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Chapter 3 Simple Bonding Theory
Lewis Dot Structures Resonance Formal Charge VSEPR: the subtle effects
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Lewis Dot Structures 1. Count valence electrons 2. Arrange atoms
3. Add bonds 4. Add lone pairs 5. Convert lone pairs to bonding pairs (octet rule and exceptions)
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Lewis Dot Structures Examples: CO2 SO3 N2O XeF4 ClF3 PCl6–
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Why does the octet rule work?
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More complex NO2 NO
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= Group # - #unshared electrons on atom - # bonds to atom
Formal Charge = Group # - #unshared electrons on atom - # bonds to atom Example: O3
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Resonance Example: SO3
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Resonance and Formal Charge
Example: SCN-
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Resonance and Formal Charge
Example: SCN-
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Octet Rule vs. Pi Bonding Trends
BeF2 and BF3
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Octet Rule vs. Formal Charge
Always follow octet rule Exceptions? SO42-
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VSEPR Maximize “personal space” CO2, SO3, SO42–, PCl5, SF6
Lone pairs vs. bonding pairs? Single bonds vs. multiple bonds? Electronegativity effects
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VSEPR
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Lone Pair Effects
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Pi Bonds vs. Lone Pairs: Guess these bond angles.
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Pi Bonds vs. Lone Pairs: Guess these bond angles.
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Pi Bonds vs. Lone Pairs
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Pi Bonds vs. Lone Pairs Which take up more room: lone pairs or a pi bond?
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Electronegativity Effects
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Electronegativity Effects
Molecule X-P-X Angle o PF PCl PBr Explain this trend.
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Electronegativity Effects
Molecule X-P-X Angle o PF PCl PBr Terminal Atom Effects: F: Electron density of the bond pairs is mostly near the F. Electron density near the central atom is less, which decreases bond pair – bond pair repulsion near the P.
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Electronegativity Effects
Molecule H-X-H Angle o H2O H2S H2Se Explain this trend.
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Electronegativity Effects
Molecule H-X-H Angle o H2O H2S H2Se Explain this trend. Central atom effects: O: as O pulls more electron density toward it, bonds have more electron density near the central atom. This causes greater bond pair – bond pair repulsions.
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Electronegativity Effects
Molecule X-As-X Angle o AsF3 AsCl3 AsBr3 Predict this trend.
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Predicting Positions of Different Atoms
PF3Cl Are Cl atoms axial or equatorial?
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Homework Chapter 3 7, 9 acde, 11, 12,14,29,30a
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