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Coordination Co...

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  • Question 1
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    In an octahedral complex, if ligands on one axis are displaced little away from their ideal positions, the crystal field splitting of d-orbitals for this complex is as given below
    $$d_{x^2-y^2} d_{z^2} d_{xy} d_{yz} d_{xz}$$
    The ligands are displaced on which axis/ axes :

  • Question 2
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    Which of the following statement(s) is/are not correct?

  • Question 3
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    The magnitude of crystal field stabilization energy in octahedral field depends on
    I : the nature of the ligand
    II : the charge on the metal ion
    III : whether the metal is in the first, second or third row of the transition elements.

  • Question 4
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    Coordination compounds have great importance in biological systems. In this context which of the following statement(s) is/are incorrect?

  • Question 5
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    Which of the following statements are true regarding Werner's theory are true?
    $$( 1 )$$ Ligands are connected to the metal ions by covalent bonds
    $$( 2 )$$ Secondary valencies have directional properties
    $$( 3 )$$ Secondary valencies are non- ionizable

  • Question 6
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    The IUPAC name for the complex $$\displaystyle \left [ Co\left ( NH_{3} \right )_{5}\left ( NO_{2} \right ) \right ]Cl_{2}$$ is:

  • Question 7
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    Directions For Questions

    The crystal field theory (C.F.T.) is now much more widely accepted than the valence bond theory. It assume that the attraction between the central metal and the ligands in a complex is purely electrostatic. According to C.F.T. ligands are treated as a point charge and crystal field splitting energy (CFSE) increases the thermodynamic stability of the complexes. Value of CFSE depends upon nature of ligand and a spectrochemical series has been made experimentally. For tetrahedral complexes, $$\Delta$$  is about 4/9 times to $$\Delta _{0}$$ (CFSE for octahedral complexes.) This energy lies in visible region and i.e. why electronic transition are responsible for colour.

    ...view full instructions

    Which of the following statement is not correct about C.F.T.?

  • Question 8
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    Which one of the following pairs of isomers and types of isomerism are correctly matched?
    (i) $$[Co(NH_{3})_{5}(NO_{2})]Cl_{2}$$ and $$[Co(NH_{3})_{5}(ONO)Cl_{2} ... (Linkage)$$
    (ii) $$[Cu(NH_{3})_{4}][PtCl_{4}]$$ and $$[Pt(NH_{3})_{4}][CuCl_{4}] ... (Coordination)$$
    (iii) $$[PtCl_{2}(NH_{3})_{4}]Br_{2}$$ and $$[PtBr_{2}(NH_{3})_{4}]Cl_{2} ... (Ionization)$$
    Select the correct answer using the codes given below:

  • Question 9
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    The degeneracy of $$d-orbitals$$ is lost under:
    (I) Strong field ligand (II) Weak field ligand (III) Mixed field ligand (IV) Chelated ligand field
    Choose the correct code.

  • Question 10
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    Match List-I with List-II and select the correct answer using the codes given below:

    List IList II
    (I) $$[FeF_{6}]^{3-}$$(A) $$1.73\ BM$$
    (II) $$[Ti(H_{2}O)_{6}]^{3+}$$(B) $$5.93\ BM$$
    (III) $$[Cr(NH_{3})_{6}]^{3+}$$(C) $$0.00\ BM$$
    (IV) $$[Ni(H_{2}O)_{6}]^{2+}$$(D) $$2.83\ BM$$
    (V) $$[Fe(CN)_{6}]^{4-}$$(E) $$3.88\ BM$$

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