The sum of the spin-only magnetic moment values (in B.M.) of $[\text{Mn}(\text{Br})_6]^{3-}$ and $[\text{Mn}(\text{CN})_6]^{3-}$ is ____.
Both complexes, [Mn(Br)6]³⁻ and [Mn(CN)6]³⁻, have an overall charge of -3. The ligands Br⁻ and CN⁻ are monodentate anions, each with a charge of -1. Let’s calculate the oxidation state of Mn.
For [Mn(Br)6]³⁻:
\[ x + 6(-1) = -3 \implies x - 6 = -3 \implies x = +3 \]
For [Mn(CN)6]³⁻:
\[ x + 6(-1) = -3 \implies x = +3 \]
Thus, Mn has an oxidation state of +3 in both complexes, a key concept for JEE Advanced coordination chemistry.
The atomic number of Mn is 25, with an electronic configuration of:
\[ [Ar]\,3d^5\,4s^2 \]
For Mn³⁺, remove 2 electrons from 4s and 1 from 3d:
\[ [Ar]\,3d^4 \]
This d4 configuration is critical for determining the spin state and magnetic properties, a common topic in JEE Advanced inorganic chemistry.
The nature of ligands determines whether the complex is high spin or low spin, a key concept in coordination compounds for JEE Advanced:
This distinction affects the electron arrangement and magnetic moment.
The spin-only magnetic moment (\(\mu_s\)) is calculated using:
\[ \mu_s = \sqrt{n(n+2)} \quad \text{B.M.} \]
Where \( n \) is the number of unpaired electrons.
For [Mn(Br)6]³⁻ (high spin, d⁴):
Electron arrangement in octahedral field: \( t_{2g}^3 e_g^1 \)
This gives 4 unpaired electrons:
\[ \mu_s = \sqrt{4(4+2)} = \sqrt{24} = 4.90 \approx 5 \, \text{B.M.} \]
For [Mn(CN)6]³⁻ (low spin, d⁴):
Electron arrangement: \( t_{2g}^4 e_g^0 \)
This gives 2 unpaired electrons:
\[ \mu_s = \sqrt{2(2+2)} = \sqrt{8} = 2.83 \approx 2.8 \, \text{B.M.} \]
These calculations align with JEE Advanced expectations for magnetic moment problems.
Add the magnetic moments of both complexes:
\[ 5 + 2.8 = 7.8 \approx 7 \]
Final Answer: The sum of the spin-only magnetic moments is approximately 7 B.M.