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Ch.9 - Molecular Geometry and Bonding Theories
Chapter 9, Problem 110

a) Using only the valence atomic orbitals of a hydrogen atom and a fluorine atom, and following the model of Figure 9.46, how many MOs would you expect for the HF molecule? Molecular orbital diagram showing energy levels for N and O atoms in the NO molecule.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Molecular Orbitals (MOs)

Molecular orbitals are formed when atomic orbitals combine during the formation of a molecule. In the case of diatomic molecules like HF, the valence atomic orbitals of hydrogen and fluorine combine to create bonding and antibonding molecular orbitals. The number of MOs formed is equal to the sum of the atomic orbitals involved, which helps in understanding the electronic structure and stability of the molecule.
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Valence Atomic Orbitals

Valence atomic orbitals are the outermost orbitals of an atom that participate in chemical bonding. For hydrogen, the valence orbital is the 1s orbital, while for fluorine, it includes the 2s and 2p orbitals. Understanding these orbitals is crucial for predicting how atoms will interact and bond to form molecules, such as HF.
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Bonding and Antibonding Orbitals

In molecular orbital theory, bonding orbitals are lower in energy and stabilize the molecule, while antibonding orbitals are higher in energy and can destabilize it. When atomic orbitals combine, the resulting MOs include both types. For HF, the bonding orbital formed from the combination of hydrogen's 1s and fluorine's 2p orbitals will contribute to the molecule's stability, while any antibonding orbitals formed will have the opposite effect.
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Related Practice
Textbook Question

Place the following molecules and ions in order from smallest to largest bond order: N22+, He2+, Cl2 H2-, O22-.

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Textbook Question
Molecules that are brightly colored have a small energy gap between filled and empty electronic states (the HOMOLUMO gap; see Exercise 9.104). Suppose you have two samples, one is lycopene which is responsible for the red color in tomato, and the other is curcumin which is responsible for the yellow color in turmeric. Which one has the larger HOMO-LUMO gap?
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Textbook Question

Azo dyes are organic dyes that are used for many applications, such as the coloring of fabrics. Many azo dyes are derivatives of the organic substance azobenzene, C12H10N2. A closely related substance is hydrazobenzene, C12H12N2. The Lewis structures of these two substances are

(Recall the shorthand notation used for benzene.) (c) Predict the N¬N¬C angles in each of the substances.

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Textbook Question

Carbon monoxide, CO, is isoelectronic to N2. (d) Would you expect the p2p MOs of CO to have equal atomic orbital contributions from the C and O atoms? If not, which atom would have the greater contribution?

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Textbook Question

The energy-level diagram in Figure 9.36 shows that the sideways overlap of a pair of p orbitals produces two molecular orbitals, one bonding and one antibonding. In ethylene there is a pair of electrons in the bonding π orbital between the two carbons. Absorption of a photon of the appropriate wavelength can result in promotion of one of the bonding electrons from the p2p to the p*2p molecular orbital. (a) Assuming this electronic transition corresponds to the HOMO-LUMO transition, what is the HOMO in ethylene?

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Textbook Question

The energy-level diagram in Figure 9.36 shows that the sideways overlap of a pair of p orbitals produces two molecular orbitals, one bonding and one antibonding. In ethylene there is a pair of electrons in the bonding π orbital between the two carbons. Absorption of a photon of the appropriate wavelength can result in promotion of one of the bonding electrons from the p2p to the p*2p molecular orbital. (b) Assuming this electronic transition corresponds to the HOMO-LUMO transition, what is the LUMO in ethylene?

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