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?

Short Answer

Expert verified
The expected wavelength of absorption for the \(\left[\mathrm{CrF}_{6}\right]^{3-}\) complex is \(6.57 \times 10^{-7}\text{ m}\), which falls within the visible range (380 nm to 760 nm). Thus, the complex should absorb in the visible range.

Step by step solution

01

Calculate the energy of photon

The energy of the photon is given by the value of \(\Delta = 182 \mathrm{~kJ/mol}\). We'll first convert this energy from kJ to J. Multiply by 1000 to get the energy in J/mol: \[ \Delta = 182 \times 1000 \mathrm{~J/mol} = 182000 \mathrm{~J/mol} \]
02

Convert energy per mole to energy per photon

Next, we need to convert the energy per mole to the energy per photon. To do this, divide the energy in J/mol by Avogadro's number, \(N_A = 6.022 \times 10^{23} \text{ mol}^{-1} \). This will give us the energy in J/photon: \[ \Delta = \frac{182000 \mathrm{~J/mol}}{6.022 \times 10^{23} \text{ mol}^{-1}} = 3.02 \times 10^{-19} \mathrm{~J/photon} \]
03

Use Planck's equation to find the wavelength

Planck's equation relates energy (\(E\)), frequency (\(\nu\)), and wavelength (\(\lambda\)) by: \[ E = h \nu = \frac{hc}{\lambda} \] Here, \(h\) is the Planck's constant (\(h = 6.626 \times 10^{-34} \text{ J} \cdot \text{s}\)) and \(c\) is the speed of light in a vacuum (\(c = 2.998 \times 10^8 \text{ m/s} \)). We need to find the wavelength (\(\lambda\)) corresponding to the energy (\(E = 3.02 \times 10^{-19} \text{ J/photon}\)). Rearranging Planck's equation gives: \[ \lambda = \frac{hc}{E} \] Now, substitute the values of \(E\), \(h\), and \(c\) to find the wavelength: \[ \lambda = \frac{6.626 \times 10^{-34} \text{ J} \cdot \text{s} \times 2.998 \times 10^8 \text{ m/s}}{3.02 \times 10^{-19} \text{ J/photon}} = 6.57 \times 10^{-7} \text{ m} \]
04

Determine if the complex absorbs in the visible range

The visible range of light falls between 380 nm and 760 nm (3.80 x 10^{-7} m and 7.60 x 10^{-7} m). The calculated wavelength for the chromium hexafluoride complex is 6.57 x 10^{-7} m, which falls within the visible range. Therefore, the complex should absorb in the visible range.

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Most popular questions from this chapter

(a) What is the meaning of the term coordination number as it applies to metal complexes? (b) Give an example of a ligand that is neutral and one that is negatively charged. (c) Would you expect ligands that are positively charged to be common? Explain. (d) What type of chemical bonding is characteristic of coordination compounds? Illustrate with the compound \(\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{6} \mathrm{Cl}_{3}\) (e) What are the most common coordination numbers for metal complexes?

Carbon monoxide is toxic because it binds more strongly to the iron in hemoglobin (Hb) than does \(\mathrm{O}_{2}\), as indicated by these approximate standard free-energy changes in blood: $$ \begin{array}{ll} \mathrm{Hb}+\mathrm{O}_{2} \longrightarrow \mathrm{HbO}_{2} & \Delta G^{\circ}=-70 \mathrm{~kJ} \\\ \mathrm{Hb}+\mathrm{CO} \longrightarrow \mathrm{HbCO} & \Delta G^{\circ}=-80 \mathrm{~kJ} \end{array} $$ Using these data, estimate the equilibrium constant at \(298 \mathrm{~K}\) for the equilibrium $$ \mathrm{HbO}_{2}+\mathrm{CO} \rightleftharpoons \mathrm{HbCO}+\mathrm{O}_{2} $$

Give the number of (valence) \(d\) electrons associated with the central metal ion in each of the following complexes: (a) \(\mathrm{K}_{3}\left[\mathrm{Fe}(\mathrm{CN})_{6}\right]\), (b) \(\left[\mathrm{Mn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]\left(\mathrm{NO}_{3}\right)_{2}\) (c) \(\mathrm{Na}\left[\mathrm{Ag}(\mathrm{CN})_{2}\right]\) (d) \(\left[\mathrm{Cr}\left(\mathrm{NH}_{3}\right)_{4} \mathrm{Br}_{2}\right] \mathrm{ClO}_{4}\), (e) \([\mathrm{Sr}(\mathrm{EDTA})]^{2-}\)

Draw the crystal-field energy-level diagrams and show the placement of \(d\) electrons for each of the following: (a) \(\left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+}\) (four unpaired electrons), (b) \(\left[\mathrm{Mn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+}\) (high spin), (c) \(\left[\mathrm{Ru}\left(\mathrm{NH}_{3}\right)_{5} \mathrm{H}_{2} \mathrm{O}\right]^{2+}\) (low spin), (d) \(\left[\operatorname{Ir} \mathrm{Cl}_{6}\right]^{2-}\) (low spin), (e) \(\left[\mathrm{Cr}(\mathrm{en})_{3}\right]^{3+},(\mathrm{f})\left[\mathrm{NiF}_{6}\right]^{4-}\)

Sketch the structure of the complex in each of the following compounds and give the full compound name: (a) cis- \(\left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{4}\left(\mathrm{H}_{2} \mathrm{O}\right)_{2}\right]\left(\mathrm{NO}_{3}\right)_{2}\) (b) \(\mathrm{Na}_{2}\left[\mathrm{Ru}\left(\mathrm{H}_{2} \mathrm{O}\right) \mathrm{Cl}_{5}\right]\) (c) trans- \(\mathrm{NH}_{4}\left[\mathrm{Co}\left(\mathrm{C}_{2} \mathrm{O}_{4}\right)_{2}\left(\mathrm{H}_{2} \mathrm{O}\right)_{2}\right]\) (d) cis- \(\left[\mathrm{Ru}(\mathrm{en})_{2} \mathrm{Cl}_{2}\right]\)

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