© Copyright Pearson Prentice Hall Molecular Compounds > Slide 1 of 18 8.3 Molecular Orbitals How are atomic and molecular orbitals related? When two atoms.

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Presentation transcript:

© Copyright Pearson Prentice Hall Molecular Compounds > Slide 1 of Molecular Orbitals How are atomic and molecular orbitals related? When two atoms combine, the molecular orbital model assumes that their atomic orbitals overlap to produce molecular orbitals, or orbitals that apply to the entire molecule.

Slide 2 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.3 Molecular Orbitals Just as an atomic orbital belongs to a particular atom, a molecular orbital belongs to a molecule as a whole. A molecular orbital that can be occupied by two electrons of a covalent bond is called a bonding orbital.

Slide 3 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.3 Molecular Orbitals Sigma Bonds When two atomic orbitals combine to form a molecular orbital that is symmetrical around the axis connecting two atomic nuclei, a sigma bond is formed.

Slide 4 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.3 Molecular Orbitals A Sigma Bond

Slide 5 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.3 Molecular Orbitals When two fluorine atoms combine, the p orbitals overlap to produce a bonding molecular orbital. The F—F bond is a sigma bond.

Slide 6 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.3 Molecular Orbitals Pi Bonds In a pi bond (symbolized by the Greek letter  ), the bonding electrons are most likely to be found in sausage-shaped regions above and below the bond axis of the bonded atoms.

© Copyright Pearson Prentice Hall Slide 7 of 28 Bonding Theories > 8.3 Molecular Orbitals Pi-bonding Molecular Orbital

© Copyright Pearson Prentice Hall Bonding Theories > Slide 8 of VSEPR Theory How does VSEPR theory help predict the shapes of molecules?

Slide 9 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.3 VSEPR Theory The hydrogens in a methane molecule are at the four corners of a geometric solid. All of the H—C—H angles are 109.5°, the tetrahedral angle.

Slide 10 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.3 VSEPR Theory The valence-shell electron-pair repulsion theory, or VSEPR theory, explains the three- dimensional shape of methane. According to VSEPR theory, the repulsion between electron pairs causes molecular shapes to adjust so that the valence- electron pairs stay as far apart as possible.

Slide 11 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.3 VSEPR Theory The measured H—N—H bond angle is only 107°.

Slide 12 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.3 VSEPR Theory The measured bond angle in water is about 105°.

Slide 13 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.3 VSEPR Theory The carbon dioxide molecule is linear.

Slide 14 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.3 VSEPR Theory Nine Possible Molecular Shapes

© Copyright Pearson Prentice Hall Bonding Theories > Slide 15 of Hybrid Orbitals Orbital hybridization provides information about both molecular bonding and molecular shape. In hybridization, several atomic orbitals mix to form the same total number of equivalent hybrid orbitals.

© Copyright Pearson Prentice Hall Slide 16 of 28 Bonding Theories > 8.3 Hybrid Orbitals Hybridization Involving Single Bonds

© Copyright Pearson Prentice Hall Slide 17 of 28 Bonding Theories > 8.3 Hybrid Orbitals Hybridization Involving Double Bonds

Slide 18 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.3 Hybrid Orbitals Hybridization Involving Triple Bonds

Slide 19 of 28 © Copyright Pearson Prentice Hall Bonding Theories > Bond Polarity

Slide 20 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.4 Bond Polarity How do you determine the charge distribution in a polar bond? When the atoms in a bond pull equally (as occurs when identical atoms are bonded), the bonding electrons are shared equally, and the bond is a nonpolar covalent bond.

Slide 21 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.4 Bond Polarity The bonding pairs of electrons in covalent bonds are pulled by the nuclei.

Slide 22 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.4 Bond Polarity The chlorine atom attracts the electron cloud more than the hydrogen atom does.

Slide 23 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.4 Bond Polarity A polar covalent bond, known also as a polar bond, is a covalent bond between atoms in which the electrons are shared unequally. The more electronegative atom attracts electrons more strongly and gains a slightly negative charge. The less electronegative atom has a slightly positive charge.

Slide 24 of 28 © Copyright Pearson Prentice Hall Bonding Theories > Bond Polarity 8.4

Slide 25 of 28 © Copyright Pearson Prentice Hall Bonding Theories > Polar Molecules 8.4 In a polar molecule, one end of the molecule is slightly negative and the other end is slightly positive. A molecule that has two poles is called a dipolar molecule, or dipole. What happens to polar molecules between a pair of oppositely charged metal plates?

Slide 26 of 28 © Copyright Pearson Prentice Hall Bonding Theories > Polar Molecules A hydrogen chloride molecule is a dipole. 8.4

Slide 27 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.4 Attractions Between Molecules What are intermolecular attractions & how do they compare with ionic and covalent bonds?

Slide 28 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.4 Attractions Between Molecules Intermolecular attractions are weaker than either ionic or covalent bonds. These attractions are responsible for determining whether a molecular compound is a gas, a liquid, or a solid at a given temperature. Van der Waals Forces & Hydrogen bonding

Slide 29 of 28 © Copyright Pearson Prentice Hall Bonding Theories > Attractions Between Molecules Van der Waals Forces The two weakest attractions between molecules are collectively called van der Waals forces, named after the Dutch chemist Johannes van der Waals (1837–1923). 8.4

Slide 30 of 28 © Copyright Pearson Prentice Hall Bonding Theories > Attractions Between Molecules Dipole interactions occur when polar molecules are attracted to one another. 8.4

Slide 31 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.4 Attractions Between Molecules Dispersion forces, the weakest of all molecular interactions, are caused by the motion of electrons. The strength of dispersion forces generally increases as the number of electrons in a molecule increases.

Slide 32 of 28 © Copyright Pearson Prentice Hall Bonding Theories > Attractions Between Molecules Hydrogen Bonds Hydrogen bonds are attractive forces in which a hydrogen covalently bonded to a very electronegative atom is also weakly bonded to an unshared electron pair of another electronegative atom. 8.4

Slide 33 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.4 Attractions Between Molecules Hydrogen Bonding in Water

Slide 34 of 28 © Copyright Pearson Prentice Hall Bonding Theories > Attractions Between Molecules The relatively strong attractive forces between water molecules cause the water to form small drops on a waxy surface. 8.4

Slide 35 of 28 © Copyright Pearson Prentice Hall Bonding Theories > Intermolecular Attractions and Molecular Properties 8.4 Network solids (or network crystals) are solids in which all of the atoms are covalently bonded to each other. Network solids consist of molecules that do not melt until the temperature reaches 1000°C or higher, or they decompose without melting at all.

Slide 36 of 28 © Copyright Pearson Prentice Hall Bonding Theories > Intermolecular Properties and Molecular Properties Melting a network solid would require breaking covalent bonds throughout the solid. 8.4

Slide 37 of 28 © Copyright Pearson Prentice Hall Bonding Theories > 8.4 Intermolecular Attractions and Molecular Properties Diamond is an example of a network solid. Diamond does not melt. It vaporizes to a gas at 3500°C or above.

Slide 38 of 28 © Copyright Pearson Prentice Hall Bonding Theories > Intermolecular Attractions and Molecular Properties 8.4