Animated Solution for Chemistry - Coordination Compounds: The sum of the spin only magnetic moment values (in B.M.) of [Mn(Br)6]3− and [Mn(CN)6]3− is ______.
Enter Numerical Value:
Visualized Solution
OxidationStateofManganese
Let the oxidation state of Mn be x.
For [Mn(Br)6]3−: x+6(−1)=−3⟹x=+3
For [Mn(CN)6]3−: x+6(−1)=−3⟹x=+3
ElectronicConfiguration
Mn (Z=25):[Ar]3d54s2
Mn3+:[Ar]3d4
Magnetic moment formula: μ=n(n+2) B.M.
CrystalFieldSplittingin[Mn(Br)6]3−
Br− is a weak field ligand (WFL).
Δo<P (Splitting energy is less than pairing energy).
Electrons will not pair up easily; it forms a high-spin complex.
MagneticMomentof[Mn(Br)6]3−
Configuration: t2g3eg1
Number of unpaired electrons, n=4
μ1=4(4+2)=24≈4.90 B.M.
CrystalFieldSplittingin[Mn(CN)6]3−
CN− is a strong field ligand (SFL).
Δo>P (Splitting energy is greater than pairing energy).
Electrons will pair up; it forms a low-spin complex.
MagneticMomentof[Mn(CN)6]3−
Configuration: t2g4eg0
Number of unpaired electrons, n=2
μ2=2(2+2)=8≈2.83 B.M.
TotalMagneticMoment
Sum=μ1+μ2
Sum=4.90+2.83=7.73 B.M.
TheWayForward
Magnetic moment measurements are crucial for experimentally determining whether a complex is high-spin or low-spin.
This reveals the strength of the ligand field and the geometry of the complex.
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The Sigma Insight: Bonding and Crystal field
Solution Diagram
Decoding the Oxidation State
To solve this problem, we first need to understand the state of our central metal ion, Manganese (Mn), in both complexes: [Mn(Br)6]3− and [Mn(CN)6]3−.
Both bromide (Br−) and cyanide (CN−) are monoanionic ligands, meaning they carry a charge of −1. Since there are six ligands in each complex and the overall charge of the coordination sphere is −3, we can set up a simple algebraic equation to find the oxidation state of Manganese (x):
x+6(−1)=−3
Solving this gives x=+3. Thus, Manganese is in the +3 oxidation state in both complexes.
The Electronic Configuration
Manganese has an atomic number of 25. Its neutral ground-state electronic configuration is [Ar]3d54s2. When it loses three electrons to form the Mn3+ ion, it loses the two 4s electrons first, followed by one 3d electron. This leaves us with a 3d4 configuration.
Now, we have four d-electrons to place in the split d-orbitals. How they are placed depends entirely on the nature of the approaching ligands.
The Battle of the Ligands
Weak vs. Strong
According to Crystal Field Theory (CFT), the five degenerate d-orbitals split into two distinct energy levels in an octahedral field: the lower energy t2g level and the higher energy eg level. The energy gap between them is denoted by Δo.
For [Mn(Br)6]3−:
Bromide is a weak field ligand. It causes a very small splitting, meaning Δo is less than the pairing energy (P). Because the gap is small, the fourth electron finds it easier to jump up to the eg level rather than pairing up in the t2g level. This results in a high-spin complex with the configuration t2g3eg1. We have exactly n=4 unpaired electrons.
Using the spin-only magnetic moment formula:
μ=n(n+2)
μ1=4(4+2)=24≈4.90 B.M.
For [Mn(CN)6]3−:
Cyanide, on the other hand, is a strong field ligand. It causes a massive splitting, making Δo much greater than the pairing energy (P). The energy gap is too large to cross, so the fourth electron is forced to pair up in the lower t2g level. This results in a low-spin complex with the configuration t2g4eg0. Here, we have one pair and n=2 unpaired electrons.
Applying the formula again:
μ2=2(2+2)=8≈2.83 B.M.
The Final Summation
The question asks for the sum of these two magnetic moment values.
Sum=μ1+μ2
Sum=4.90+2.83=7.73 B.M.
This beautiful problem perfectly illustrates how different ligands can drastically alter the quantum mechanical properties of a molecule, changing its magnetic behavior entirely!