Chapter 10: Problem 46
Explain the significance of bond order. Can bond order be used for quantitative comparisons of the strengths of chemical bonds?
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Chapter 10: Problem 46
Explain the significance of bond order. Can bond order be used for quantitative comparisons of the strengths of chemical bonds?
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The geometries discussed in this chapter all lend themselves to fairly straightforward elucidation of bond angles. The exception is the tetrahedron, because its bond angles are hard to visualize. Consider the \(\mathrm{CCl}_{4}\) molecule, which has a tetrahedral geometry and is nonpolar. By equating the bond moment of a particular \(\mathrm{C}-\mathrm{Cl}\) bond to the resultant bond moments of the other three \(\mathrm{C}-\mathrm{Cl}\) bonds in opposite directions, show that the bond angles are all equal to \(109.5^{\circ}\)
Draw a potential energy curve for the bond formation in \(\mathrm{F}_{2}\).
Draw a molecular orbital energy level diagram for each of these species: \(\mathrm{He}_{2}, \mathrm{HHe}, \mathrm{He}_{2}^{+} .\) Compare their relative stabilities in terms of bond orders. (Treat HHe as a diatomic molecule with three electrons.)
Draw Lewis structures and give the other information requested for the following molecules: (a) \(\mathrm{BF}_{3}\). Shape: planar or nonplanar? (b) \(\mathrm{ClO}_{3}^{-}\). Shape: planar or nonplanar? (c) \(\mathrm{H}_{2} \mathrm{O}\). Show the direction of the resultant dipole moment. (d) \(\mathrm{OF}_{2}\). Polar or nonpolar molecule? (e) \(\mathrm{SeO}_{2}\). Estimate the OSeO bond angle.
Which of these pairs of atomic orbitals of adjacent nuclei can overlap to form a sigma bond? Which overlap to form a pi bond? Which cannot overlap (no bond)? Consider the \(x\) -axis to be the internuclear axis, that is, the line joining the nuclei of the two atoms. (a) \(1 s\) and \(1 s,\) (b) \(1 s\) and \(2 p_{x},\) (c) \(2 p_{x}\) and \(2 p_{y}\) (d) \(3 p_{y}\) and \(3 p_{y},\) (e) \(2 p_{x}\) and \(2 p_{x}\), (f) 1 s and 2 s.
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