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प्रश्न
Choose the correct statement.
पर्याय
Square planar complexes are more stable than octahedral complexes
The spin only magnetic moment of \[\ce{[Cu(Cl)4]^2-}\] is 1.732 BM and it has square planar structure.
Crystal field splitting energy (Δ0) of \[\ce{[FeF6]^4-}\] is higher than the (Δ0) of \[\ce{[Fe(CN)6]^4-}\]
Crystal field stabilization energy of \[\ce{[V(H2O)6]^2+}\] is higher than the crystal field stabilization of \[\ce{[Ti(H2O)6]^2+}\]
उत्तर
Crystal field stabilization energy of \[\ce{[V(H2O)6]^2+}\] is higher than the crystal field stabilization of \[\ce{[Ti(H2O)6]^2+}\]
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संबंधित प्रश्न
The sum of primary valence and secondary valence of the metal M in the complex [M(en)2(Ox)]Cl is ____________.
Crystal field stabilization energy for high spin d5 octahedral complex is ____________.
Arrange the following in order of increasing molar conductivity.
i) \[\ce{Mg[Cr(NH3) (Cl)5]}\]
ii) \[\ce{[Cr(NH3)5 Cl]3 [CoF6]2}\]
iii) \[\ce{[Cr(NH3)3 Cl3]}\]
Give an example for a complex of the type [Ma2b2c2] where a, b, c are monodentate ligands and give the possible isomers.
Give one test to differentiate \[\ce{[Co(NH3)5Cl]SO4}\] and \[\ce{[Co(NH3)5SO4]Cl}\].
Why tetrahedral complexes do not exhibit geometrical isomerism.
What is crystal field splitting energy?
A solution of \[\ce{[Ni(H2O)6]^2+}\] is green, whereas a solution of \[\ce{[Ni(CN)4]^2-}\] is colorless – Explain.
Discuss briefly the nature of bonding in metal carbonyls.
Write the oxidation state, coordination number, nature of ligand, magnetic property and electronic configuration in octahedral crystal field for the complex \[\ce{K4[Mn(CN)6]}\].
