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Atomic number of 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) [MnClX6]X3− (ii)

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प्रश्न

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) \[\ce{[Ni(NH3)6]^{2+}}\]

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उत्तर

(i) \[\ce{[MnCl6]^{3-}}\]

(iii) \[\ce{[CoF6]^{3-}}\]

Explanation:

\[\ce{[MnCl6]^{3-} : MN^{3+} (3d^4)}\]

`↑` `↑` `↑` `↑`  

\[\ce{[CoF6]^{3-} : Co^{3+} (3d^6)}\]

`↑↓` `↑` `↑` `↑` `↑`
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अध्याय 9: Coordination Compounds - Exercises [पृष्ठ १२२]

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एनसीईआरटी एक्झांप्लर Chemistry Exemplar [English] Class 12
अध्याय 9 Coordination Compounds
Exercises | Q II. 16. | पृष्ठ १२२

संबंधित प्रश्न

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.


State the superiority of crystal field theory over valence bond theory.


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, \[\ce{[Co(NH3)6]^{3+}}\], \[\ce{[Co(CN)6]^{3-}}\], \[\ce{[Co(H2O)6]^{3+}}\]


The CFSE for octahedral \[\ce{[CoCl6]^{4-}}\] is 18,000 cm–1. The CFSE for tetrahedral \[\ce{[CoCl4]^{2-}}\] will be ______.


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) \[\ce{[Fe(CN)6]^{3-}}\]


Match the complex ions given in Column I with the hybridisation and number of unpaired electrons given in Column II and assign the correct code:

Column I (Complex ion) Column II (Hybridisation, number of unpaired electrons)
A. \[\ce{[Cr(H2O)6]^{3+}}\] 1. dsp2, 1
B. \[\ce{[Co(CN)4]^{2-}}\] 2. sp3d2, 5
C. \[\ce{[Ni(NH3)6]^{2+}}\] 3. d2sp3, 3
D. \[\ce{[MnF6]^{4-}}\] 4. sp3, 4
  5. sp3d2, 2

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


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:

  1. Both the complexes can be high spin.
  2. Ni(II) complex can very rarely below spin.
  3. With strong field Ligands, Mn(II) complexes can be low spin.
  4. Aqueous solution of Mn (II) ions is yellow in colour.

The correct statements are:


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 weak ligand for which Δ0 < P.


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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