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

What is crystal field splitting energy?

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प्रश्न

What is crystal field splitting energy?

अति संक्षिप्त उत्तर
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उत्तर

The energy difference between the two sets of degenerate orbitals (t2g and eg) after crystal field splitting is known as the crystal field splitting energy. It is denoted by Δ0.

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पाठ 5: Coordinate Compounds - Exercises [पृष्ठ १३९]

APPEARS IN

एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
पाठ 5 Coordinate Compounds
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सामाचीर कलवी Chemistry - Volume 1 and 2 [English] Class 12 TN Board
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Evaluation | Q 18. | पृष्ठ १७२
नूतन Chemistry [English] Class 12 ISC
पाठ 5 Coordination Compounds
'NCERT TEXT-BOOK' Exercises | Q 9.18 (i) | पृष्ठ ५५९

संबंधित प्रश्‍न

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


The hexaquo manganese(II) ion contains five unpaired electrons, while the hexacyanoion contains only one unpaired electron. Explain using Crystal Field Theory.


Draw figure to show the splitting of d orbitals in an octahedral crystal field.


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


Why are low spin tetrahedral complexes rarely observed?


Complete and balance the following reactions:

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


Atomic number of \[\ce{Mn}\], \[\ce{Fe}\] and \[\ce{Co}\] are 25, 26 and 27 respectively. Which of the following inner orbital octahedral complex ions are diamagnetic?

(i) \[\ce{[Co(NH3)6]^{3+}}\]

(ii) \[\ce{[Mn(CN)6]^{3-}}\] 

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

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


Match the complex ions given in Column I with the hybridisation and number of unpaired electrons given in Column II and assign the correct code:

Column I (Complex ion) Column II (Hybridisation, number of unpaired electrons)
A. \[\ce{[Cr(H2O)6]^{3+}}\] 1. dsp2, 1
B. \[\ce{[Co(CN)4]^{2-}}\] 2. sp3d2, 5
C. \[\ce{[Ni(NH3)6]^{2+}}\] 3. d2sp3, 3
D. \[\ce{[MnF6]^{4-}}\] 4. sp3, 4
  5. sp3d2, 2

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:

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


Why are different colours observed in octahedral and tetrahedral complexes for the same metal and same ligands?


[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.


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 the spectrochemical series?


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


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:


On the basis of crystal field theory, write the electronic configuration for the d5 ion with a weak ligand for which Δ0 < P.


On the basis of Crystal Field Theory, write the electronic configuration of d4 ion if Δ0 > P.


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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