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The hybridization of [CoF(6)]^(3-) and [...

The hybridization of `[CoF_(6)]^(3-)` and `[Co(C_(2)O_(4))}^(3-)` are :

A

both `sp^(3)d^(2)`

B

both `d^(2)sp^(3)`

C

`sp^(3)d^(2)` and `d^(2)sp^(3)` respectively

D

`d^(2)sp^(3)` and `sp^(3)d^(2)` respectively

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The correct Answer is:
To determine the hybridization of the complexes \([CoF_6]^{3-}\) and \([Co(C_2O_4)]^{3-}\), we will follow these steps: ### Step 1: Determine the oxidation state of cobalt in both complexes. 1. **For \([CoF_6]^{3-}\)**: - Let the oxidation state of cobalt be \(x\). - The oxidation state of fluorine (F) is \(-1\). - The overall charge of the complex is \(-3\). - Therefore, the equation is: \[ x + 6(-1) = -3 \implies x - 6 = -3 \implies x = +3 \] 2. **For \([Co(C_2O_4)]^{3-}\)**: - The oxalate ion \((C_2O_4)^{2-}\) has an overall charge of \(-2\). - Let the oxidation state of cobalt again be \(x\). - The overall charge of the complex is \(-3\). - Therefore, the equation is: \[ x + (-2) = -3 \implies x - 2 = -3 \implies x = +3 \] ### Step 2: Identify the ligand types and their coordination numbers. - **For \([CoF_6]^{3-}\)**: - Fluoride (F) is a weak field ligand and is monodentate. - The coordination number is \(6\) (since there are 6 fluoride ligands). - **For \([Co(C_2O_4)]^{3-}\)**: - The oxalate ion \((C_2O_4)^{2-}\) is a bidentate ligand. - The coordination number is also \(6\) (since it can bind through two sites). ### Step 3: Determine the hybridization based on the ligands and oxidation states. 1. **For \([CoF_6]^{3-}\)**: - Cobalt in the +3 oxidation state has the electronic configuration of \([Ar] 3d^7\). - In the presence of weak field ligands (like F), the electrons will fill the higher energy orbitals before pairing occurs. - The hybridization will be \(sp^3d^2\) because the 4s orbital is empty and the 4p orbitals are not involved in bonding. The 3d orbitals will be used for hybridization. - Therefore, the hybridization is \(sp^3d^2\). 2. **For \([Co(C_2O_4)]^{3-}\)**: - The oxalate ion is a strong field ligand, which causes pairing of electrons. - The 3d orbitals will fill first, leading to pairing before filling the higher energy orbitals. - The hybridization will be \(d^2sp^3\) because the inner d orbitals are used for hybridization. - Therefore, the hybridization is \(d^2sp^3\). ### Final Answer: - The hybridization of \([CoF_6]^{3-}\) is \(sp^3d^2\). - The hybridization of \([Co(C_2O_4)]^{3-}\) is \(d^2sp^3\).
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The hybridisation of Co in (CoF_(6))^(-2) is

The hybridization of the metal in [CoF_(6)]^(3-) is

On the basic of CET explaine the following complex of Co^(3+) like [Co(NH_(3))_(6)]^(3+),[Co(en)_(3)]^(3+) and [Co(NO_(2))_(6)]^(3-) are diamagntic while [CoF_(6)]^(3-) and [Co(H_(2)O)_(6)]^(3+) are paramagnetic .

Consider the following two complex ions : [CoF_(6)]^(3-) and [Co(C_(2)O_(4))_(3)]^(3-) . Which of the following statement(s) is/are false ? I. Both are octahedral II. [Co(C_(2)O_(4))_(3)]^(3-) is diamagnetic while [CoF_(6)]^(3-) is paramagnetic . III. Both are outer orbital complexes . IV. In both the complexes the central metal is in the same oxidation state .

The shape of [CoF_(6)]^(-3) is

Two statements 'A' and 'R' are given below Select your answers to these items using the codes given below: Assertio (A) : Among the cobalt (III) complexes [Co(NH_(3))_(6)]^(3+) is a diamagnetic but [CoF_(6)]^(3-) is paramagnetic. Reason (R) : Hybridisation of [Co(NH_(3))_(6)]^(3+) is sp^(3)d^(2) where as hybridisation of Co in [CoF_(6)]^(3-) is d^(2)sp^(3) .

Co^(3+) ion forms octahedral complex with ligands like F^(-) and NH_(3) as [CoF_(6)]^(3-) and [Co(NH_(3))_(6)]^(3+) . These two complexes differ in:

GRB PUBLICATION-COORDINATION COMPOUNDS-D.VBT, CFT, Hybridisation
  1. The species having tetrahedral shape is

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  2. Which one of the following high-spin complexes has the largest CFSE (C...

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  3. The hybridization of [CoF(6)]^(3-) and [Co(C(2)O(4))}^(3-) are :

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  4. The total crystal field stabilization energy (CFSE) for the complexes ...

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  5. Wilkinson's catalyst react with H(2) to from an octahedral complex in ...

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  6. The spin-only magnetic moment [in units of Bohr magneton, (mu(B) of Ni...

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  7. underset((X))(K(6)[(CN)(5)" "Co-O-O-Co(CN)(5)])overset("oxidizes")rarr...

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  8. The coordination number and the oxidation state of the element 'E' in ...

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  9. Which of the following is not correctly matched ?

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  10. The complex K(4)[Zn(CN)(4)(O(2))(2)] is oxidised into K(2)[Zn(CN)(4)(O...

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  11. Allthe following complexes show a decrease in their weights when place...

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  12. The geometry of [Co(CO)(4)]^(-)" and "[Cd(CN)(4)]^(2-) are :

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  13. In which option ,properties of the given three complexes are correct ?...

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  14. If triangle(0) is crystal field splitting energy and P is mean pairing...

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  15. Which of the following is inner orbital complex as well as diamagnetic...

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  16. Consider the following complexes : [NiCl(4)]^(2-), [Ni(CN)(4)]^(2-),...

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  17. [Ni(CN)(4)]^(2-)" and "[NiCl(4)]^(2-) have similarity but not in :

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  18. For which of the following d^(n) configuration of octahedral complex(e...

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  19. The correct order of energies of d-orbitals of metal ion in a square p...

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  20. According to crystal field theory (CFT) :

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