MCQEasyJEE 2026Crystal Field Theory

JEE Chemistry 2026 Question with Solution

The wavelength of light absorbed for the following complexes are in the order

[Co(NH3_3)6_6]3+^{3+} (I), [Co(H2_2O)6_6]3+^{3+} (II), [Co(CN)6_6]3^{3-} (III), [Co(NH3_3)5_5(H2_2O)]3+^{3+} (IV), [CoF6_6]3^{3-} (V)

  • A

    III << I << IV << II << V

  • B

    III << I << II << IV << V

  • C

    III << IV << I << II << V

  • D

    III << I << IV << V << II

Answer

Correct answer:A

Step-by-step solution

Standard Method

Given: The complexes are [Co(NH3_3)6_6]3+^{3+} (I), [Co(H2_2O)6_6]3+^{3+} (II), [Co(CN)6_6]3^{3-} (III), [Co(NH3_3)5_5(H2_2O)]3+^{3+} (IV), [CoF6_6]3^{3-} (V).

Find: The correct order of wavelength of light absorbed.

Concept: The wavelength of light absorbed is inversely proportional to the crystal field splitting energy Δo\Delta_o. Stronger field ligands produce larger splitting and therefore shorter absorbed wavelength.

The ligand field strength order is:

CN>NH3>H2O>F\text{CN}^- > \text{NH}_3 > \text{H}_2\text{O} > \text{F}^-

So, [Co(CN)6_6]3^{3-} has the maximum splitting and absorbs the shortest wavelength, while [CoF6_6]3^{3-} has the minimum splitting and absorbs the longest wavelength.

Also, [Co(NH3_3)5_5(H2_2O)]3+^{3+} lies between [Co(NH3_3)6_6]3+^{3+} and [Co(H2_2O)6_6]3+^{3+} in crystal field splitting.

Hence, the order of absorbed wavelength is:

III<I<IV<II<V\text{III} < \text{I} < \text{IV} < \text{II} < \text{V}

Therefore, the correct option is A.

Ligand Strength Comparison

Given: Absorption wavelength depends on octahedral crystal field splitting.

Find: Arrange the complexes in increasing order of absorbed wavelength.

For the same metal ion oxidation state, stronger ligands create larger Δo\Delta_o. Since absorbed energy is proportional to Δo\Delta_o and energy is inversely proportional to wavelength, larger Δo\Delta_o means shorter wavelength.

Thus we compare ligands using the spectrochemical series:

CN>NH3>H2O>F\text{CN}^- > \text{NH}_3 > \text{H}_2\text{O} > \text{F}^-

Therefore:

  1. [Co(CN)6_6]3^{3-} gives the shortest wavelength.
  2. [Co(NH3_3)6_6]3+^{3+} comes next.
  3. [Co(NH3_3)5_5(H2_2O)]3+^{3+} has one \text{H}_2\text{O replacing NH3\text{NH}_3, so its splitting is slightly less than (I) and wavelength is slightly larger.
  4. [Co(H2_2O)6_6]3+^{3+} absorbs at still longer wavelength.
  5. [CoF6_6]3^{3-} absorbs at the longest wavelength.

So the final order is:

III<I<IV<II<V\text{III} < \text{I} < \text{IV} < \text{II} < \text{V}

Hence, A is correct.

Common mistakes

  • Assuming stronger ligands absorb longer wavelength light. This is wrong because stronger ligands increase Δo\Delta_o, so the absorbed energy increases and the wavelength decreases. Compare ligand strength first, then invert the order for wavelength.

  • Ignoring the mixed-ligand complex [Co(NH3_3)5_5(H2_2O)]3+^{3+}. This is wrong because its splitting must lie between the all-ammine and all-aqua complexes. Place it between (I) and (II).

  • Using an incorrect spectrochemical series such as placing H2O\text{H}_2\text{O} above NH3\text{NH}_3. This gives the wrong order of crystal field splitting. Use CN>NH3>H2O>F\text{CN}^- > \text{NH}_3 > \text{H}_2\text{O} > \text{F}^-.

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