+ 8H2 O + 10CO2
(Coloured) (Colourless)
33. Cr2 O72−
Dichromate Chromate
(Orange) (Yellow)
34. Oxidising behaviour of KMnO4 depends on pH of the solution. In acidic medium (pH < 7)
MnO− + −
4 + 8H + 5e → Mn
2+
+ 4H2 O
(Colourless)
In alkaline medium (pH > 7)
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MnO− 4 + e → MnO4
2−
(Green)
In neutral medium (pH = 7)
MnO2− −
4 + 2H2 O + 3e → MnO2 + 4OH
−
(Brown precipitate)
35. Hint: High ionisation enthalpy to transform Cu(s) to Cu2+ (aq) is not balanced by its hydration
enthalpy. However, in case of Zn after removal of electrons from 4 s-orbital, stable 3 d10
configuration is acquired.
36. As the oxidation state increases, size of the ion of transition element decreases. As per Fajan's
rule, as the size of metal ion decreases, covalent character of the bond formed increases.
37. n + l rule : For 3 d = n + l = 54 s = n + l = 4
So electron will enter in 4 s orbital.
Ionisation enthalpy is responsible for the ionisation of atom. 4 s electrons are loosely held by
the nucleus. So electrons are removed from 4 s orbital prior to 3 d.
38. Hint : It is due to regular increase in ionisation enthalpy.
IV. Matching Type
39. (A) → (iii) ; (B) → (iv) ; (C) → (ii) ; (D) → (v) ; (E) → (i)
40. (A) → (iii) ; (B) → (i) ; (C) → (ii)
41. (A) → (iv) ; (B) → (i) ; (C) → (ii) ; (D) → (v) ; (E) → (vi)
42. (A) → (iii) ; (B) → (iv) ; (C) → (ii) ; (D) → (i)
V. Assertion and Reason Type
43. (A) 44. (A) 45. (B)
VI. Long Answer Type
46. A = Cu B = Cu(NO3 )2 C = [Cu(NH3 )4 ] D = CO2
E = CaCO3 F= Cu2 [Fe(CN)6 ] G = Ca(HCO3 )2
CuCO3 → CuO + CO2
CuO + CuS → Cu + SO2
(A)
Cu + 4HNO3 (Conc) → Cu(NO3 )2 + 2NO + 2H2 O
(B)
2+ 3
Cu + NH → [Cu(NH3 )4 ]
(B) (C)
Ca(OH)2 + CO2 → CaCO3 + H2 O
(D) (E)
CaCO3 + H2 O + CO2 → Ca(HCO3 )2
47. A = FeCr2 O4 B = Na2 CrO4 C = Na2 Cr2 O7 ⋅ 2H2 O D = K 2 Cr2 O7
4FeCr2 O4 + 8Na2 CO3 + 7O2 → 8Na2 CrO4 + 2Fe2 O3 + 8CO2
(A) (B)
2NaCrO4 + 2H → Na2 Cr2 O7 + 2Na+ + H2 O
+
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Zinc's low melting point among the 3d transition metals is influenced by its d10 electron configuration, which lacks unpaired electrons necessary for strong metallic bonding. This filled d-subshell acquisition reduces the extent of such metallic bonding compared to metals with partially filled d-subshells, thus resulting in a lower melting point .
Zn, Cd, and Hg do not show variable oxidation states because they have filled d-orbitals (d10 configuration), which are stable. This full d-subshell means they lack d-subshell vacancies required for exhibiting different oxidation states, contrasting with typical transition metals which have partially filled d-orbitals .
Manganese achieves a higher oxidation state of +7 in Mn2O7 (oxides) compared to +4 in MnF4 (fluorides) due to the higher electronegativity and unique bonding capabilities of oxygen. Oxygen's ability to form double bonds and the strength in π-bonding allow for stabilization of higher oxidation states, whereas fluorine’s single-bond formation limits it to lower oxidation states despite its higher electronegativity .
Charge transfer transitions are responsible for the purple color of KMnO4 and the orange color of K2Cr2O7. In KMnO4, the charge transfer occurs from oxygen to manganese, facilitated by high oxidizing capacity, creating highly vibrant chromophores. Similarly, K2Cr2O7's color arises from charge transfer involving Cr-VI, which differs from simple d-d electronic configurational changes .
The solution turns blue upon amyl alcohol and H2O2 addition due to the formation of chromium pentoxide (CrO5), which involves chromium in a +6 oxidation state. This color change signifies the presence of Cl⁻ ions, resulting from the complex formation and subsequent redox activity involving the Cr{VI} species .
In acidic medium, KMnO4 acts as a strong oxidizing agent as it reduces Mn from +7 to +2 while oxidizing other species. It requires 4/5 moles of KMnO4 to fully oxidize one mole of sulfide ions to sulfates, reflecting its potent oxidative capacity which facilitates the electron transfer necessary to complete the redox pair .
Chromate ions (yellow) convert to dichromate ions (orange) as the pH decreases because the equilibrium shifts from CrO4^2− to Cr2O7^2− in acidic conditions. The chromate-dichromate equilibrium is sensitive to pH changes, where adding H+ ions encourages the formation of dichromates, demonstrating Le Châtelier's principle .
Mo acts as a catalytic promoter in the Haber process for ammonia synthesis, enhancing the efficiency of the primary catalyst, typically iron. Unlike catalysts or catalytic poisons, Mo does not change the reaction path but increases the catalyst's lifespan and activity .
In the reaction between KMnO4 and oxalic acid, the decolorization is initially slow, but once Mn2+ ions form, they catalyze the reaction, causing it to proceed rapidly. Mn2+ acts as an autocatalyst by reducing the activation energy, which contrasts the implication of KMnO4 catalysis in facilitating its reduction .
The reducing power increases as the reduction potential becomes more negative. Thus, the order of reducing power is Ca < Mg < Zn < Ni, where Ca, having the most negative reduction potential, acts as the strongest reducing agent. The trend correlates with their ability to lose electrons easily, dictated by the energy required to remove electrons from their valence shells .