Chapter 9 Covalent Bonding: Orbitals
Copyright © Cengage Learning. All rights reserved 2 Draw the Lewis structure for methane, CH 4. –What is the shape of a methane molecule? tetrahedral –What are the bond angles? o EXERCISE!
Copyright © Cengage Learning. All rights reserved 3 What is the valence electron configuration of a carbon atom? s2p2 s2p2 Why can’t the bonding orbitals for methane be formed by an overlap of atomic orbitals? CONCEPT CHECK!
Copyright © Cengage Learning. All rights reserved 4 Bonding in Methane Assume that the carbon atom has four equivalent atomic orbitals, arranged tetrahedrally.
Copyright © Cengage Learning. All rights reserved 5 Hybridization Mixing of the native atomic orbitals to form special orbitals for bonding.
Copyright © Cengage Learning. All rights reserved 6 sp 3 Hybridization Combination of one s and three p orbitals. Whenever a set of equivalent tetrahedral atomic orbitals is required by an atom, the localized electron model assumes that the atom adopts a set of sp 3 orbitals; the atom becomes sp 3 hybridized. The four orbitals are identical in shape.
Hybridization – mixing of two or more atomic orbitals to form a new set of hybrid orbitals. 1.Mix at least 2 nonequivalent atomic orbitals (e.g. s and p). Hybrid orbitals have very different shape from original atomic orbitals. 2.Number of hybrid orbitals is equal to number of pure atomic orbitals used in the hybridization process. 3.Covalent bonds are formed by: a.Overlap of hybrid orbitals with atomic orbitals b.Overlap of hybrid orbitals with other hybrid orbitals
Hybrid Orbitals Hybrid orbitals are orbitals used to describe bonding that are obtained by taking combinations of atomic orbitals of an isolated atom. In this case, a set of hybrids are constructed from one “s” orbital and three “p” orbitals, so they are called sp 3 hybrid orbitals. The four sp 3 hybrid orbitals take the shape of a tetrahedron.
Copyright © Cengage Learning. All rights reserved 9 An Energy-Level Diagram Showing the Formation of Four sp 3 Orbitals
Formation of sp 3 Hybrid Orbitals
SP3 Hybridization c-chemistry/gen-chem- review/hybridization/v/sp3-hybridized- orbitals-and-sigma-bonds
Copyright © Cengage Learning. All rights reserved 13 Draw the Lewis structure for C 2 H 4 (ethylene)? –What is the shape of an ethylene molecule? trigonal planar around each carbon atom –What are the approximate bond angles around the carbon atoms? 120 o EXERCISE!
Copyright © Cengage Learning. All rights reserved 14 Why can’t sp 3 hybridization account for the ethylene molecule? CONCEPT CHECK!
Copyright © Cengage Learning. All rights reserved 15 sp 2 Hybridization Combination of one s and two p orbitals. Gives a trigonal planar arrangement of atomic orbitals. One p orbital is not used. –Oriented perpendicular to the plane of the sp 2 orbitals.
Formation of sp 2 Hybrid Orbitals
Copyright © Cengage Learning. All rights reserved 17 Sigma ( Σ ) Bond Electron pair is shared in an area centered on a line running between the atoms.
Copyright © Cengage Learning. All rights reserved 18 Pi ( Π ) Bond Forms double and triple bonds by sharing electron pair(s) in the space above and below the σ bond. Uses the unhybridized p orbitals.
Multiple Bonding To describe the multiple bonding in ethene, we must first distinguish between two kinds of bonds. A (sigma) bond is a “head-to-head” overlap of orbitals with a cylindrical shape about the bond axis. This occurs when two “s” orbitals overlap or “p” orbitals overlap along their axis. A (pi) bond is a “side-to-side” overlap of parallel “p” orbitals, creating an electron distribution above and below the bond axis.
Multiple Bonding Now imagine that the atoms of ethene move into position. Two of the sp 2 hybrid orbitals of each carbon overlap with the 1s orbitals of the hydrogens. The remaining sp 2 hybrid orbital on each carbon overlap to form a bond.
Multiple Bonding The remaining “unhybridized” 2p orbitals on each of the carbon atoms overlap side-to-side forming a bond. You therefore describe the carbon-carbon double bond as one bond and one bond.
Sigma bond ( ) – electron density between the 2 atoms Pi bond ( ) – electron density above and below plane of nuclei of the bonding atoms
Copyright © Cengage Learning. All rights reserved 25 An Orbital Energy-Level Diagram for sp 2 Hybridization
Copyright © Cengage Learning. All rights reserved 26 The Hybridization of the s, p x, and p y Atomic Orbitals
Formation of C=C Double Bond in Ethylene Copyright © Cengage Learning. All rights reserved 27 To play movie you must be in Slide Show Mode PC Users: Please wait for content to load, then click to play Mac Users: CLICK HERECLICK HERE
Copyright © Cengage Learning. All rights reserved 28 Draw the Lewis structure for CO 2. –What is the shape of a carbon dioxide molecule? linear –What are the bond angles? 180 o EXERCISE!
Copyright © Cengage Learning. All rights reserved 29 sp Hybridization Combination of one s and one p orbital. Gives a linear arrangement of atomic orbitals. Two p orbitals are not used. –Needed to form the π bonds.
Formation of sp Hybrid Orbitals
Copyright © Cengage Learning. All rights reserved 31 The Orbital Energy-Level Diagram for the Formation of sp Hybrid Orbitals on Carbon
Copyright © Cengage Learning. All rights reserved 32 When One s Orbital and One p Orbital are Hybridized, a Set of Two sp Orbitals Oriented at 180 Degrees Results
Copyright © Cengage Learning. All rights reserved 33 The Orbitals for CO 2
Copyright © Cengage Learning. All rights reserved 34 Draw the Lewis structure for PCl 5. –What is the shape of a phosphorus pentachloride molecule? trigonal bipyramidal –What are the bond angles? 90 o and 120 o EXERCISE!
Copyright © Cengage Learning. All rights reserved 35 dsp 3 Hybridization Combination of one d, one s, and three p orbitals. Gives a trigonal bipyramidal arrangement of five equivalent hybrid orbitals.
Copyright © Cengage Learning. All rights reserved 36 The Orbitals Used to Form the Bonds in PCl 5
Copyright © Cengage Learning. All rights reserved 37 Draw the Lewis structure for XeF 4. –What is the shape of a xenon tetrafluoride molecule? octahedral –What are the bond angles? 90 o and 180 o EXERCISE!
Copyright © Cengage Learning. All rights reserved 38 d 2 sp 3 Hybridization Combination of two d, one s, and three p orbitals. Gives an octahedral arrangement of six equivalent hybrid orbitals.
Copyright © Cengage Learning. All rights reserved 39 How is the Xenon Atom in XeF 4 Hybridized?
Copyright © Cengage Learning. All rights reserved 40 Draw the Lewis structure for HCN. Which hybrid orbitals are used? Draw HCN: –Showing all bonds between atoms. –Labeling each bond as σ or π. CONCEPT CHECK!
Determine the bond angle and expected hybridization of the central atom for each of the following molecules: NH 3 SO 2 KrF 2 CO 2 ICl 5 NH 3 – o, sp 3 SO 2 – 120 o, sp 2 KrF 2 – 90 o, 120 o, dsp 3 CO 2 – 180 o, sp ICl 5 – 90 o, 180 o, d 2 sp 3 CONCEPT CHECK!
# of Lone Pairs + # of Bonded Atoms HybridizationExamples sp sp 2 sp 3 sp 3 d sp 3 d 2 BeCl 2 BF 3 CH 4, NH 3, H 2 O PCl 5 SF 6 How do I predict the hybridization of the central atom? 1.Draw the Lewis structure of the molecule. 2.Count the number of lone pairs AND the number of atoms bonded to the central atom
Hybrid Orbitals Geometric Arrangements Number of Orbitals Example spLinear2Be in BeF 2 sp 2 Trigonal planar3B in BF 3 sp 3 Tetrahedral4C in CH 4 sp 3 dTrigonal bipyramidal5P in PCl 5 sp 3 d 2 Octahedral6S in SF 6
Copyright © Cengage Learning. All rights reserved 44 Using the Localized Electron Model Draw the Lewis structure(s). Determine the arrangement of electron pairs using the VSEPR model. Specify the hybrid orbitals needed to accommodate the electron pairs.
Regards a molecule as a collection of nuclei and electrons, where the electrons are assumed to occupy orbitals much as they do in atoms, but having the orbitals extend over the entire molecule. The electrons are assumed to be delocalized rather than always located between a given pair of atoms. Copyright © Cengage Learning. All rights reserved 45
The electron probability of both molecular orbitals is centered along the line passing through the two nuclei. –Sigma (σ) molecular orbitals (MOs) In the molecule only the molecular orbitals are available for occupation by electrons. Copyright © Cengage Learning. All rights reserved 46
Molecular Orbital Theory Molecular orbital theory is a theory of the electronic structure of molecules in terms of molecular orbitals, which may spread over several atoms or the entire molecule. As atoms approach each other and their atomic orbitals overlap, molecular orbitals are formed. In the quantum mechanical view, both a bonding and an antibonding molecular orbital are formed.
Molecular Orbital Theory c-chemistry/conjugation-diels-alder-mo- theory/molecular-orbital-theory/v/intro-to- molecular-orbital-mo-theoryhttps:// c-chemistry/conjugation-diels-alder-mo- theory/molecular-orbital-theory/v/intro-to- molecular-orbital-mo-theory
Molecular Orbital Theory For example, when two hydrogen atoms bond, a 1s (bonding) molecular orbital is formed as well as a 1s * (antibonding) molecular orbital. The following slide illustrates the relative energies of the molecular orbitals compared to the original atomic orbitals. Because the energy of the two electrons is lower than the energy of the individual atoms, the molecule is stable.
H atom H 2 molecule 1s 1s 1s *
Energy levels of bonding and antibonding molecular orbitals in hydrogen (H 2 ). A bonding molecular orbital has lower energy and greater stability than the atomic orbitals from which it was formed. An antibonding molecular orbital has higher energy and lower stability than the atomic orbitals from which it was formed.
Two Possible Interactions Between Two Equivalent p Orbitals
The arrows show the occupation of molecular orbitals by the valence electrons in N 2.
1.The number of molecular orbitals (MOs) formed is always equal to the number of atomic orbitals combined. 2.The more stable the bonding MO, the less stable the corresponding antibonding MO. 3.The filling of MOs proceeds from low to high energies. 4.Each MO can accommodate up to two electrons. 5.Use Hund’s rule when adding electrons to MOs of the same energy. 6.The number of electrons in the MOs is equal to the sum of all the electrons on the bonding atoms. Molecular Orbital (MO) Configurations
Sigma Bonding and Antibonding Orbitals Copyright © Cengage Learning. All rights reserved 58 To play movie you must be in Slide Show Mode PC Users: Please wait for content to load, then click to play Mac Users: CLICK HERECLICK HERE
Bond Order Larger bond order means greater bond strength. Copyright © Cengage Learning. All rights reserved 59
Example: H 2
Example: H 2 – Copyright © Cengage Learning. All rights reserved 61
Homonuclear Diatomic Molecules Composed of 2 identical atoms. Only the valence orbitals of the atoms contribute significantly to the molecular orbitals of a particular molecule. Copyright © Cengage Learning. All rights reserved 62
Pi Bonding and Antibonding Orbitals Copyright © Cengage Learning. All rights reserved 63 To play movie you must be in Slide Show Mode PC Users: Please wait for content to load, then click to play Mac Users: CLICK HERECLICK HERE
Paramagnetism Paramagnetism – substance is attracted into the inducing magnetic field. –Unpaired electrons (O 2 ) Diamagnetism – substance is repelled from the inducing magnetic field. –Paired electrons (N 2 ) Copyright © Cengage Learning. All rights reserved 64
Apparatus Used to Measure the Paramagneti sm of a Sample Copyright © Cengage Learning. All rights reserved 65
Molecular Orbital Summary of Second Row Diatomic Molecules Copyright © Cengage Learning. All rights reserved 66
Heteronuclear Diatomic Molecules Composed of 2 different atoms. Copyright © Cengage Learning. All rights reserved 67
Heteronuclear Diatomic Molecule: HF The 2p orbital of fluorine is at a lower energy than the 1s orbital of hydrogen because fluorine binds its valence electrons more tightly. –Electrons prefer to be closer to the fluorine atom. Thus the 2p electron on a free fluorine atom is at a lower energy than the 1s electron on a free hydrogen atom. Copyright © Cengage Learning. All rights reserved 68
Orbital Energy-Level Diagram for the HF Molecule Copyright © Cengage Learning. All rights reserved 69
Heteronuclear Diatomic Molecule: HF The diagram predicts that the HF molecule should be stable because both electrons are lowered in energy relative to their energy in the free hydrogen and fluorine atoms, which is the driving force for bond formation. Copyright © Cengage Learning. All rights reserved 70
The Electron Probability Distribution in the Bonding Molecular Orbital of the HF Molecule Copyright © Cengage Learning. All rights reserved 71
Heteronuclear Diatomic Molecule: HF The σ molecular orbital containing the bonding electron pair shows greater electron probability close to the fluorine. The electron pair is not shared equally. This causes the fluorine atom to have a slight excess of negative charge and leaves the hydrogen atom partially positive. This is exactly the bond polarity observed for HF. Copyright © Cengage Learning. All rights reserved 72
Delocalization Describes molecules that require resonance. In molecules that require resonance, it is the π bonding that is most clearly delocalized, the σ bonds are localized. p orbitals perpendicular to the plane of the molecule are used to form π molecular orbitals. The electrons in the π molecular orbitals are delocalized above and below the plane of the molecule. Copyright © Cengage Learning. All rights reserved 73
Resonance in Benzene Copyright © Cengage Learning. All rights reserved 74
The Sigma System for Benzene Copyright © Cengage Learning. All rights reserved 75
The Pi System for Benzene Copyright © Cengage Learning. All rights reserved 76
Delocalized molecular orbitals are not confined between two adjacent bonding atoms, but actually extend over three or more atoms.
Electron density above and below the plane of the benzene molecule.
Pi Bonding in the Nitrate Ion Copyright © Cengage Learning. All rights reserved 80 To play movie you must be in Slide Show Mode PC Users: Please wait for content to load, then click to play Mac Users: CLICK HERECLICK HERE
Copyright © Cengage Learning. All rights reserved 81 Can be used to determine the relative energies of electrons in individual atoms and molecules. High-energy photons are directed at the sample, and the kinetic energies of the ejected electrons are measured.