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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.

Problem 2

Explain the difference between the σ and π MOs for homo- nuclear diatomic molecules. How are bonding and antibonding orbitals different? Why are there two π MOs and one σ MO? Why are the π MOs degenerate?

Problem 5

Draw the Lewis structure for HCN. Indicate the hybrid orbitals, and draw a picture showing all the bonds between the atoms, labeling each bond as σ or π.

Problem 6

Which is the more correct statement: "The methane molecule (CH4) is a tetrahedral molecule because it is sp3 hybridized" or "The methane molecule (CH_ 4) is sp3 hybridized because it is a tetrahedral molecule"? What, if anything, is the difference between these two statements?

Problem 8

What are the relationships among bond order, bond energy, and bond length? Which of these quantities can be measured?

Problem 9

The molecules N2 and 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 MOs in N2 and CO might be different.

Problem 10

Do lone pairs about a central atom affect the hybridization of the central atom? If so, how?

Problem 11

In the hybrid orbital model, compare and contrast σ bonds with π bonds. What orbitals form the σ bonds and what orbitals form the π bonds? Assume the z -axis is the internuclear axis.

Problem 12

In the molecular orbital model, compare and contrast σ bonds with π bonds. What orbitals form the σ bonds and what orbitals form the π bonds? Assume the z -axis is the internuclear axis.

Problem 13

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 (3d,4d,5d, or 6d) would sulfur use to form hybrid orbitals requiring d atomic orbitals? Answer the same question for arsenic and for iodine.

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