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[Fe(H(2)O)(6)]^(3+) and [Fe(CN)(6)]^(3-)...

`[Fe(H_(2)O)_(6)]^(3+) and [Fe(CN)_(6)]^(3-)` differ in

A

Oxidation number

B

Coordination number

C

Structure

D

Magnetic nature

Text Solution

AI Generated Solution

The correct Answer is:
To determine how the complexes \([Fe(H_2O)_6]^{3+}\) and \([Fe(CN)_6]^{3-}\) differ, we will analyze their oxidation states, coordination numbers, structures, and magnetic properties step by step. ### Step 1: Determine the Oxidation State 1. For \([Fe(H_2O)_6]^{3+}\): - Let the oxidation state of Fe be \(X\). - Water (\(H_2O\)) is a neutral ligand, contributing 0 to the charge. - The overall charge of the complex is \(+3\). - Therefore, we have the equation: \[ X + 0 = +3 \implies X = +3 \] 2. For \([Fe(CN)_6]^{3-}\): - Let the oxidation state of Fe be \(Y\). - Each cyanide (\(CN^-\)) has a charge of \(-1\). - The overall charge of the complex is \(-3\). - Therefore, we have the equation: \[ Y + 6(-1) = -3 \implies Y - 6 = -3 \implies Y = +3 \] **Conclusion**: The oxidation state of Fe in both complexes is \(+3\). ### Step 2: Determine the Coordination Number 1. For \([Fe(H_2O)_6]^{3+}\): - There are 6 water molecules coordinated to Fe. - Therefore, the coordination number is \(6\). 2. For \([Fe(CN)_6]^{3-}\): - There are 6 cyanide ligands coordinated to Fe. - Therefore, the coordination number is also \(6\). **Conclusion**: The coordination number for both complexes is \(6\). ### Step 3: Determine the Structure - Both complexes have octahedral geometry due to the coordination number of \(6\). **Conclusion**: Both complexes have the same octahedral structure. ### Step 4: Determine the Magnetic Nature 1. For \([Fe(H_2O)_6]^{3+}\): - The electronic configuration of \(Fe^{3+}\) is \(3d^5\). - Water is a weak field ligand, which does not cause pairing of electrons. - Therefore, all five \(3d\) electrons remain unpaired. - The number of unpaired electrons (\(n\)) is \(5\). - The magnetic moment (\(\mu\)) can be calculated using: \[ \mu = \sqrt{n(n + 2)} = \sqrt{5(5 + 2)} = \sqrt{35} \approx 5.916 \text{ Bohr magneton} \] 2. For \([Fe(CN)_6]^{3-}\): - The electronic configuration of \(Fe^{3+}\) is still \(3d^5\). - Cyanide is a strong field ligand, which causes pairing of electrons. - Therefore, there is only \(1\) unpaired electron. - The number of unpaired electrons (\(n\)) is \(1\). - The magnetic moment (\(\mu\)) can be calculated using: \[ \mu = \sqrt{n(n + 2)} = \sqrt{1(1 + 2)} = \sqrt{3} \approx 1.732 \text{ Bohr magneton} \] **Conclusion**: - \([Fe(H_2O)_6]^{3+}\) is strongly paramagnetic with a magnetic moment of approximately \(5.916\) Bohr magneton. - \([Fe(CN)_6]^{3-}\) is weakly paramagnetic with a magnetic moment of approximately \(1.732\) Bohr magneton. ### Final Conclusion The two complexes differ in their magnetic nature. Therefore, the correct answer is that they differ in **magnetic nature**. ---
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