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Molecular Structure

Molecular

Geometry

(VSEPR)

I II

III

YouTube

Video on VSPER Theory

Learning Objectives

 TLW predict molecular structure for molecules using Valence Shell Electron

Pair Repulsion (VSEPR) Theory (TEKS

7.E)

A. VSEPR Theory

1. V alence S hell E lectron P air R epulsion

Theory gives us a three-dimensional picture of atomic bonding that the

Electron Dot Structure does not.

2. Electron pairs orient themselves in order to minimize repulsive forces.

VSEPR:

3. Predicts three dimensional geometry of molecules.

4. The name tells you the theory:

5. Valence shell - outside electrons.

6. Electron Pair repulsion - electron pairs try to get as far away as possible.

7. Can determine the angles of bonds.

A. VSEPR Theory

Types of e Pairs

1. Bonding pairs - form bonds

2. Lone pairs - nonbonding e -

Lone pairs repel more strongly than bonding pairs!!!

A. VSEPR Theory

 Lone pairs reduce the bond angle between atoms.

Bond Angle

B. Determining Molecular Shape

1. Draw the Lewis Diagram.

2. Tally up e pairs on central atom.

a. double/triple bonds = ONE pair

3. Shape is determined by the # of bonding pairs and lone pairs.

Know the 3 most common shapes

& their bond angles!

C. Common Molecular Shapes 1

2 total

2 bond

0 lone

BeH

2

LINEAR

180 °

Examples

 CO

2

2 total

2 bond

0 lone

O C O

LINEAR

180 °

C. Common Molecular Shapes 2

3 total

2 bond

1 lone

SO

2 BENT

<120 °

C. Common Molecular Shapes 3

3 total

3 bond

0 lone

BF

3

TRIGONAL PLANAR

120 °

C. Common Molecular Shapes 4

4 total

4 bond

0 lone

CH

4

TETRAHEDRAL

109.5

°

C. Common Molecular Shapes 5

4 total

3 bond

1 lone

NH

3

TRIGONAL PYRAMIDAL

107 °

Examples

 PF

3

4 total

3 bond

1 lone

F P F

F

TRIGONAL

PYRAMIDAL

107 °

C. Common Molecular Shapes 6

4 total

2 bond

2 lone

H

2

O

BENT

104.5

°

C. Common Molecular Shapes 7

5 total

5 bond

0 lone

PCl

5

TRIGONAL

BIPYRAMIDAL

120 °/90°

C. Common Molecular Shapes 8

6 total

6 bond

0 lone

SF

6

OCTAHEDRAL

90 °

Examples

 linear: BeH

2

, CO

2

, MgF

2

, I

3 bent (angular): SO

2

, H

2

O, H square planar: XeF

4

, IF

4

-

2

S, SF

2 trigonal planar : SO

3

, BF

3 square pyramidal: IF

5

, BrF

5 trigonal pyramidal: NH

3

, PF

3

, AsCl

3 trigonal bipyramidal: PF

5

, PCl

5

, AsF tetrahedral : CH

4

, CF

4

, SO

4

2-

5 octahedral: SF

6

, PF

6

, SiF

6

2seesaw: SF

4

T-shaped: ClF

3

D. Orbital Hybridization

 VSEPR Theory works well when accounting for molecular shapes, but doesn’t help describing the types of bonds formed.

 In hybridization, several atomic orbitals mix to form the same total number of equivalent hybrid orbitals

 YouTube video

D. Orbital Hybridization

 For Example ~ Methane (CH

4

)

C = 1s 2 2s 2 2p 2

H = 1s 1 (and there are four H atoms)

C re-configures its one 2s and three 2p orbitals into four sp 3 orbitals, which overlap the 1s orbitals of the 4 hydrogen atoms

Group Practice

 Molecular Geometry Construction

Game Revisited

E. One Other Note on Bonding

 Electronegativity determines bonding which contributes to the bond angle

Greater than 1.7  ionic bonds

0.3 – 1.7  polar covalent bonds

0 – 0.3  covalent

See handout for trends through periodic table

Electronegativities

Greater than 1.7

 ionic bonds

0.3 – 1.7

 polar covalent bonds

0 – 0.3

 covalent

Independent Practice

 Building 3-D Examples of Molecular

Geometry

VSEPR Marshmellow Lab

 VSEPR Exercise – 2

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