Chapter Molecules are 3D. Shapes and Bonds. Chapter 9 1. Chemical Bonding and Molecular Structure

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Chapter 9 Chemical Bonding and Molecular Structure 1 Shape 9.1 Molecules are 3D Angle Linear 180 Planar triangular (trigonal planar) 120 Tetrahedral 109.5 2 Shapes and Bonds Imagine a molecule where the central atom is the Earth. Equatorial bonds bonds located around the equator Axial bonds bonds pointing along the north and south axis of the central atom. 3 Chapter 9 1

9.1 Molecular Shapes Continued Shape Angle Trigonal bipyramidal 120 and 90 Octahedral 90 4 9.2 Molecular shapes are predicted using the VSEPR model You have seen the 5 basic molecular shapes. Notice, they assume that the central atom is surrounded only by atoms. What if there are electron pairs on the central atom? How do they affect the molecular shape? 5 VSEPR Model Valence Shell Electron-Pair Repulsion Model Electrons pairs in the outer shell of an atom try to get as far away from each other as possible Why? Because like charges repel they want to be far away from each other. 6 Chapter 9 2

Domains Electron domain a region of space where electrons can be found Bonding domains electron pairs that are involved in bonds between two atoms, doesn t matter if it is a single, double or triple bond. Nonbonding domains valence electrons that are associated with a single atom. Electron domains keep as far away as possible from each other. 7 Geometry and Domains Let s look at BeCl 2 and SnCl 2 What are their Lewis Structures? When we draw them, we will tend to draw them linear. Does this mean they have linear geometry? NO! 8 BeCl 2 is linear. SnCl 2 is bent. We can use what we know about bonding and nonbonding domains to predict the molecular shape. If a molecule has nonbonding domains, the shape will deviate from the 5 basic shapes. Consider the handout on VSEPR structures. Let s look at all the molecules we drew in Chapter 8 and determine their molecular shape. 9 Chapter 9 3

9.3 Molecular symmetry affects the polarity of molecules Remember polar bonds? Polar bonds can result in a polar molecule, depending on the geometry of the molecule. To determine polarity: Draw Lewis Structure Determine the Molecular Geometry See if you move 10 Nonpolar Molecules Polar Molecules Let s go back to those molecules from Chapter 8 and determine if they are polar or nonpolar. 11 9.4 Valence Bond Theory A bond between two atoms is formed when a pair of electrons with their spins paired is shared by two overlapping atomic orbitals, one orbital from each of the atoms joined by the bond. WHAT! 12 Chapter 9 4

Atoms tend to position themselves so the the maximum amount of orbital overlap occurs This yields the minimum potential energy and the strongest bonds. 13 H 2 S How does VB balance with bond angles? What orbitals in S will overlap with the 1s orbitals of the hydrogen atoms? Note: two orbitals from different atoms never overlap simultaneously with opposite ends of the same p-orbital. 14 There is a clear problem! The geometry of the p-orbitals dictates an angle of 90. What was the experimental angle of H 2 S? How can this be explained? 15 Chapter 9 5

9.5 Hybrid Orbitals Think back to sixth grade biology. Remember Mendel? He made hybrids of pea plants by mixing purebreds. We will apply a similar method to atomic orbitals (s, p, d). Atomic orbitals can be hybridized to generate a new set of directional orbitals. These mixed orbitals match the orbital geometry of the compounds. Remember, all electrons around the central atom must be in orbitals --- whether they are nonbonding electrons or bonding electrons. What do they look like? 16 Mixing the 2s and (one) 2p atomic orbital results in a pair of sp hybrid orbitals. Note that the large lobes of these hybrid orbitals point in opposite directions. 17 When an s orbital combines with two p orbitals, three sp 2 hybrid orbitals are formed. When an s orbital combines with three p orbitals, four sp 3 hybrid orbitals are formed. When an s orbital combines with three p orbitals and a d orbital, five sp 3 d hybrid orbitals are formed. When an s orbital combines with three p orbitals and two d orbitals, six sp 3 d 2 hybrid orbitals are formed. The number of orbitals is conserved: the number of hybrid orbitals in a set equals the number of atomic orbitals used to form the set. 18 Chapter 9 6

Atomic orbitals that contribute to hybridization # of hybrid orbitals Hybrid orbitals formed Orbitals left over (usually participate in double/triple bonds) 2 3 4 none s+ p x + p y + p z + d 5 sp 3 d none s+ p x + p y + p z + d + d 6 sp 3 d 2 none 19 20 21 Chapter 9 7

Molecules with nonbonding domains can also be described with hybrid orbitals Lone pairs occupy a bit more volume than bonding electron pairs NH 3 is tetrahedral and should have a bond angle of 109.5. Experimentally, it has a bond angle of 107º. This is due to the lone pair electrons. Remember the VSEPR Model. A similar phenomena is seen in H 2 O, but oxygen has two lone pairs of electrons resulting in an angle of 104.5º. Let s go back to the molecules from Chapter 8 and determine the hybridization. 22 9.6 Hybrid Orbitals and Multiple Bonds There are two types of bonds that comprise single, double and triple bonds. Sigma bond (σ) when electron density is between the nuclei of the two atoms Pi bond (π) when electron density is divided between two separate regions. 23 σ bonds 24 Chapter 9 8

π bonds 25 Multiple Bonds Multiple bonds almost always consist of a single sigma bond and one or more pi bonds The pi bonds are formed from the p orbitals that are not involved in the hybrid orbitals. What is the hybridization of the carbons in ethene? 26 Ethene Hybridization The carbons have 3 bonding domains. Therefore, they are each sp 2 hybridized. To make the sp 2 hybrid orbitals, one s orbital and two p orbitals were mixed. What is left over? 27 Chapter 9 9

28 The sp 2 hybrid orbitals overlap to form a sigma bond. Where does the double bond come from? 29 The p-orbitals on each carbon that is left over (after hybridization) will form a π overlap. A double bond consists of a sigma and a pi overlap (σ + π) 30 Chapter 9 10

Bonds and Rotation Groups connected by single bonds can freely rotate Rotation is restricted around double bonds. The overlap for the pi bond would be lost. 31 Triple Bonds Let s examine acetylene (H-C C-H) What is the hybridization of the carbons? 32 The sp hybrid orbital is formed from one s and one p orbital. There are still two p orbitals left. 33 Chapter 9 11

A triple bonds results from a sigma bond and two pi bonds (σ + π + π). 34 VB Theory Summary 1. The basic framework of the molecule is determined by the arrangement of its sigma-bonds 2. Hybrid orbitals are used by an atom to form its sigmabonds and to hold the lone pairs of electrons. 3. The number of hybrid orbitals needed by an atom in a structure equals the number of atoms to which it is bonded plus the number of lone pairs of electrons in its valence shell. 4. When there is a double bond in a molecule, it consists of one sigma and one pi bond 5. When there is a triple bond, it consists of one sigma and two pi bonds 35 Chapter 9 12