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The hexaquo manganese (II) ion contains five unpaired electrons, while the hexacyanoion contains only one unpaired electron. Explain using Crystal Field Theory. - Chemistry

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प्रश्न

The hexaquo manganese (II) ion contains five unpaired electrons, while the hexacyanoion contains only one unpaired electron. Explain using Crystal Field Theory.

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उत्तर

The configuration of Mn in oxidation state +2 is 3d5. In the presence of H2O (weak field ligand) as ligand, the distribution of these five electrons is \[\ce{t^3_{2{g}} e^2_{{g}}}\] i.e. all the electrons remain unpaired. In the presence of CN (strong field ligand) as ligand, the distribution is \[\ce{t^5_{2{g}} e^0_{{g}}}\] i.e. two t2g orbitals have paired electrons while the third t2g orbital has one unpaired electron.

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अध्याय 9: Coordinate Compounds - Intext Questions [पृष्ठ २५४]

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एनसीईआरटी Chemistry [English] Class 12
अध्याय 9 Coordinate Compounds
Intext Questions | Q 10 | पृष्ठ २५४

संबंधित प्रश्न

On the basis of crystal field theory, write the electronic configuration for d4 ion if ∆0 < P.


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How are the following conversions carried out?

Benzoic acid into metanitrobenzoic acid.


 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) 


Complete and balance the following reactions:

(1) P4 + H2SO4 → ____ + _____ + _____ + _____
(2) Ag + HNO3(dilute) → _____ + ______ + _____ + _____


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.

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


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


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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 ______


The CFSE of [CoCl6]3– is 18000 cm–1 the CFSE for [CoCl4] will be ______.


What is the difference between a weak field ligand and a strong field ligand?


For octahedral Mn(II) and tetrahedral Ni(II) complexes, consider the following statements:

(i) Both the complexes can be high spin.

(ii) Ni(II) complex can very rarely below spin.

(iii) With strong field Ligands, Mn(II) complexes can be low spin.

(iv) 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 ______.


On the basis of crystal field theory, write the electronic configuration for d4 with a strong field ligand for which Δ0 > P.


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