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How does the magnitude of Δo decide the actual configuration of d orbitals in a coordination entity?

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प्रश्न

How does the magnitude of Δo decide the actual configuration of d orbitals in a coordination entity?

लघु उत्तरीय
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उत्तर

  1. If Δ0 < P, the fourth electron enters one of the eg orbitals giving the configuration \[\ce{t^3_{2g}e^1_g}\]. Ligands for which Δ0 < P are known as weak field ligands and form high spin complexes.
  2. If Δ0 > P, it becomes more energetically favourable for the fourth electron to occupy a t2g orbital with configuration \[\ce{t^4_{2g}e^0_g}\]. Ligands which produce this effect are known as strong field ligands and form low spin complexes.
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अध्याय 5: Coordinate Compounds - Exercises [पृष्ठ १३९]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
अध्याय 5 Coordinate Compounds
Exercises | Q 5.18 (ii) | पृष्ठ १३९
नूतन Chemistry [English] Class 12 ISC
अध्याय 5 Coordination Compounds
'NCERT TEXT-BOOK' Exercises | Q 9.18 (ii) | पृष्ठ ५५९

संबंधित प्रश्न

On the basis of crystal field theory, write the electronic configuration for d4 ion if Δ0 > P.


How are the following conversions carried out?

Benzoic acid into metanitrobenzoic acid.


State the superiority of crystal field theory over valence bond theory.


Complete and balance the following reactions:

\[\ce{P4 + H2SO4 ->}\] ______ + ______ + ______


An aqueous pink solution of cobalt (II) chloride changes to deep blue on addition of excess of HCl. This is because:

(i) \[\ce{[Co(H2O)6]^{2+}}\] is transformed into \[\ce{[CoCl6]}^{4-}\]

(ii) \[\ce{[Co(H2O)6]^{2+}}\] is transformed into \[\ce{[CoCl4]}^{2-}\]

(iii) tetrahedral complexes have smaller crystal field splitting than octahedral complexes.

(iv) tetrahedral complexes have larger crystal field splitting than octahedral complex.


Why are low spin tetrahedral complexes not formed?


Give the electronic configuration of the following complexes on the basis of Crystal Field Splitting theory.

\[\ce{[CoF6]^{3-}, [Fe(CN)6]^{4-} and [Cu(NH3)6]^{2+}}\].


Arrange following complex ions in increasing order of crystal field splitting energy (∆O):

\[\ce{[Cr(Cl)6]^{3-}, [Cr(CN)6]^{3-}, [Cr(NH3)6]^{3+}}\].


Using crystal field theory, draw energy level diagram, write electronic configuration of the central metal atom/ion and determine the magnetic moment value in the following:

\[\ce{[CoF6]^{3-}, [Co(H2O)6]^{2+}, [Co(Cn)6]^{3-}}\]


[Ni(H2O)6]2+ (aq) is green in colour whereas [Ni(H2O)4 (en)]2+ (aq)is blue in colour, give reason in support of your answer.


Considering crystal field theory, strong-field ligands such as CN–:


The CFSE of [CoCl6]3– is 18000 cm–1 the CFSE for [CoCl4]– will be ______.


Using crystal field theory, write the electronic configuration of d5 ion, if Δ0 > P.


What is crystal field splitting energy?


For octahedral Mn(II) and tetrahedral Ni(II) complexes, consider the following statements:

  1. Both the complexes can be high spin.
  2. Ni(II) complex can very rarely below spin.
  3. With strong field Ligands, Mn(II) complexes can be low spin.
  4. Aqueous solution of Mn (II) ions is yellow in colour.

The correct statements are:


Consider that d6 metal ion (M2+) forms a complex with aqua ligands and the spin only magnetic moment of the complex is 4.90 BM. The geometry and the crystal field stabilization energy of the complex are ______.


The complex that has highest crystal field splitting energy (Δ) is ______.


Read the passage carefully and answer the questions that follow.

Crystal field splitting by various ligands

Metal complexes show different colours due to d-d transitions. The complex absorbs light of specific wavelength to promote the electron from t2g to eg level. The colour of the complex is due to the transmitted light, which is complementary of the colour absorbed.

The wave number of light absorbed by different complexes of Cr ion are given below:

Complex Wavenumber of light absorbed (cm-1) Energy of light absorbed (kJ/mol)
[CrA6]3- 13,640 163
[CrB6]3+ 17,830 213
[CrC6]3+ 21,680 259
[CrD6]3- 26,280 314

Answer the following questions:

(a) Out of ligands "A", "B", "C" and "D", which ligand causes maximum crystal field splitting? Why?

OR

Which of the two, “A” or “D” will be a weak field ligand? Why?

(b) Which of the complexes will be violet in colour? [CrA6]3- or [CrB6]3+ and why?
(Given: If 560 - 570 nm of light is absorbed, the colour of the complex observed is violet.)

(c) If the ligands attached to Cr3+ ion in the complexes given in the table above are water, cyanide ion, chloride ion, and ammonia (not in this order).

Identify the ligand, write the formula and IUPAC name of the following:

  1. [CrA6]3-
  2. [CrC6]3+

The value of the spin only magnetic moment for one of the following configurations is 2.84 BM. The correct one is:


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