Chapter 23: Problem 47
Is it possible for a low-spin octahedral Fe(II) complex to be paramagnetic? Explain.
Chapter 23: Problem 47
Is it possible for a low-spin octahedral Fe(II) complex to be paramagnetic? Explain.
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Get started for freeWrite the formula for each of the following compounds, being sure to use brackets to indicate the coordination sphere: (a) hexaamminechromium(III) nitrate (b) tetraamminecarbonatocobalt(III) sulfate (c) dichlorobis(ethylenediamine) platinum(IV) bromide (d) potassium diaquatetrabromovanadate(III) (e) bis(ethylenediamine) zinc(II) tetraiodomercurate(II)
When Alfred Werner was developing the field of coordination chemistry, it was argued by some that the optical activity he observed in the chiral complexes he had prepared was because of the presence of carbon atoms in the molecule. To disprove this argument, Werner synthesized a chiral complex of cobalt that had no carbon atoms in it, and he was able to resolve it into its enantiomers. Design a cobalt(III) complex that would be chiral if it could be synthesized and that contains no carbon atoms. (It may not be possible to synthesize the complex you design, but we won't worry about that for now.)
The value of \(\Delta\) for the \(\left[\mathrm{CrF}_{6}\right]^{3-}\) complex is \(182 \mathrm{~kJ} / \mathrm{mol}\). Calculate the expected wavelength of the absorption corresponding to promotion of an electron from the lowerenergy to the higher-energy \(d\) -orbital set in this complex. Should the complex absorb in the visible range?
Explain why the \(d_{x y}, d_{x z}\), and \(d_{y z}\) orbitals lie lower in energy than the \(d_{z}^{2}\) and \(d_{x^{2}-y^{2}}\) orbitals in the presence of an octahedral arrangement of ligands about the central metal ion.
The +2 oxidation state is common for almost all the transition metals. Suggest an explanation.
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