हिंदी
कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

What is crystal field splitting energy?

Advertisements
Advertisements

प्रश्न

What is crystal field splitting energy?

अति संक्षिप्त उत्तर
Advertisements

उत्तर

The energy difference between the two sets of degenerate orbitals (t2g and eg) after crystal field splitting is known as the crystal field splitting energy. It is denoted by Δo.

shaalaa.com
  क्या इस प्रश्न या उत्तर में कोई त्रुटि है?
अध्याय 5: Coordinate Compounds - Exercises [पृष्ठ १३९]

APPEARS IN

एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
अध्याय 5 Coordinate Compounds
Exercises | Q 5.18 (i) | पृष्ठ १३९
सामाचीर कलवी Chemistry - Volume 1 and 2 [English] Class 12 TN Board
अध्याय 5 Coordination Chemistry
Evaluation | Q 18. | पृष्ठ १७२
नूतन Chemistry [English] Class 12 ISC
अध्याय 5 Coordination Compounds
'NCERT TEXT-BOOK' Exercises | Q 9.18 (i) | पृष्ठ ५५९

संबंधित प्रश्न

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


How does the magnitude of Δo decide the actual configuration of d orbitals in a coordination entity?


How are the following conversions carried out?

Benzoic acid into metanitrobenzoic acid.


Why are low spin tetrahedral complexes rarely observed?


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


An aqueous pink solution of cobalt (II) chloride changes to deep blue on addition of excess of HCl. This is because:

(i) \[\ce{[Co(H2O)6]^{2+}}\] is transformed into \[\ce{[CoCl6]}^{4-}\]

(ii) \[\ce{[Co(H2O)6]^{2+}}\] is transformed into \[\ce{[CoCl4]}^{2-}\]

(iii) tetrahedral complexes have smaller crystal field splitting than octahedral complexes.

(iv) tetrahedral complexes have larger crystal field splitting than octahedral complex.


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

Why are different colours observed in octahedral and tetrahedral complexes for the same metal and same ligands?


Crystal field stabilising energy for high spind4 octahedral complex is:-


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:

  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 ______.


The complex that has highest crystal field splitting energy (Δ) is ______.


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.


Read the passage carefully and answer the questions that follow.

Crystal field splitting by various ligands

Metal complexes show different colours due to d-d transitions. The complex absorbs light of specific wavelength to promote the electron from t2g to eg level. The colour of the complex is due to the transmitted light, which is complementary of the colour absorbed.

The wave number of light absorbed by different complexes of Cr ion are given below:

Complex Wavenumber of light absorbed (cm-1) Energy of light absorbed (kJ/mol)
[CrA6]3- 13,640 163
[CrB6]3+ 17,830 213
[CrC6]3+ 21,680 259
[CrD6]3- 26,280 314

Answer the following questions:

(a) Out of ligands "A", "B", "C" and "D", which ligand causes maximum crystal field splitting? Why?

OR

Which of the two, “A” or “D” will be a weak field ligand? Why?

(b) Which of the complexes will be violet in colour? [CrA6]3- or [CrB6]3+ and why?
(Given: If 560 - 570 nm of light is absorbed, the colour of the complex observed is violet.)

(c) If the ligands attached to Cr3+ ion in the complexes given in the table above are water, cyanide ion, chloride ion, and ammonia (not in this order).

Identify the ligand, write the formula and IUPAC name of the following:

  1. [CrA6]3-
  2. [CrC6]3+

The correct order of the wavelength of light absorbed by the following complexes is:

  1. [Co(NH3)6]3+
  2. [Co(CN)6]3−
  3. [Cu(H2O)4]2+
  4. [Ti(H2O)6]3+

Choose the correct answer from the options given below:


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×