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कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

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: [FeFX6]X3−,[Fe(HX - Chemistry

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प्रश्न

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:

\[\ce{[FeF6]^{3-}, [Fe(H2O)6]^{2+}, [Fe(CN)6]^{4-}}\]

दीर्घउत्तर
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उत्तर

(1) \[\ce{FeF^{3-}6}\]:

\[\ce{Fe^{3+} = 3d^5}\]

Number of unpaired electrons = 5

Magnetic moment = `sqrt(5(5 + 2))` = 5.92 BM

(2) \[\ce{[Fe(H2O)6]^{2+}}\]:

\[\ce{Fe^{2+} = 3d^6}\]

Number of unpaired electrons = 4

Magnetic moment = `sqrt(4(4 + 2))` = 4.9 BM

(3) \[\ce{[Fe(CN)6]^{4-}}\]:

\[\ce{Fe^{2+} = 3d^6}\]

Since CN is a strong field ligand all the electrons get paired.

No unpaired electrons so diamagnetic.

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पाठ 9: Coordination Compounds - Exercises [पृष्ठ १२७]

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एनसीईआरटी एक्झांप्लर Chemistry [English] Class 12
पाठ 9 Coordination Compounds
Exercises | Q VI. 46. (ii) | पृष्ठ १२७

संबंधित प्रश्‍न

On the basis of crystal field theory, write the electronic configuration for d4 ion if ∆0 < P.


How are the following conversions carried out?

Benzoic acid into metanitrobenzoic acid.


Why are low spin tetrahedral complexes rarely observed?


The colour of the coordination compounds depends on the crystal field splitting. What will be the correct order of absorption of wavelength of light in the visible region, for the complexes, \[\ce{[Co(NH3)6]^{3+}}\], \[\ce{[Co(CN)6]^{3-}}\], \[\ce{[Co(H2O)6]^{3+}}\]


The CFSE for octahedral \[\ce{[CoCl6]^{4-}}\] is 18,000 cm–1. The CFSE for tetrahedral \[\ce{[CoCl4]^{2-}}\] will be ______.


Atomic number of \[\ce{Mn, Fe, Co}\] and Ni are 25, 26, 27 and 28 respectively. Which of the following outer orbital octahedral complexes have same number of unpaired electrons?

(i) \[\ce{[MnCl6]^{3-}}\]

(ii) \[\ce{[FeF6]^{3-}}\]

(iii) \[\ce{[CoF6]^{3-}}\]

(iv) \[\ce{[Ni(NH3)6]^{2+}}\]


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.


On the basis of crystal field theory explain why Co(III) forms paramagnetic octahedral complex with weak field ligands whereas it forms diamagnetic octahedral complex with strong field ligands.


Why are low spin tetrahedral complexes not formed?


In a coordination entity, the electronic configuration of the central metal ion is t2g3 eg

Draw the crystal field splitting diagram for the above complex.


Crystal field stabilising energy for high spind4 octahedral complex is:-


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


What is the difference between a weak field ligand and a strong field ligand?


What is crystal field splitting energy?


The correct order of intensity of colors of the compounds is ______.


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:


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


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