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Why are low spin tetrahedral complexes not formed?

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प्रश्न

Why are low spin tetrahedral complexes not formed?

अति संक्षिप्त उत्तर
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उत्तर

For tetrahedral complexes, the crystal field splitting energy is too low. It is lower than the pairing energy, so the pairing of electrons is not favoured, and therefore the complexes cannot form low-spin complexes.

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अध्याय 9: Coordination Compounds - Exercises [पृष्ठ १२४]

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एनसीईआरटी एक्झांप्लर Chemistry Exemplar [English] Class 12
अध्याय 9 Coordination Compounds
Exercises | Q III. 29. | पृष्ठ १२४

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.


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


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


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.


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

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


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

The CFSE for octahedral [CoCl6]−4 is 18,000 cm−1. What will be the CFSE for tetrahedral [CoCl3]−2?


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


The correct order of increasing crystal field strength in following series:


The magnitude of CFSE depends upon ______


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?


What is crystal field splitting energy?


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 ______.


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


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