Chapter 9: Problem 42
How would you expect the extent of overlap of atomic orbitals to vary in the series IF, ICl, \(\mathrm{IBr}\), and \(\mathrm{I}_{2}\) ?
Chapter 9: Problem 42
How would you expect the extent of overlap of atomic orbitals to vary in the series IF, ICl, \(\mathrm{IBr}\), and \(\mathrm{I}_{2}\) ?
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Get started for freeThe nitrogen atoms in \(\mathrm{N}_{2}\) participate in multiple bonding, whereas those in hydrazine, \(\mathrm{N}_{2} \mathrm{H}_{4}\), do not. (a) Draw Lewis structures for both molecules. (b) What is the hybridization of the nitrogen atoms in each molecule? (c) Which molecule has a stronger \(\mathrm{N}-\mathrm{N}\) bond?
Draw the Lewis structure for each of the following molecules or ions, and predict their electron-domain and molecular geometries: (a) \(\mathrm{PF}_{3}\), (b) \(\mathrm{CH}_{3}{ }^{+}\), (c) \(\mathrm{BrF}_{3}\), (d) \(\mathrm{ClO}_{4}^{-}(\mathrm{e}) \mathrm{XeF}_{2}\), (f) \(\mathrm{BrO}_{2}^{-}\).
(a) If the valence atomic orbitals of an atom are sp hybridized, how many unhybridized \(p\) orbitals remain in the valence shell? How many \(\pi\) bonds can the atom form? (b) Imagine that you could hold two atoms that are bonded together, twist them, and not change the bond length, Would it be easier to twist (rotate) around a single \(\sigma\) bond or around a double ( \(\sigma\) plus \(\pi\) ) bond, or would they be the same? Explain.
(a) What does the term paramagnetism mean? (b) How can one determine experimentally whether a substance is paramagnetic? (c) Which of the following ions would you expect to be paramagnetic: \(\mathrm{O}_{2}{ }^{+}, \mathrm{N}_{2}{ }^{2-}, \mathrm{Li}_{2}{ }^{+}, \mathrm{O}_{2}{ }^{2-} ?\) For those ions that are paramagnetic, determine the number of unpaired electrons.
Write the electron configuration for the first excited state for \(\mathrm{N}_{2}\) - that is, the state with the highest-energy electron moved to the next available energy level. (a) Is the nitrogen in its first excited state diamagnetic or paramagnetic? (b) Is the \(\mathrm{N}-\mathrm{N}\) bond strength in the first excited state stronger or weaker compared to that in the ground state? Explain.
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