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Given following complexes (I) Na4[Fe(C...

Given following complexes
`(I) Na_4[Fe(CN)_6] (II) [Cr(H_2O)_6] Cl_2 (III) (NEt_4)_2 [CoCl_4] (IV) Na_3[Fe(C_2O_4)_3] (Delta_0 gt P)`
Correct order of spin only magnetic moment for the above complexes is

A

`(II) gt (III) gt (IV) gt I`

B

`(II) gt (IV) gt (III) gt (I)`

C

`(I) gt (IV) gt (III) gt (II)`

D

`(II) gt (I) gt (IV) gt (III)`

Text Solution

AI Generated Solution

The correct Answer is:
To determine the correct order of spin-only magnetic moments for the given complexes, we will analyze each complex step by step, find the oxidation states, electronic configurations, and then calculate the magnetic moments. ### Step 1: Analyze Complex (I) Na₄[Fe(CN)₆] 1. **Determine the oxidation state of Iron (Fe)**: - Sodium (Na) has a +1 charge, so 4 Na contributes +4. - The complex ion [Fe(CN)₆] has an overall charge of -4. - Let the oxidation state of Fe be \( x \): \[ x + 6(-1) = -4 \implies x - 6 = -4 \implies x = +2 \] 2. **Electronic configuration of Fe²⁺**: - Fe (atomic number 26) has the configuration [Ar] 3d⁶ 4s². - For Fe²⁺, it loses two electrons (from 4s), resulting in 3d⁶. 3. **Determine the geometry and field strength**: - CN⁻ is a strong field ligand, leading to pairing of electrons. - The electron filling in the d-orbitals will be: \[ \text{t}_{2g}^6 \text{e}_g^0 \] - **Number of unpaired electrons**: 0. 4. **Calculate magnetic moment**: \[ \mu = \sqrt{n(n+2)} = \sqrt{0(0+2)} = 0 \] ### Step 2: Analyze Complex (II) [Cr(H₂O)₆]Cl₂ 1. **Determine the oxidation state of Chromium (Cr)**: - Water (H₂O) is neutral, and Cl⁻ has a -1 charge. - Let the oxidation state of Cr be \( x \): \[ x + 6(0) + 2(-1) = 0 \implies x - 2 = 0 \implies x = +2 \] 2. **Electronic configuration of Cr²⁺**: - Cr (atomic number 24) has the configuration [Ar] 3d⁵ 4s¹. - For Cr²⁺, it loses one 4s and one 3d electron, resulting in 3d⁴. 3. **Determine the geometry and field strength**: - H₂O is a weak field ligand, leading to no pairing. - The electron filling in the d-orbitals will be: \[ \text{t}_{2g}^3 \text{e}_g^1 \] - **Number of unpaired electrons**: 4. 4. **Calculate magnetic moment**: \[ \mu = \sqrt{n(n+2)} = \sqrt{4(4+2)} = \sqrt{24} \approx 4.9 \, \mu_B \] ### Step 3: Analyze Complex (III) (NEt₄)₂[CoCl₄] 1. **Determine the oxidation state of Cobalt (Co)**: - The complex ion [CoCl₄] has a -2 charge. - Let the oxidation state of Co be \( x \): \[ x + 4(-1) = -2 \implies x - 4 = -2 \implies x = +2 \] 2. **Electronic configuration of Co²⁺**: - Co (atomic number 27) has the configuration [Ar] 3d⁷ 4s². - For Co²⁺, it loses two electrons (from 4s), resulting in 3d⁷. 3. **Determine the geometry and field strength**: - Cl⁻ is a weak field ligand, leading to no pairing. - The electron filling in the d-orbitals will be: \[ \text{t}_{2g}^5 \text{e}_g^2 \] - **Number of unpaired electrons**: 3. 4. **Calculate magnetic moment**: \[ \mu = \sqrt{n(n+2)} = \sqrt{3(3+2)} = \sqrt{15} \approx 3.87 \, \mu_B \] ### Step 4: Analyze Complex (IV) Na₃[Fe(C₂O₄)₃] 1. **Determine the oxidation state of Iron (Fe)**: - Oxalate (C₂O₄) has a -2 charge and there are 3 oxalate ligands. - Let the oxidation state of Fe be \( x \): \[ x + 3(-2) = -3 \implies x - 6 = -3 \implies x = +3 \] 2. **Electronic configuration of Fe³⁺**: - For Fe³⁺, it loses three electrons (from 4s and 3d), resulting in 3d⁵. 3. **Determine the geometry and field strength**: - Oxalate is a bidentate ligand and a strong field ligand (given that \( \Delta_0 > P \)). - The electron filling in the d-orbitals will be: \[ \text{t}_{2g}^5 \text{e}_g^0 \] - **Number of unpaired electrons**: 1. 4. **Calculate magnetic moment**: \[ \mu = \sqrt{n(n+2)} = \sqrt{1(1+2)} = \sqrt{3} \approx 1.73 \, \mu_B \] ### Summary of Magnetic Moments - Complex (I): \( \mu = 0 \) - Complex (II): \( \mu \approx 4.9 \) - Complex (III): \( \mu \approx 3.87 \) - Complex (IV): \( \mu \approx 1.73 \) ### Correct Order of Spin-Only Magnetic Moments From the calculated values: 1. Complex (II) > Complex (III) > Complex (IV) > Complex (I) Thus, the correct order of spin-only magnetic moments is: **(II) > (III) > (IV) > (I)**
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