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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. Select the correct statement regarding `[Cr(en)_(2)Cl_(2)]^(+) and [Co(C_(2)O_(4))_(2)(NH_(3))_(2)]^(-)` complex ions:

A

Both are equally stable complexes

B

Both have equal number of stereoisomers

C

Both are diamagnetic complexes

D

a and c both

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To solve the question regarding the complex ions \([Cr(en)_2Cl_2]^+\) and \([Co(C_2O_4)_2(NH_3)_2]^-\), we need to analyze the oxidation states, electronic configurations, and the nature of the ligands involved. ### Step-by-Step Solution: 1. **Determine the Oxidation State of Chromium in \([Cr(en)_2Cl_2]^+\)**: - Ethylene diamine (en) is a neutral ligand, contributing 0 to the charge. - Each chloride ion (Cl) has a charge of -1. Since there are 2 Cl ligands, they contribute -2 to the charge. - Let the oxidation state of chromium be \(x\). The overall charge of the complex is +1. - Therefore, the equation is: \[ x + 0 + (-2) = +1 \implies x - 2 = 1 \implies x = +3 \] - Thus, the oxidation state of chromium is +3. 2. **Determine the Electronic Configuration of Chromium**: - The atomic number of chromium (Cr) is 24. The ground state electronic configuration is \([Ar] 3d^5 4s^1\). - For \(Cr^{3+}\), we remove 3 electrons (2 from 4s and 1 from 3d): \[ 3d^3 \] 3. **Determine the Oxidation State of Cobalt in \([Co(C_2O_4)_2(NH_3)_2]^-\)**: - Oxalate ion \((C_2O_4)^{2-}\) is a bidentate ligand with a charge of -2. Since there are 2 oxalate ligands, they contribute -4 to the charge. - Ammonia (NH3) is a neutral ligand, contributing 0 to the charge. - Let the oxidation state of cobalt be \(y\). The overall charge of the complex is -1. - Therefore, the equation is: \[ y + (-4) + 0 = -1 \implies y - 4 = -1 \implies y = +3 \] - Thus, the oxidation state of cobalt is +3. 4. **Determine the Electronic Configuration of Cobalt**: - The atomic number of cobalt (Co) is 27. The ground state electronic configuration is \([Ar] 3d^7 4s^2\). - For \(Co^{3+}\), we remove 3 electrons (2 from 4s and 1 from 3d): \[ 3d^6 \] 5. **Analyze the Ligands**: - Ethylene diamine (en) is a strong field ligand, which causes a large splitting of the d-orbitals. - Oxalate ion (C2O4) is also a strong field ligand, but ammonia (NH3) is a moderate field ligand. - Therefore, in \([Cr(en)_2Cl_2]^+\), the strong field ligand (en) will lead to a higher splitting energy (\(\Delta_o\)), while in \([Co(C_2O_4)_2(NH_3)_2]^-\), the combination of oxalate and ammonia will also lead to significant splitting. 6. **Determine Magnetic Properties**: - \(Cr^{3+}\) with \(3d^3\) has unpaired electrons, making it paramagnetic. - \(Co^{3+}\) with \(3d^6\) can be diamagnetic if all electrons are paired, which is likely in the presence of strong field ligands. 7. **Conclusion**: - The correct statement regarding these complex ions is that they have different magnetic properties due to the different numbers of unpaired electrons.
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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. Which of the following is correct statement?

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+)

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+)

Give the number of unpaired electrons in t_(2g) set of d-orbitals in [Co(H_(2)O)_(3)F_(3)] complex .

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:

The reaction 3O_(2)(g) rarr 2O_(3)(g), Delta_(r )H > 0 . What can be concluded about average energy per bond in O_(2) and O_(3) ?

Assertion : According to crystal field theory , during complex formation , the d-orbitals split and form two sets of orbitals t_(2g) and e_(g) . Reason : Splitting of d-orbitals occurs only in case of strong field ligands .

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. Cr^(3+) form four complexes with four different ligands which are [Cr(Cl)_(6)]^(3-), [Cr(H_(2)O)_(6)]^(3+) , [Cr(NH_(3))_(6)]^(3+) and [Cr(CN)_(6)]^(3-) , the order of CFSE (Delta_(0)) in these complexes in the order:

At constant T and P ,Which of the following statements is correct for the reaction, CO(G)+(1)/(2)O_(2)(g)rarrCO_(2)(g) ,

Predict DeltaH gt DeltaU or DeltaH lt DeltaU . a. C("graphite") +O_(2)(g) rarr CO_(2)(g) b. PCl_(5)(g) rarr PCl_(3)(g) +Cl_(2)(g)

VK JAISWAL ENGLISH-CO-ORDINATION COMPOUNDS-LEVEL 3 (PASSAGE TYPE)
  1. In complexes off wea field ligands, Delta(o) lt P (pairing energy), th...

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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