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Corystal field splitting energy (CFSE) f...

Corystal field splitting energy `(CFSE)` for the complex `[Cr(H_(2)O)_(6)]^(2+)` is when `(DeltaltP)` .

A

` 1.2Delat_(0)`

B

`-0.6Delta_(0)`

C

`0.6Delta_(0)`

D

`1.2Delta_(0)`

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The correct Answer is:
To solve the problem of calculating the Crystal Field Splitting Energy (CFSE) for the complex \([Cr(H_2O)_6]^{2+}\), we will follow these steps: ### Step 1: Determine the Oxidation State of Chromium The complex is \([Cr(H_2O)_6]^{2+}\). Since water (H2O) is a neutral ligand, the oxidation state of chromium can be calculated as follows: Let the oxidation state of chromium be \(x\). \[ x + 6(0) = +2 \implies x = +2 \] Thus, the oxidation state of chromium in this complex is +2. **Hint:** Always start by determining the oxidation state of the metal in the coordination complex. ### Step 2: Write the Electron Configuration of Chromium The atomic number of chromium (Cr) is 24. The ground state electron configuration is: \[ \text{Cr: } [Ar] 4s^1 3d^5 \] For the +2 oxidation state, two electrons are removed (first from the 4s and then from the 3d): \[ \text{Cr}^{2+}: [Ar] 3d^4 \] **Hint:** Remember that when determining the electron configuration for cations, electrons are removed from the outermost shell first. ### Step 3: Distribute Electrons in the Crystal Field In an octahedral field, the \(d\) orbitals split into two sets: \(t_{2g}\) (lower energy) and \(e_g\) (higher energy). For \(d^4\) configuration: - The first three electrons will fill the \(t_{2g}\) orbitals. - The fourth electron will go into the \(e_g\) orbital because the splitting energy (\(\Delta\)) is less than the pairing energy. The distribution will be: - \(t_{2g} = 3\) electrons - \(e_g = 1\) electron **Hint:** In an octahedral field, fill the lower energy orbitals first before moving to higher energy orbitals, especially when the splitting energy is low. ### Step 4: Calculate the CFSE The formula for CFSE is given by: \[ \text{CFSE} = (0.4 \times \text{number of electrons in } t_{2g}) - (0.6 \times \text{number of electrons in } e_g) \] Substituting the values: \[ \text{CFSE} = (0.4 \times 3) - (0.6 \times 1) = 1.2 - 0.6 = 0.6 \] Since CFSE is typically expressed as a negative value (indicating stabilization), we write: \[ \text{CFSE} = -0.6 \] **Hint:** Remember the coefficients for \(t_{2g}\) and \(e_g\) when calculating CFSE; they reflect the energy associated with electron placement in these orbitals. ### Conclusion The Crystal Field Splitting Energy (CFSE) for the complex \([Cr(H_2O)_6]^{2+}\) is \(-0.6\). **Final Answer:** \(-0.6\)

To solve the problem of calculating the Crystal Field Splitting Energy (CFSE) for the complex \([Cr(H_2O)_6]^{2+}\), we will follow these steps: ### Step 1: Determine the Oxidation State of Chromium The complex is \([Cr(H_2O)_6]^{2+}\). Since water (H2O) is a neutral ligand, the oxidation state of chromium can be calculated as follows: Let the oxidation state of chromium be \(x\). \[ x + 6(0) = +2 \implies x = +2 ...
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