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Arrange following complex ions in increasing order of crystal field splitting energy (∆O): [Cr(Cl)X6]X3−,[Cr(CN)X6]X3−,[Cr(NHX3)X6]X3+. - Chemistry

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प्रश्न

Arrange following complex ions in increasing order of crystal field splitting energy (∆O):

\[\ce{[Cr(Cl)6]^{3-}, [Cr(CN)6]^{3-}, [Cr(NH3)6]^{3+}}\].

एक पंक्ति में उत्तर
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उत्तर

Crystal field splitting energy increases in the order:

[Cr(Cl)6]3– < [Cr(NH3)6]3+ < [Cr(CN)6]3−

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अध्याय 9: Coordination Compounds - Exercises [पृष्ठ १२४]

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एनसीईआरटी एक्झांप्लर Chemistry [English] Class 12
अध्याय 9 Coordination Compounds
Exercises | Q III. 32. | पृष्ठ १२४

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.


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


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


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

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


[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.


In a coordination entity, the electronic configuration of the central metal ion is t2g3 eg

Draw the crystal field splitting diagram for the above complex.


The correct order of increasing crystal field strength in following series:


The magnitude of CFSE depends upon ______


Using crystal field theory, write the electronic configuration of d5 ion, if Δ0 > P.


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 ______.


On the basis of Crystal Field theory, write the electronic configuration for the d5 ion with a strong field 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.


On the basis of Crystal Field Theory, write the electronic configuration of d4 ion if Δ0 > P.


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