VSEPR Theory VSEPR Theory Shapes of

 Molecular Structure or  The 3-dimensional arrangement of the atoms that make-up a .  Determines several properties of a substance, including: reactivity, polarity, phase of matter, color, magnetism, and biological activity.  The chemical formula has no direct relationship with the shape of the molecule. VSEPR Theory Shapes of Molecules

 Molecular Structure or Molecular Geometry  The 3-dimensional shapes of molecules can be predicted by their Lewis structures.  -shell electron pair repulsion (VSEPR) model or electron domain (ED) model:  Used in predicting the shapes.  The electron pairs occupy a certain domain.  They move as far apart as possible.  Lone pairs occupy additional domains, contributing significantly to the repulsion and shape. VSEPR Theory Terms and Definitions

 Bonding Pairs (AX) Electron pairs that are involved in the bonding.  Lone Pairs (E) – aka non-bonding pairs or unshared pairs Electrons that are not involved in the bonding. They tend to occupy a larger domain.  Electron Domains (ED) Total number of pairs found in the molecule that contribute to its shape. VSEPR – Molecular Shape

 Multiple covalent bonds  Bond Angle: around the same atom • Angle formed by any determine the shape two terminal (outside)  Negative e- pairs (same atoms and a central charge) repel each other atom • Caused by the repulsion  Repulsions push the pairs as far apart as possible of shared electron pairs. Hybridization

 What’s a hybrid? • Combining two of the same type of object and contains characteristics of both • Occurs to orbitals during bonding  Orbital hybridization • Process in which atomic orbitals are mixed to form new hybrid orbitals • Each hybrid orbital contains one electron that it can share with another atom  Carbon is most common atom to undergo hybridization • Four hybrid orbitals from 1 s and 3 p orbitals • Hybrid = sp3 orbital Orbital Hybridization

 Atomic orbitals such as s and p are not well suited for overlapping and allowing two atoms to share a pair of electrons  The best location of shared pair is directly between two atoms  e- pair spends little time in best location • With overlap of two s-orbital • With overlap of two p-orbitals Orbital Hybridization

 Hybrid orbitals (cross of atomic orbitals) •Shape more suitable for bonding  One large lobe and one very small lobe  Large lobe oriented towards other nucleus •Angles more suitable for bonding  Angles predicted from VSEPR Orbital Hybridization Overlap of two s-orbitals Note: shared in this overlap the e- pair would spend most of the time in an unfavorable location

GOOD SPOT between both nuclei

NOT A GOOD LOCATION- Too far from one nucleus Orbital Hybridization

Overlap of two p-orbitals

GOOD SPOT BAD location far from BAD location far from other nucleus between both other nucleus nuclei One atom & its The other atom & p-orbital its p-orbital

represents the nucleus Orbital Hybridization

 Hybrid orbitals yield more favorable shape for overlap • Atomic orbitals are not shaped to maximize attractions nor minimize repulsions  Hybrid orbital shape • One large lobe oriented towards other atom • Notice the difference in this shape compared to p-orbital shape Orbital Hybridization

 Hybrid orbitals create more favorable angles for overlap, too. Atomic orbitals are not shaped to maximize attractions nor minimize repulsions  BUT the angles are also not favorable p-orbitals are oriented at 90 to each other Other angles are required:  180, 120, or 109.5  Orbital Hybridization

-  Each e pair requires a hybrid orbital  If two hybrid orbitals required than two atomic orbitals must be hybridized, an s and a p orbital forming two sp orbitals at 180

sp hybrids sp2 hybrids sp3 hybrids

2 EP 3 EP 4 EP sp-Hybridization sp2 -Hybridization sp3 -Hybridization Hybridization – Key Points

 The number of hybrid (molecular) orbitals obtained equals the number of atomic orbitals combined.  The type of hybrid orbitals obtained varies with the types of atomic orbitals mixed.  Examples: • 1 s + 1 p = 2 sp orbitals • 1 s + 2 p = 3 sp2 orbitals • 1 s + 3 p = 4 sp3 orbitals Electron-Pair Geometry vs Molecular Geometry

 Electron-pair geometry • Where are the electron pairs • Includes  bonding pairs (BP) = shared between 2 atoms  nonbonding pairs (NBP) =  Molecular geometry • Where are the atoms • Includes only the bonding pairs

2 Electron Domains (ED) around central atom

 Two clouds pushed as far apart as possible • Greatest angle possible 180 • LINEAR shape

Linear

 Bonding Pairs: 2

 Lone Pairs: 0

 Electron Domains: 2

 Bond Angle: 180°

 Example: CO2 Image: Linear

Carbon Dioxide (CO2)

Nitrogen Gas (N2) 3 Electron Domains (ED) around central atom

 Three electron clouds pushed as far apart as possible • Greatest angle possible = 120 • TRIGONAL (3) PLANAR (flat) shape

Examples of 3 ED

 3 Bonded Pairs + 0 Non-Bonded Pairs • 3 ED = Electron Pair Geometry is trigonal planar • All locations occupied by atoms, • So Molecular Geometry is also trigonal planar  2 Bonded Pairs + 1 Non-Bonded Pair • 3 ED = Electron Pair Geometry is trigonal planar • Only two bonding pairs • One of the locations is only lone pair of e- • So molecular geometry is bent Trigonal Planar

 Bonding Pairs: 3

 Lone Pairs: 0

 Electron Domains: 3

 Bond Angle: 120°

 Example: BF3 Image: Trigonal Planar

2- Ion (CO3 )

- Nitrate Ion (NO3 ) Bent or Angular

 Bonding Pairs: 2

 Lone Pairs: 1

 Electron Domains: 3

 Bond Angle: 120° (119°)

 Example: SO2 Image: Bent or Angular

- Nitrite Ion (NO2 ) 4 Electron Domains (ED) around central atom

 Four clouds pushed as far apart as possible • Greatest angle no longer possible in two dimensions • Requires three-dimensional • TETRAHEDRAL shape Examples of 4 ED

 4 Bonded Pairs + 0 Non-Bonded Pairs • 4 ED:  Both Electron Pair Geometry and Molecular Geometry are tetrahedral  3 Bonded Pairs + 1 Non-Bonded Pair • 4 ED:  Electron Pair Geometry is tetrahedral  Molecular Geometry is TRIGONAL PYRAMIDAL  No atom at top location  2 Bonded Pairs + 2 Non-Bonded Pairs • 4 ED:  Electron Pair Geometry is tetrahedral  Molecular geometry is BENT  No atoms at two locations Tetrahedral

 Bonding Pairs: 4

 Lone Pairs: 0

 Electron Domains: 4

 Bond Angle: 109.5°

 Example: CH4 Image: Tetrahedral

Silicon Tetrachloride (SiCl4)

Methane (CH4) Trigonal Pyramidal

 Bonding Pairs: 3

 Lone Pairs: 1

 Electron Domains: 4

 Bond Angle: 109.5° (107.5°)

 Example: NH3 Image: Trigonal Pyramidal

+ Hydronium Ion (H3O )

Ammonia (NH3) Bent or Angular (Ver. 2)

 Bonding Pairs: 2

 Lone Pairs: 2

 Electron Domains: 4

 Bond Angle: 109.5° (104.5°)

 Example: H2O Image: Bent or Angular (Ver. 2)

Chlorine Difluoride (ClF2) Summary of 4 Electron Domain Shapes Exceptions to Octet Rule

 Reduced Octet • H only forms one bond  only one pair of e- • Be tends to only form two bonds  only two pair of e- • B tends to only form three bonds  only three pair of e-  Expanded Octet • Empty d-orbitals can be used to accommodate extra e- • Elements in the third row and lower can expand • Up to 6 pairs of e- are possible Lewis Structures in Which the Central Atom Exceeds an Octet Summary: Molecular Geometry of Expanded Octets