1 VSEPR Theory In any molecule or ion there are regions of high electron density: Bonds (shared electron pairs) Lone pairs (unshared electrons) Due to.

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Presentation transcript:

1 VSEPR Theory In any molecule or ion there are regions of high electron density: Bonds (shared electron pairs) Lone pairs (unshared electrons) Due to electron-electron repulsion, these regions are arranged as far apart as possible Such arrangement results in the minimum energy for the system

2 Five Basic Geometries Linear Trigonal Octahedral Trigonal bipyramidal Tetrahedral

3 CH 4, NH 3, and H 2 O  These molecules have the same electronic geometry but different molecular geometry

4  Electronic geometry  Distribution of regions of high electron density around the central atom  Molecular geometry  Arrangement of atoms around the central atom  If a molecule does not have lone electron pairs, both geometries are the same  If lone pairs are present, molecular and electronic geometries are different Electronic Geometry and Molecular Geometry

5 BeH 2 and H 2 O

6  Nonpolar Molecule  Dipole moments for all bonds cancel out  Polar Molecule  Dipole moments for all bonds don’t cancel out – the molecule has the resulting net dipole moment Polar and Nonpolar Molecules

7 BBr 3 and SO 2

8 Bond angles in CH 4, NH 3, H 2 O  VSEPR theory:  A lone pair takes up more space than a bond CH 4 NH 3 H2OH2O 109.5°107.3°104.5°

9 Polarity of CH 4, NH 3, H 2 O  Red – more electron density (more negative)  Blue – less electron density (more positive) CH 4 NH 3 H2OH2O

10 Bond angles in NH 3 and NF 3  More electronegative atoms pull electron density away from the central atom  The region around the central atom becomes less crowded and the bond angles decrease NH 3 NF °102.1°

11 PF 5, SF 4, ClF 3, and XeF 2

12 PF 5, SF 4, ClF 3, and XeF 2

13 The Lone Pair in SF 4 or F F F F F F F F S S 3 bonds at 90° 1 bond at 180° 2 bonds at 90° 2 bonds at 120°  There are 2 different positions in the trigonal bipyramid: axial and equatorial  Where does the lone pair go first?

14 SF 4 : Seesaw Shape

15 ClF 3 and XeF 2 ClF 3 XeF 2  In these molecules the 2nd and 3rd lone pairs still prefer to occupy the equatorial sites  In this way, the lone pairs are arranged farther apart from each other T-shapedLinear

16 TBP Electronic Geometry If lone pairs are incorporated into the trigonal bipyramidal structure, they occupy equatorial positions There are 3 possible shapes:  1 lone pair - Seesaw shape  2 lone pairs - T-shape  3 lone pairs – Linear

17 SeF 6, IF 5, and XeF 4

18 SeF 6 : Octahedron All bond angles are 90°

19 IF 5 and XeF 4 IF 5 XeF 4 Square Pyramidal Square Planar  The 1st lone pair can occupy any site  The 2nd lone pair is arranged opposite to the 1st

20 Octahedral Electronic Geometry If lone pairs are incorporated into the octahedral structure, there are 2 possible new shapes  1 lone pair – Square pyramid  2 lone pairs – Square planar

21 Assignments & Reminders Go through the lecture notes Read Chapter 8 completely Homework #5 covers Chapters 7 & 8 and is due by Oct. 31 Monday (10/24) and Tuesday (10/25) – lab quiz #2 (Experiments A, #5 & #9)