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Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

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Page 1: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

Hybridization ofAtomic Orbitals

Some Material Copyright PGCC CHM 101 SinexSome Graphics from Nelson Chemistry 12

Textbook

Page 2: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

Atomic Orbitals Don’t Work?

To explain molecular geometry:

• In methane, CH4 , the shape is tetrahedral.

• The valence electrons of carbon should be two in s, and two in p.

• The p orbitals would have to be at right angles.

• The atomic orbitals change when making a molecule

Page 3: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

Valence Bond Theory

• Atomic orbitals overlap when a bond is formed between atoms

• A new set of orbitals is formed • Each orbital contains a pair of

electrons• These are called hybrid orbitals• How do they look? See p234 Table 1

Page 4: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

Hybridization

• p234 Table 1Ex: sp3 hybridization

Page 5: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

sp3 Hybridization

• The s and p orbitals blend and end up with the tetrahedral geometry.

• one s orbital combines with three p orbitals.

• sp3 hybridization has tetrahedral geometry.

Page 6: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

2p

Hybridization sp3

2s

Energy

In Terms of Energy

Page 7: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

Notation?

sp3

•One s orbital and three p orbitals•Each orbital holds 2 electrons

Page 8: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

Illustrating Hybridization

Animation of hybridizationhybridization

Visualization of orbitalshybrid orbitals

Page 9: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

Double and Triple Bonds

Ex: C2H4

• Double bond acts as one pair.• Geometry - trigonal planar• Have to end up with three blended

orbitals.• Use one s and two p orbitals to make

sp2 orbitals.• Leaves one p orbital perpendicular.

Page 10: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

Where is the P orbital?

• Perpendicular• The overlap of orbitals (end-to-end)

makes a sigma bond ( bond)

Page 11: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

hybrid orbitals – sp, sp2, or sp3

Page 12: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook
Page 13: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook
Page 14: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

formation of bond

Page 15: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

remaining p orbitals form sp or sp2

bond

Page 16: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook
Page 17: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook
Page 18: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

The overlap of orbitals (side-to-side)

makes a pi bond ( bond)

Planar molecule (each carbon is trigonal planar) with cloud above and below the plane

bond hinders rotation about the carbon-to-carbon bond

Page 19: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

sp Hybridization

• End up with two lobes 180º apart.• p orbitals are at right angles• Makes room for two bonds and

two bonds.• A triple bond or two double

bonds.

Page 20: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

Bond Formation From Hybridization

• Single bond - sigma bond

• Double bond – sigma bond + pi bond

• Triple bond – sigma bond + pi bond + pi

bond How are the two pi bonds in the triple bond oriented?

end-to-end

side-to-side

Page 21: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

How about the electron density around a C-C bond?

C2H6

C2H4C2H2

single bond double bond triple bond

Polar orNon-polar

H+

attack?

Page 22: Hybridization of Atomic Orbitals Some Material Copyright PGCC CHM 101 Sinex Some Graphics from Nelson Chemistry 12 Textbook

Summary