Chapter 20: Problem 6
Why do transition metals have more oxidation states than other elements? Give the highest oxidation states for scandium to copper.
Chapter 20: Problem 6
Why do transition metals have more oxidation states than other elements? Give the highest oxidation states for scandium to copper.
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Get started for freeCopper 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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