Advertisements
Advertisements
प्रश्न
The CFSE for octahedral \[\ce{[CoCl6]^{4-}}\] is 18,000 cm–1. The CFSE for tetrahedral \[\ce{[CoCl4]^{2-}}\] will be ______.
विकल्प
18,000 cm–1
16,000 cm–1
8,000 cm–1
20,000 cm–1
Advertisements
उत्तर
The CFSE for octahedral \[\ce{[CoCl6]^{4-}}\] is 18,000 cm–1. The CFSE for tetrahedral \[\ce{[CoCl4]^{2-}}\] will be 8,000 cm–1.
Explanation:
CFSE for octahedral and tetrahedral complex is related as
`Δ^t = 4/9 Δ_o`
Where `Δ_o` = CFSE for octahedral complex
`Δ_o` = CFSE for tetrahedral complex
`Δ_o` = 18000 cm–1
`Δ_t = 4/9 xx 18000` = 8000 cm–1
APPEARS IN
संबंधित प्रश्न
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.
Why are low spin tetrahedral complexes rarely observed?
Draw the structures of the following :
(1) XeF6
(2) IF7
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, \[\ce{[Co(NH3)6]^{3+}}\], \[\ce{[Co(CN)6]^{3-}}\], \[\ce{[Co(H2O)6]^{3+}}\]
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.
\[\ce{CuSO4 . 5H2O}\] is blue in colour while \[\ce{CuSO4}\] is colourless. Why?
In a coordination entity, the electronic configuration of the central metal ion is t2g3 eg1
Draw the crystal field splitting diagram for the above complex.
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 ______
What is the spectrochemical series?
What is the difference between a weak field ligand and a strong field ligand?
The correct order of intensity of colors of the compounds is ______.
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 ______.
On the basis of crystal field theory, write the electronic configuration for d4 with a strong field ligand for which Δ0 > P.
On the basis of Crystal Field Theory, write the electronic configuration of d4 ion if Δ0 > P.
