Chapter 3: Chemical Bonding Compounds are formed from
Transcription
Chapter 3: Chemical Bonding Compounds are formed from
The Octet Rule Atoms tend to lose, gain, or share electrons until they have eight valence electrons Chapter 3: Chemical Bonding Compounds are formed from chemically bound atoms or ions Bonding involves only the valence electrons Ionic compounds – ionic radii and lattice energies Molecular compounds – covalent (polar or non-polar) bond – bond order – bond strength – Lewis structures Lewis Symbols – show the valence electrons as dots around the atomic symbol 1 2 3 4 1 Bond strength Bond orders and bond distances Bond dissociation energy (the energy required to break a bond) Single bond distances Bond distances of other bond types 5 6 7 8 /mol 2 9 10 11 12 3 13 One more example: HNO3 (HONO2) 14 O Concept of Resonance N O O 24e O H O O H More than one possible Lewis structures. The actual structure of a molecule is taken as a blend of all the feasible Lewis structures or N N O O O H do not confuse with structural isomers O N O O H Exceptions to the octet rule Elements in the 2nd period can never have more than 8 electrons Elements in the 3rd or higher periods can have more than 8 electrons N O O N O Odd-electron molecules Incomplete octet Expanded octet 15 16 4 What does writing resonance structures accomplish? Electrons are often delocalized between two or more atoms. Electrons in a single Lewis structure are assigned to a specific atom. Therefore, a single Lewis structure is insufficient to electron delocalization. Composite of resonance structures more accurately depicts electron distribution and describes a molecule. 17 18 Concept of formal charge Take SCN- as an example illustrating the importance of the formal charge concept (Don't confuse the formal charge with the oxidation state or the charge on an atom) More examples to show the application (formal charge and expanded octet 19 20 5 Octet Lewis Structure Expanded Octet Lewis Structure Formal Atom Charge Formal Atom Charge Expanded to SNF 3 F S F S 2+ N 2- F S Cl S 2- O O S O S 2+ O 1- Cl O O S XeO3 O 0 0 S O S 0 O 0 Cl 12 12 O O S 2+ O 1- O S O S 0 O 0, 1- 12 O O SO32- S N An atom that has a d subshell in the valence electron shell can accommodate more than an octet of electrons O O Cl SO4 F F F SO2Cl2 Expanded octet N N O O S 1+ O 1- Xe 3+ O 1- O O S O S 0 O 0, 1- 10 O Xe O IOF5 O Xe F I 1+ F F O 1- F I F F 0 0 F I 0 F O 0 14 Hypervalence: Hypervalent molecules: species having more than an octet around at least one atom O O F Xe O O I 14 F 21 22 VSEPR model (Valence Shell Electron Pair Repulsions) Molecular geometry The most stable arrangement of groups attached to a central atom is the one that has the maximum separation of electron pairs (bonded or non-bonded) The properties of a compound are very much determined by the size and shape of its molecules. 23 24 6 Electron-pair geometry Molecules in which the central atom has no lone pairs 25 Molecules in which the central atom has one or more lone pairs 26 Using the examples to illustrate the VSEPR model SF4 , BrF3, XeF2, XeF4, OSF4 CH4 NH3 OH2 27 28 7 Using the examples to illustrate the VSEPR model SF4 , BrF3, XeF2, XeF4, OSF4 F F F S F S F F F F F F F F Br Br F F F Br F F F F F Xe F Xe Xe F Xe F F F F F F F F S F F F Xe F F SF4 adopts a seesaw structure 29 30 Guidelines for applying the VSEPR model 31 32 8 Valence Bond Theory describes covalent bond in terms of the overlap of atomic orbitals Valence bond model of H2 33 34 Hybridization -- Hybrid orbitals Valence bond theory and molecular geometry Hybrid orbitals are mixtures of atomic orbitals with intermediate energy The number of s, p and d orbitals in the mixture equals the number of hybrid orbitals 35 36 9 37 38 39 40 10 Examples with an sp3 hybridization central atom Examples: PCl5, SF4, OSF4 Hybridization of s, p and d orbitals Examples: SF6, XeF4 Pentagonal bipyramidal Geometry (sp3d3) 41 IF7 42 Hybridization in ethylene, acetylene, etc. Concept of σ and π bonds Bonds that result from σ overlap are called σ bonds. Bonds that result from π overlap are called π bonds. 43 44 11 Structure of Ethylene 45 46 Bond polarity and dipole moment 47 48 12 49 50 Molecular Dipole Moments Molecule must have polar bonds (necessary but not sufficient) Need to know molecular shape because individual bond dipoles can cancel Examples 51 13