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प्रश्न
Why are different colours observed in octahedral and tetrahedral complexes for the same metal and same ligands?
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उत्तर
Lower wavelength is absorbed in octahedral complex than tetrahedral complex for the same metal and ligand. In tetrahedral coordination entity, formation of the d-orbital splitting is inverted and is smaller as compared to the octahedral field splitting. For the same metal-ligand complexes, it can be shown that
`Δ_t = (4/9)Δ_0`.
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संबंधित प्रश्न
On the basis of crystal field theory, write the electronic configuration for d4 ion if Δ0 > P.
State the superiority of crystal field theory over valence bond theory.
Why are low spin tetrahedral complexes rarely observed?
Write the electronic configuration of Fe(III) on the basis of crystal field theory when it forms an octahedral complex in the presence of (i) strong field, and (ii) weak field ligand. (Atomic no.of Fe=26)
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, \[\ce{[Co(NH3)6]^{3+}}\], \[\ce{[Co(CN)6]^{3-}}\], \[\ce{[Co(H2O)6]^{3+}}\]
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.
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:
\[\ce{[FeF6]^{3-}, [Fe(H2O)6]^{2+}, [Fe(CN)6]^{4-}}\]
The correct order of increasing crystal field strength in following series:
The magnitude of CFSE depends upon ______
The CFSE of [CoCl6]3– is 18000 cm–1 the CFSE for [CoCl4]– will be ______.
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:
- Both the complexes can be high spin.
- Ni(II) complex can very rarely below spin.
- With strong field Ligands, Mn(II) complexes can be low spin.
- 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 ______.
The value of the spin only magnetic moment for one of the following configurations is 2.84 BM. The correct one is:
