Chapter 4: Problem 67
Using molecular orbital theory, explain why the removal of one electron in \(\mathrm{O}_{2}\) strengthens bonding, while the removal of one electron in \(\mathrm{N}_{2}\) weakens bonding.
Chapter 4: Problem 67
Using molecular orbital theory, explain why the removal of one electron in \(\mathrm{O}_{2}\) strengthens bonding, while the removal of one electron in \(\mathrm{N}_{2}\) weakens bonding.
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Get started for freePredict the molecular structure (including bond angles) for each of the following. (See Exercises 25 and \(26 .\) ) a. ICls b. \(\mathrm{XeCl}_{4}\) c. \(\mathrm{SeCl}_{6}\)
Why are \(d\) orbitals sometimes used to form hybrid orbitals? Which period of elements does not use \(d\) orbitals for hybridization? If necessary, which \(d\) orbitals \((3 d, 4 d, 5 d, \text { or } 6 d)\) would sulfur use to form hybrid orbitals requiring \(d\) atomic orbitals? Answer the same question for arsenic and for iodine.
The allene molecule has the following Lewis structure: Must all hydrogen atoms lie the same plane? If not, what is their spatial relationship? Explain.
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Biacetyl and acetoin are added to margarine to make it taste more like butter. Complete the Lewis structures, predict values for all \(\mathrm{C}-\mathrm{C}-\mathrm{O}\) bond angles, and give the hybridization of the carbon atoms in these two compounds. Must the four carbon atoms and two oxygen atoms in biacetyl lie in the same plane? How many \(\sigma\) bonds and how many \(\pi\) bonds are there in biacetyl and acetoin?
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