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In complexes off wea field ligands, Delt...

In complexes off wea field ligands, `Delta_(o) lt P` (pairing energy), the energy difference between `t_(2g) and e_(g)` sets is relatively less. Under the unfluence of strong field ligands, `Delta_(O) gt p` (Pairing energy), the energy difference between `t_(2g) and e_(g)` sets is relatively high.
Q. Which of the following is correct statement?

A

Complex `[Co(H_(2)O)_(6)]^(2+)` is more stable than `[Co(H_(2)O)_(6)]^(3+)`

B

All compounds of `Ni(II)` are bound to be outer-d-orbital complexes

C

Stability constant for `[Ni(en)_(3)]^(2+)` is greater than stability constant for `[Ni(NH_(3))_(6)]^(2+)`

D

`Delta_(oct)` for `[Cr(H_(2)O)_(6)]^(3+)` is greater than `Delta_(oct)` for `[Cr(NH_(3))_(6)]^(3+)`

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The correct Answer is:
To solve the question regarding the stability of complexes with weak and strong field ligands, we will analyze the provided statements step by step. ### Step-by-Step Solution: 1. **Understanding Ligands and Splitting Energy**: - Weak field ligands cause a smaller splitting of the d-orbitals, which means that the energy difference between the \( t_{2g} \) and \( e_g \) sets is relatively small. This results in less energy required for pairing of electrons. - Strong field ligands, on the other hand, cause a larger splitting of the d-orbitals, leading to a higher energy difference between \( t_{2g} \) and \( e_g \) sets. This means that the energy required for pairing electrons is greater. 2. **Analyzing the Statements**: - **Statement 1**: "The stability of \( [Co(H_2O)_6]^{2+} \) is more than \( [Co(H_2O)_6]^{3+} \)". - This statement is incorrect. The \( [Co(H_2O)_6]^{3+} \) complex has a higher oxidation state, which generally increases stability due to increased positive charge attracting the ligands more strongly. - **Statement 2**: "All compounds of \( Ni^{2+} \) are bound to be outer d orbital complexes". - This statement is also incorrect. While \( Ni^{2+} \) typically has a configuration of \( 3d^8 \), it can form inner d orbital complexes in the presence of strong field ligands, leading to pairing of electrons. - **Statement 3**: "The stability constant for \( [Ni(en)_3]^{2+} \) is greater than that of \( [Ni(NH_3)_6]^{2+} \)". - This statement is correct. Ethylenediamine (en) is a stronger field ligand compared to ammonia (NH₃), leading to a higher stability constant for the \( [Ni(en)_3]^{2+} \) complex. - **Statement 4**: "The octahedral complex \( [Cr(H_2O)_6]^{3+} \) is more stable than the given complex". - This statement is incorrect. \( [Cr(H_2O)_6]^{3+} \) involves weak field ligands, and if compared with a strong field ligand complex, it would generally be less stable. 3. **Conclusion**: - Based on the analysis, the only true statement is Statement 3. Therefore, the correct answer to the question is: - **Option C**: "The stability constant for \( [Ni(en)_3]^{2+} \) is greater than that of \( [Ni(NH_3)_6]^{2+} \)".
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In complexes off wea field ligands, Delta_(o) lt P (pairing energy), the energy difference between t_(2g) and e_(g) sets is relatively less. Under the unfluence of strong field ligands, Delta_(O) gt p (Pairing energy), the energy difference between t_(2g) and e_(g) sets is relatively high. Q. Select the correct statement regarding [Cr(en)_(2)Cl_(2)]^(+) and [Co(C_(2)O_(4))_(2)(NH_(3))_(2)]^(-) complex ions:

In complexes off wea field ligands, Delta_(o) lt P (pairing energy), the energy difference between t_(2g) and e_(g) sets is relatively less. Under the unfluence of strong field ligands, Delta_(O) gt p (Pairing energy), the energy difference between t_(2g) and e_(g) sets is relatively high. Q. Select the correct increasing order of 10 Dq. value of chromium complexes: (1) [Cr(en)_(3)]^(3+) (2) [Cr(o x)_(3)]^(3-) (3) [CrF_(6)]^(3-) (4) [Cr(H_(2)O)_(6)]^(3+)

In complexes off wea field ligands, Delta_(o) lt P (pairing energy), the energy difference between t_(2g) and e_(g) sets is relatively less. Under the unfluence of strong field ligands, Delta_(O) gt p (Pairing energy), the energy difference between t_(2g) and e_(g) sets is relatively high. Q. Select the correct increasing order of 10 Dq. value of chromium complexes: (1) [Cr(en)_(3)]^(3+) (2) [Cr(o x)_(3)]^(3-) ltBrgt (3) [CrF_(6)]^(3-) (4) [Cr(H_(2)O)_(6)]^(3+)

The activation energies of two reactions are E_(a1) and E_(a2) with E_(a1) gt E_(a2) . If the temperature of the reacting systems is increased from T to T' , which of the following is correct?

The activation energies of two reactions are E_(a1) and E_(a2) with E_(a1) gt E_(a2) . If the temperature of the reacting systems is increased from T to T' , which of the following is correct?

Consider following reaction: Cl_(2)(g)+H_(2)O overset(R.T.)to P+Q If molecular weight of P is less than Q then incorrect statement is:

When degenerate d-orbitals of an isolated atom/ion come under influence of magnetic field of ligands, the degeneray is lost. The two set t_(2g)(d_(xy),d_(yz),d_(xz)) and e_(g) (d_(x^(2))-d_(x^(2)-y^(2)) are either stabilized or destabilized depending upon the nature of magnetic field. it can be expressed diagrammatically as: 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 complex). this energy lies in visible region and i.e., why electronic transition are responsible for colour. such transition are not possible with d^(0) and d^(10) configuration. Q. Which of the following is correct arrangement of ligand in terms of the Dq values of their complexes with any particularr 'hard' metal ion:

When degenerate d-orbitals of an isolated atom/ion come under influence of magnetic field of ligands, the degeneray is lost. The two set t_(2g)(d_(xy),d_(yz),d_(xz)) and e_(g) (d_(x^(2))-d_(x^(2)-y^(2)) are either stabilized or destabilized depending upon the nature of magnetic field. it can be expressed diagrammatically as: 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 complex). this energy lies in visible region and i.e., why electronic transition are responsible for colour. such transition are not possible with d^(0) and d^(10) configuration. Q. Which of the following is correct arrangement of ligand in terms of the Dq values of their complexes with any particularr 'hard' metal ion:

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VK JAISWAL ENGLISH-CO-ORDINATION COMPOUNDS-LEVEL 3 (PASSAGE TYPE)
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  2. An isomer of the complex Co(en)(2)(H(2)O)IC l(2), on reaction with con...

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  3. In complexes off wea field ligands, Delta(o) lt P (pairing energy), th...

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  4. In complexes off wea field ligands, Delta(o) lt P (pairing energy), th...

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  5. In complexes off wea field ligands, Delta(o) lt P (pairing energy), th...

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  6. Complex compounds are molecular compounds which retain their identitie...

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  7. Complex compounds are molecular compounds which retain their identitie...

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  8. Complex compounds are molecular compounds which retain their identitie...

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  9. Recent X-ray work, IR and other spectroscopic methods have proved that...

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  10. Recent X-ray work, IR and other spectroscopic methods have proved that...

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  11. On the basic of stability of complex ion in the solution, complexes ma...

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  12. On the basic of stability of complex ion in the solution, complexes ma...

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  13. When degenerate d-orbitals of an isolated atom/ion come under influenc...

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  14. When degenerate d-orbitals of an isolated atom/ion come under influenc...

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  15. When degenerate d-orbitals of an isolated atom/ion come under influenc...

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  16. When degenerate d-orbitals of an isolated atom/ion come under influenc...

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  17. When degenerate d-orbitals of an isolated atom/ion come under influenc...

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  18. When degenerate d-orbitals of an isolated atom/ion come under influenc...

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  19. When degenerate d-orbitals of an isolated atom/ion come under influenc...

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  20. Magnetic moment, ionic conductance and colligative properties are usef...

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