Advertisements
Advertisements
प्रश्न
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 |
विकल्प
A - (3), B - (1), C - (5), D - (2)
A - (4), B - (3), C - (2), D - (1)
A - (3), B - (2), C - (4), D - (1)
A - (4), B - (1), C - (2), D - (3)
Advertisements
उत्तर
A - (3), B - (1), C - (5), D - (2)
Explanation:
| Column I (Complex ion) | Column II (Hybridisation, number of unpaired electrons) |
| A. \[\ce{[Cr(H2O)6]^{3+}}\] | 3. d2sp3, 3 |
| B. \[\ce{[Co(CN)4]^{2-}}\] | 1. dsp2, 1 |
| C. \[\ce{[Ni(NH3)6]^{2+}}\] | 5. sp3d2, 2 |
| D. \[\ce{[MnF6]^{4-}}\] | 2. sp3d2, 5 |
APPEARS IN
संबंधित प्रश्न
On the basis of crystal field theory, write the electronic configuration for d4 ion if ∆0 < P.
Draw figure to show the splitting of d orbitals in an octahedral crystal field.
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)
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 ______.
Why are low spin tetrahedral complexes not formed?
Give the electronic configuration of the following complexes on the basis of Crystal Field Splitting theory.
\[\ce{[CoF6]^{3-}, [Fe(CN)6]^{4-} and [Cu(NH3)6]^{2+}}\].
\[\ce{CuSO4 . 5H2O}\] 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:-
Using crystal field theory, write the electronic configuration of d5 ion, if Δ0 > P.
For octahedral Mn(II) and tetrahedral Ni(II) complexes, consider the following statements:
- Both the complexes can be high spin.
- Ni(II) complex can very rarely below spin.
- With strong field Ligands, Mn(II) complexes can be low spin.
- Aqueous solution of Mn (II) ions is yellow in colour.
The correct statements 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.
On the basis of crystal field theory, write the electronic configuration for d4 with a strong field ligand for which Δ0 > P.
