Which is more likely to be paramagnetic, \(\mathrm{Fe}(\mathrm{CN})_{6}^{4-}\) or \(\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}^{2+} ?\) Explain.

Short Answer

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The \(\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}^{2+}\) complex is more likely to be paramagnetic, as it has four unpaired electrons in its 3d orbitals, while \(\mathrm{Fe}(\mathrm{CN})_{6}^{4-}\) has only one unpaired electron in the 4s orbital. This is due to the weak-field ligand (H2O) bonding in the \(\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}^{2+}\) complex not resulting in the pairing of electrons in its d-orbitals, while strong-field ligand (CN-) bonding in the \(\mathrm{Fe}(\mathrm{CN})_{6}^{4-}\) complex does.

Step by step solution

01

Finding the oxidation state of iron in each complex

Let's find the oxidation state of iron (Fe) in each complex. In the complex \(\mathrm{Fe}(\mathrm{CN})_{6}^{4-}\): Each CN ligand has a charge of -1, so the overall charge due to the 6 CN ligands is -6. Since the net charge of the complex is -4, the charge on iron must be: \[+2\ (\text{for balancing the overall charge})\] In the complex \(\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}^{2+}\): Each H2O ligand has a charge of 0. Since the net charge of the complex is +2, the charge on iron must be: \[+2\ (\text{as given by the complex})\]
02

Analyzing the electron configurations of iron in each complex

Now, let's analyze the electron configurations of iron. In both complexes, the oxidation state of iron is +2, which means it has lost 2 electrons from its neutral state of Fe (\(\text{atomic number}=26\)). The electron configuration of neutral iron is: \[[\text{Ar}] 3d^6 4s^2\] After losing 2 electrons, the electron configuration of Fe(II) will be: \[[\text{Ar}] 3d^6\]
03

Determine unpaired electrons in the d-orbitals

Now we need to determine the number of unpaired electrons in the d-orbitals of both complexes. For \(\mathrm{Fe}(\mathrm{CN})_{6}^{4-}\): The Fe(II) ion in this complex undergoes strong-field ligand (CN-) bonding, which results in the pairing of electrons in its d-orbitals. Its electron configuration becomes: \[[\text{Ar}] 3d^5 4s^1\] (Note that there is only one unpaired electron in the 4s orbital) For \(\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}^{2+}\): The Fe(II) ion in this complex undergoes weak-field ligand (H2O) bonding, which does not result in the pairing of electrons in its d-orbitals. Its electron configuration remains: \[[\text{Ar}] 3d^6\] (Note that there are four unpaired electrons in the 3d orbitals)
04

Comparing the unpaired electrons in both complexes

We have determined the number of unpaired electrons in both complexes: - In \(\mathrm{Fe}(\mathrm{CN})_{6}^{4-}\), there is only one unpaired electron in the 4s orbital. - In \(\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}^{2+}\), there are four unpaired electrons in the 3d orbitals. Since the \(\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}^{2+}\) complex has more unpaired electrons, it is more likely to be paramagnetic.

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Most popular questions from this chapter

In which of the following is(are) the electron configuration(s) correct for the species indicated? a. Cu \([\mathrm{Ar}] 4 s^{2} 3 d^{9}\) b. \(\mathrm{Fe}^{3+} \quad[\mathrm{Ar}] 3 d^{5}\) c. Co \([\mathrm{Ar}] 4 s^{2} 3 d^{7}\) d. La \([\mathrm{Ar}] 6 s^{2} 4 f^{1}\) e. \(\mathrm{Pt}^{2+} \quad[\mathrm{Xe}] 4 f^{14} 5 d^{8}\)

Qualitatively draw the crystal field splitting of the \(d\) orbitals in a trigonal planar complex ion. (Let the \(z\) axis be perpendicular to the plane of the complex.)

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