Chapter 9: Problem 11
In the hybrid orbital model, compare and contrast \(\sigma\) bonds with \(\pi\) bonds. What orbitals form the \(\sigma\) bonds and what orbitals form the \(\pi\) bonds? Assume the \(z\) -axis is the internuclear axis.
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Chapter 9: Problem 11
In the hybrid orbital model, compare and contrast \(\sigma\) bonds with \(\pi\) bonds. What orbitals form the \(\sigma\) bonds and what orbitals form the \(\pi\) bonds? Assume the \(z\) -axis is the internuclear axis.
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What are the relationships among bond order, bond energy, and bond length? Which of these quantities can be measured?
The atoms in a single bond can rotate about the internuclear axis without breaking the bond. The atoms in a double and triple bond cannot rotate about the internuclear axis unless the bond is broken. Why?
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.
In which of the following diatomic molecules would the bond strength be expected to weaken as an electron is removed? $$ \begin{array}{ll}{\text { a. } H_{2}} & {\text { c. } C_{2}^{2-}} \\ {\text { b. } B_{2}} & {\text { d. OF }}\end{array} $$
The molecules \(\mathrm{N}_{2}\) and \(\mathrm{CO}\) are isoelectronic but their properties are quite different. Although as a first approximation we often use the same MO diagram for both, suggest how the \(\mathrm{MOs}\) in \(\mathrm{N}_{2}\) and \(\mathrm{CO}\) might be different.
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