Advertisements
Advertisements
प्रश्न
State the superiority of crystal field theory over valence bond theory.
Why is crystal field theory regarded superior to valence bond theory?
Advertisements
उत्तर
Despite the constraints mentioned above, crystal field theory outperforms valence bond theory. The crystal field theory is thought to be preferable to the valence bond theory for the following reasons.
- Crystal field theory describes the magnetic properties of complexes in detail and provides an explanation for how magnetic moments vary with temperature. VBT fails to provide these additional details.
- Crystal field theory measures the stability of a complex. With this measure, the geometry gained by a particular complex can be predicted. VBT does not include such a measure.
- Crystal field theory explains certain thermodynamic and kinetic features of complexes. VBT does not offer such an explanation.
- Only crystal field theory can explain the observed d-d transitions in complexes and their hue. The VBT does not explain spectroscopic features or complex coloration adequately.
APPEARS IN
संबंधित प्रश्न
On the basis of crystal field theory, write the electronic configuration for d4 ion if Δ0 > P.
Draw figure to show the splitting of d orbitals in an octahedral crystal field.
How are the following conversions carried out?
Benzoic acid into metanitrobenzoic acid.
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, \[\ce{[Co(NH3)6]^{3+}}\], \[\ce{[Co(CN)6]^{3-}}\], \[\ce{[Co(H2O)6]^{3+}}\]
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) \[\ce{[Fe(CN)6]^{3-}}\]
Why are low spin tetrahedral complexes not formed?
Give the electronic configuration of the following complexes on the basis of Crystal Field Splitting theory.
\[\ce{[CoF6]^{3-}, [Fe(CN)6]^{4-} and [Cu(NH3)6]^{2+}}\].
Arrange following complex ions in increasing order of crystal field splitting energy (∆O):
\[\ce{[Cr(Cl)6]^{3-}, [Cr(CN)6]^{3-}, [Cr(NH3)6]^{3+}}\].
\[\ce{CuSO4 . 5H2O}\] is blue in colour while \[\ce{CuSO4}\] is colourless. Why?
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:
\[\ce{[CoF6]^{3-}, [Co(H2O)6]^{2+}, [Co(Cn)6]^{3-}}\]
[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.
Considering crystal field theory, strong-field ligands such as CN–:
The correct order of increasing crystal field strength in following series:
Crystal field stabilising energy for high spind4 octahedral complex is:-
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 ______.
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 the d5 ion with a strong field ligand for which Δ0 > P.
Read the passage carefully and answer the questions that follow.
|
Crystal field splitting by various ligands Metal complexes show different colours due to d-d transitions. The complex absorbs light of specific wavelength to promote the electron from t2g to eg level. The colour of the complex is due to the transmitted light, which is complementary of the colour absorbed. The wave number of light absorbed by different complexes of Cr ion are given below:
|
Answer the following questions:
(a) Out of ligands "A", "B", "C" and "D", which ligand causes maximum crystal field splitting? Why?
OR
Which of the two, “A” or “D” will be a weak field ligand? Why?
(b) Which of the complexes will be violet in colour? [CrA6]3- or [CrB6]3+ and why?
(Given: If 560 - 570 nm of light is absorbed, the colour of the complex observed is violet.)
(c) If the ligands attached to Cr3+ ion in the complexes given in the table above are water, cyanide ion, chloride ion, and ammonia (not in this order).
Identify the ligand, write the formula and IUPAC name of the following:
- [CrA6]3-
- [CrC6]3+
On the basis of Crystal Field Theory, write the electronic configuration of d4 ion if Δ0 > P.
