Why do transition metals have more oxidation states than other elements? Give the highest oxidation states for scandium to copper.

Short Answer

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Transition metals have more oxidation states as they have electrons in both s and d orbitals which can be lost to form cations. The highest oxidation states for the transition metals from scandium to copper are +3 for Sc and Fe, +4 for Ti, +5 for V, +6 for Cr, +7 for Mn, +3 for Co, +2 for Ni and Cu.

Step by step solution

01

Understanding the Electronic Configuration of Transition Metals

Transition metals have electrons in their d orbitals, in addition to their outermost s orbitals. Because both the \(4s\) and \(3d\) orbitals are close in energy, electrons can be removed from either when forming ions, leading to multiple oxidation states. For example, losing one electron, typically from the \(4s\) orbital first, creates a +1 oxidation state. Further loss of electrons from the \(3d\) orbitals gives higher oxidation states.
02

Determining the Oxidation States of Scandium to Copper

Scandium (Sc) has the electronic configuration \([Ar] 3d^1 4s^2\), and can form Sc^3+ by losing all three of its valence electrons, so its highest oxidation state is +3. Titanium (Ti) has the configuration \([Ar] 3d^2 4s^2\), and can form Ti^4+ by losing all four valence electrons, so its highest oxidation state is +4. Vanadium (V) has \([Ar] 3d^3 4s^2\), and can form V^5+ by losing all five valence electrons, giving it a highest oxidation state of +5. Chromium (Cr) has \([Ar] 3d^5 4s^1\), and can lose all six valence electrons to form Cr^6+, so its highest oxidation state is +6. Manganese (Mn) has \([Ar] 3d^5 4s^2\), and can form Mn^7+ by losing all seven valence electrons, so its highest oxidation state is +7. From iron (Fe) to copper (Cu), the number of valence electrons decreases again, so iron can form Fe^3+, cobalt (Co) also can form Co^3+, nickel (Ni) can form Ni^2+, and copper can form Cu^2+ so their highest oxidation states are +3, +3, +2, +2 respectively.

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Most popular questions from this chapter

Copper is also known to exist in +3 oxidation state, which is believed to be involved in some biological electron transfer reactions. (a) Would you expect this oxidation state of copper to be stable? Explain. (b) Name the compound \(\mathrm{K}_{3} \mathrm{CuF}_{6}\) and predict the geometry of the complex ion and its magnetic properties. (c) Most of the known Cu(III) compounds have square planar geometry. Are these compounds diamagnetic or paramagnetic?

The \(\left[\mathrm{Ni}(\mathrm{CN})_{4}\right]^{2-}\) ion, which has a square planar geometry, is diamagnetic, whereas the \(\left[\mathrm{NiCl}_{4}\right]^{2-}\) ion, which has a tetrahedral geometry, is paramagnetic. Show the crystal field splitting diagrams for those two complexes.

The absorption maximum for the complex ion \(\left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{6}\right]^{3+}\) occurs at \(470 \mathrm{nm}\). (a) Predict the color of the complex and (b) calculate the crystal field splitting in kilojoules per mole.

\(\left[\mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{2} \mathrm{Cl}_{2}\right]\) is found to exist in two geometric isomers designated I and II, which react with oxalic acid as follows: $$\begin{aligned}\mathrm{I}+\mathrm{H}_{2} \mathrm{C}_{2} \mathrm{O}_{4} & \longrightarrow\left[\mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{2} \mathrm{C}_{2} \mathrm{O}_{4}\right] \\\\\mathrm{II}+\mathrm{H}_{2} \mathrm{C}_{2} \mathrm{O}_{4} & \longrightarrow\left[\mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{2}\left(\mathrm{HC}_{2} \mathrm{O}_{4}\right)_{2}\right]\end{aligned}$$ Comment on the structures of I and II.

In a dilute nitric acid solution, \(\mathrm{Fe}^{3+}\) reacts with thiocyanate ion \(\left(\mathrm{SCN}^{-}\right)\) to form a dark-red complex: $$\left[\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{3+}+\mathrm{SCN}^{-} \rightleftharpoons \mathrm{H}_{2} \mathrm{O}+\left[\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{5} \mathrm{NCS}\right]^{2+}$$ The equilibrium concentration of \(\left[\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{5} \mathrm{NCS}\right]^{2+}\) may be determined by how darkly colored the solution is (measured by a spectrometer). In one such experiment, \(1.0 \mathrm{~mL}\) of \(0.20 \mathrm{M} \mathrm{Fe}\left(\mathrm{NO}_{3}\right)_{3}\) was mixed with \(1.0 \mathrm{~mL}\) of \(1.0 \times 10^{-3} M \mathrm{KSCN}\) and \(8.0 \mathrm{~mL}\) of dilute \(\mathrm{HNO}_{3}\). The color of the solution quantitatively indicated that the \(\left[\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{5} \mathrm{NCS}\right]^{2+}\) concentration was \(7.3 \times 10^{-5} M\). Calculate the formation constant for \(\left[\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{5} \mathrm{NCS}\right]^{2+}\)

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