Sign in
12thPass logo
New chatPYQ LibraryDoubtsRank report
Sign in to see Recents

Your guest activity stays on this device

Sign in to save progress →
Sign in

Coordination Compounds question

2025 · 29 Jan · Shift 1 · Q4
Guest · filters and generic practice availableBrowsing as a guest · PYQ filters and generic practice are available. Sign in only for personalised features and saved progress.
  1. PYQ Library
  2. /JEE Main
  3. /Chemistry
  4. /Coordination Compounds
  5. /2025 · 29 Jan · Shift 1 · Q4

Coordination Compounds question

2025 · 29 Jan · Shift 1 · Q4

JEE MainChemistryCoordination CompoundsMCQ+4 / −1
The correct increasing order of stability of the complexes based on Δ0\Delta_0Δ0​ value is : I. [Mn(CN)6]3−[\text{Mn}(\text{CN})_6]^{3-}[Mn(CN)6​]3− II. [Co(CN)6]4−[\text{Co}(\text{CN})_6]^{4-}[Co(CN)6​]4− III. [Fe(CN)6]4−[\text{Fe}(\text{CN})_6]^{4-}[Fe(CN)6​]4− IV. [Fe(CN)6]3−[\text{Fe}(\text{CN})_6]^{3-}[Fe(CN)6​]3−
  1. A
    I < II < IV < III
  2. B
    IV < III < II < I
  3. C
    III < II < IV < I
  4. D
    II < III < I < IV
View written solutionFree

Correct answer: $\BOXED{\TEXT{I} < \TEXT{III} < \TEXT{II} < \TEXT{IV}}$, STORED ANSWER A APPEARS INCORRECT BECAUSE FOR THE SAME LIGAND, $\DELTA_O(\TEXT{FE}^{3+}) > \DELTA_O(\TEXT{FE}^{2+})$, SO IV MUST COME AFTER III, NOT BEFORE IT.

  1. Identify oxidation state and d-electron count

All complexes are octahedral with strong field ligand CN−\text{CN}^-CN−. We compare their octahedral crystal field splitting Δo\Delta_oΔo​.

  • I. [Mn(CN)6]3−[\text{Mn}(\text{CN})_6]^{3-}[Mn(CN)6​]3−

    Let oxidation state of Mn be xxx: x+6(−1)=−3⇒x=+3x+6(-1)=-3 \Rightarrow x=+3x+6(−1)=−3⇒x=+3 So Mn is Mn3+\text{Mn}^{3+}Mn3+, i.e. 3d43d^43d4.

  • II. [Co(CN)6]4−[\text{Co}(\text{CN})_6]^{4-}[Co(CN)6​]4− x+6(−1)=−4⇒x=+2x+6(-1)=-4 \Rightarrow x=+2x+6(−1)=−4⇒x=+2 So Co is Co2+\text{Co}^{2+}Co2+, i.e. 3d73d^73d7.

  • III. [Fe(CN)6]4−[\text{Fe}(\text{CN})_6]^{4-}[Fe(CN)6​]4− x+6(−1)=−4⇒x=+2x+6(-1)=-4 \Rightarrow x=+2x+6(−1)=−4⇒x=+2 So Fe is Fe2+\text{Fe}^{2+}Fe2+, i.e. 3d63d^63d6.

  • IV. [Fe(CN)6]3−[\text{Fe}(\text{CN})_6]^{3-}[Fe(CN)6​]3− x+6(−1)=−3⇒x=+3x+6(-1)=-3 \Rightarrow x=+3x+6(−1)=−3⇒x=+3 So Fe is Fe3+\text{Fe}^{3+}Fe3+, i.e. 3d53d^53d5.

  1. Use the trend of Δo\Delta_oΔo​

For a given ligand, Δo\Delta_oΔo​ generally:

  • increases with increasing oxidation state of the metal,
  • increases across the period from left to right for 3d metals.

Since all ligands are the same (CN−\text{CN}^-CN−), compare mainly using metal ion identity and oxidation state.

  1. Pairwise comparison
  • Between III and IV: [Fe(CN)6]3− has Fe3+>Fe2+[\text{Fe}(\text{CN})_6]^{3-} \text{ has Fe}^{3+} > \text{Fe}^{2+}[Fe(CN)6​]3− has Fe3+>Fe2+ so Δo(IV)>Δo(III)\Delta_o(\text{IV}) > \Delta_o(\text{III})Δo​(IV)>Δo​(III)

  • Between I and IV: Both are +3+3+3 oxidation state, but Fe is to the right of Mn in the 3d series, so Δo(IV)>Δo(I)\Delta_o(\text{IV}) > \Delta_o(\text{I})Δo​(IV)>Δo​(I)

  • Between III and II: Both are +2+2+2 oxidation state, but Co is to the right of Fe, so Δo(II)>Δo(III)\Delta_o(\text{II}) > \Delta_o(\text{III})Δo​(II)>Δo​(III)

  1. Construct overall increasing order

Thus the order becomes I<III<II<IV\text{I} < \text{III} < \text{II} < \text{IV}I<III<II<IV

  1. Match with the given options

The derived order is: [Mn(CN)6]3−<[Fe(CN)6]4−<[Co(CN)6]4−<[Fe(CN)6]3−[\text{Mn}(\text{CN})_6]^{3-} < [\text{Fe}(\text{CN})_6]^{4-} < [\text{Co}(\text{CN})_6]^{4-} < [\text{Fe}(\text{CN})_6]^{3-}[Mn(CN)6​]3−<[Fe(CN)6​]4−<[Co(CN)6​]4−<[Fe(CN)6​]3−

This order is not present exactly in the options.

Now check the stored answer A: I<II<IV<III\text{I} < \text{II} < \text{IV} < \text{III}I<II<IV<III This would imply Δo(IV)<Δo(III)\Delta_o(\text{IV}) < \Delta_o(\text{III})Δo​(IV)<Δo​(III), i.e. Fe3+^{3+}3+ has smaller splitting than Fe2+^{2+}2+ for the same ligand, which is incorrect.

Hence the stored answer does not agree with crystal field trends.

  1. Conclusion

The correct increasing order based on Δo\Delta_oΔo​ should be: I<III<II<IV\boxed{\text{I} < \text{III} < \text{II} < \text{IV}}I<III<II<IV​

Since no option matches exactly, the stored answer appears incorrect.

PreviousNext

More from Coordination Compounds

  • The calculated spin-only magnetic moments of K3​[Fe(OH)6​] and K4​[Fe(OH)6​] respectively are :2025 · MCQ
  • Consider the following low-spin complexes K3​[Co(NO2​)6​],K4​[Fe(CN)6​],K3​[Fe(CN)6​],Cu2​[Fe(CN)6​] and Zn2​[Fe(CN)6​]…2025 · Numerical
  • Identify the homoleptic complexes with odd number of d electrons in the central metal : (A) [FeO4​]2−(B) [Fe(CN)6​]3−(C) $\left[\mathrm{Fe}(\mathrm{CN})_5…2025 · MCQ
  • Given below are two statements : Statement (I) : A solution of [Ni(H2​O)6​]2+ is green in colour. Statement (II) : A solution of [Ni(CN)4​]2− is…2024 · MCQ
  • Which of the following complex is homoleptic?2024 · MCQ
  • Which of the following compounds show colour due to d-d transition?2024 · MCQ
  • [Co(NH3​)6​]3+ and [CoF6​]3− are respectively known as :2024 · MCQ
  • Given below are two statements : Statement (I) : Dimethyl glyoxime forms a six-membered covalent chelate when treated with NiCl2​ solution in presence of NH4​OH. Statement (II) : Prussian blue precipitate…2024 · MCQ