मराठी

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 - Chemistry

Advertisements
Advertisements

प्रश्न

 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) 

बेरीज
Advertisements

उत्तर

Atomic no. of Fe = 26

`"Fe"= ["Ar"]3"d"^6  4"s"^2`  

`"Fe"^{3+} = ["Ar"]3"d"^6 4"s"^2` 

`"Fe"^(+3) = ["AR"] 3"d"^5 4"s"^0`

In octahedral crystal field.

(i) Strong field ligand - Electrons will be paired.

No. of unpaired e- = 1
Paramagnetic 
`μ = sqrt(n(n+2) = sqrt(1(3) = sqrt3 B.M`
(ii) Weak field ligand  
- Electrons follow Hund’s rule 

No. of unpaired = 5 
Paramagnetic 
`μ =sqrt(5(5+2))= sqrt(35)  B.M.`

shaalaa.com
  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
2018-2019 (March) 56/3/2

व्हिडिओ ट्यूटोरियलVIEW ALL [1]

संबंधित प्रश्‍न

How are the following conversions carried out?

Benzoic acid into metanitrobenzoic acid.


Why are low spin tetrahedral complexes rarely observed?


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


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.


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:

\[\ce{[CoF6]^{3-}, [Co(H2O)6]^{2+}, [Co(Cn)6]^{3-}}\]


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.


Considering crystal field theory, strong-field ligands such as CN:


What is crystal field splitting energy?


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 ______.


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+

Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×