Chapter 4: Problem 1
What are molecular orbitals? How do they compare with atomic orbitals? Can you tell by the shape of the bonding and antibonding orbitals which is lower in energy? Explain.
Chapter 4: Problem 1
What are molecular orbitals? How do they compare with atomic orbitals? Can you tell by the shape of the bonding and antibonding orbitals which is lower in energy? Explain.
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Get started for freeDetermine the molecular structure and hybridization of the central atom \(X\) in the polyatomic ion \(X Y_{3}^{+}\) given the following information: A neutral atom of X contains 36 electrons, and the element Y makes an anion with a \(1-\) charge, which has the electron configuration \(1 s^{2} 2 s^{2} 2 p^{6}\).
Write Lewis structures and predict the molecular structures of the following. (See Exercises 25 and \(26 .\) ) a. \(\mathrm{OCl}_{2}, \mathrm{KrF}_{2}, \mathrm{BeH}_{2}, \mathrm{SO}_{2}\) b. \(\mathrm{SO}_{3}, \mathrm{NF}_{3}, \mathrm{IF}_{3}\) c. \(\mathrm{CF}_{4}, \mathrm{SeF}_{4}, \mathrm{KrF}_{4}\) d. IF \(_{5}, \mathrm{AsF}_{5}\) Which of these compounds are polar?
Compare and contrast the MO model with the local electron model. When is each useful?
Cyanamide \(\left(\mathrm{H}_{2} \mathrm{NCN}\right),\) an important industrial chemical, is produced by the following steps: Calcium cyanamide (CaNCN) is used as a direct-application fertilizer, weed killer, and cotton defoliant. It is also used to make cyanamide, dicyandiamide, and melamine plastics: a. Write Lewis structures for \(\mathrm{NCN}^{2-}, \mathrm{H}_{2} \mathrm{NCN}\), dicyandiamide, and melamine, including resonance structures where appropriate. b. Give the hybridization of the \(\mathrm{C}\) and \(\mathrm{N}\) atoms in each species. c. How many \(\sigma\) bonds and how many \(\pi\) bonds are in each species? d. Is the ring in melamine planar? e. There are three different \(\mathrm{C}-\mathrm{N}\) bond distances in dicyandiamide, NCNC(NH_)_2, and the molecule is nonlinear. Of all the resonance structures you drew for this molecule, predict which should be the most important.
Consider the following electron configuration: $$\left(\sigma_{3 s}\right)^{2}\left(\sigma_{3 s}^{* *}\right)^{2}\left(\sigma_{3 p}\right)^{2}\left(\pi_{3 p}\right)^{4}\left(\pi_{3 p}^{*}\right)^{4}$$ Give four species that, in theory, would have this electron configuration.
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