Chapter 9: Problem 71
Determine the electron configurations for \(\mathrm{CN}^{+}, \mathrm{CN}\), and \(\mathrm{CN}^{-}\). (a) Which species has the strongest \(\mathrm{C}-\mathrm{N}\) bond? (b) Which species, if any, has unpaired electrons?
Chapter 9: Problem 71
Determine the electron configurations for \(\mathrm{CN}^{+}, \mathrm{CN}\), and \(\mathrm{CN}^{-}\). (a) Which species has the strongest \(\mathrm{C}-\mathrm{N}\) bond? (b) Which species, if any, has unpaired electrons?
All the tools & learning materials you need for study success - in one app.
Get started for freeFor both atoms and molecules, ionization energies (Section 7.4) are related to the energies of orbitals: The lower the energy of the orbital, the greater the ionization energy. The first ionization energy of a molecule is therefore a measure of the energy of the highest occupied molecular orbital (HOMO). See the "Chemistry Put to Work" box on Orbitals and Energy. The first ionization energies of several diatomic molecules are given in electron-volts in the following table: \begin{tabular}{ll} \hline Molecule & \(I_{1}(\mathrm{eV})\) \\ \hline \(\mathrm{H}_{2}\) & \(15.4\) \\ \(\mathrm{~N}_{2}\) & \(15.6\) \\ \(\mathrm{O}_{2}\) & \(12.1\) \\ \(\mathrm{~F}_{2}\) & \(15.7\) \\ \hline \end{tabular} (a) Convert these ionization energies to \(\mathrm{kJ} / \mathrm{mol} .(\mathrm{b})\) On the same plot, graph \(I_{1}\) for the \(\mathrm{H}, \mathrm{N}, \mathrm{O}\), and \(\mathrm{F}\) atoms (Figure 7.11) and \(I_{1}\) for the molecules listed. (c) Do the ionization energies of the molecules follow the same periodic trends as the ionization energies of the atoms? (d) Use molecular orbital energy-level diagrams to explain the trends in the ionization energies of the molecules.
(a) What is the probability of finding an electron on the internuclear axis if the electron occupies a \(\pi\) molecular orbital? (b) For a homonuclear diatomic molecule, what similarities and differences are there between the \(\pi_{2 p}\) MO made from the \(2 p_{x}\) atomic orbitals and the \(\pi_{2 p}\) MO made from the \(2 p_{y}\) atomic orbitals? (c) Why are the \(\pi_{2 p}\) MOs lower in energy than the \(\pi_{2 p}^{*}\) MOs?
Predict the trend in the \(\mathrm{F}(\) axial \()-\mathrm{A}-\mathrm{F}\) (equatorial) bond angle in the following \(\mathrm{AF}_{n}\) molecules: \(\mathrm{PF}_{5}, \mathrm{SF}_{4}\) and \(\mathrm{ClF}_{3}\)
The molecules \(\mathrm{SiF}_{4}, \mathrm{SF}_{4}\), and \(\mathrm{XeF}_{4}\) have molecular formulas of the type \(\mathrm{AF}_{4}\), but the molecules have different molecular geometries. Predict the shape of each molecule, and explain why the shapes differ.
Consider the molecule \(\mathrm{PF}_{4} \mathrm{Cl}\). (a) Draw a Lewis structure for the molecule, and predict its electron-domain geometry. (b) Which would you expect to take up more space, a. \(\mathrm{P}-\mathrm{F}\) bond or a \(\mathrm{P}-\mathrm{Cl}\) bond? Explain. (c) Predict the molecular geometry of \(\mathrm{PF}_{4} \mathrm{Cl}\). How did your answer for part (b) influence your answer here in part (c)? (d) Would you expect the molecule to distort from its ideal electron-domain geometry? If so, how would it distort?
What do you think about this solution?
We value your feedback to improve our textbook solutions.