Lecture #16 | ||
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Lecture Outline | Molecular Geometries
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The relative effectiveness of different electron pair repulsion combinations. The example illustrated shows how the HOH bond angle is distorted down to 104.5o from its ideal tetrahedral angle of 109.5o | ||
An illustration of how the differences between electron pair repulsions leading to the preferred see-saw geometry of a molecule of type AB4E. | ||
Further distortions from the ideal VSEPR geometry of a molecule of type AB4E. | ||
Here is the rationale behind choosing the T-shaped molecular geometry for two lone pairs and three bonding pairs about a central atom. (This was not done in lecture). Two of the choices have six unfavorable repulsions at 90o. The other has only four such repulsions. See it? | ||
Illustrating the imbalance when SF4's lone pairs distort bond angles and bond lengths from the ideal VSEPR geomtry. | ||
In a molecule of type AB4E2, the lone pair repulsions make the preferred molecular geometry that corresponding to square planar. This gives minimum lone pair-lone pair repulsions | ||
The molecular geometry of structure AB5E and the distortions from the ideal square pyramidal molecular geometry caused by the lone pair of electrons. | ||
Additional considerations that lead to distortions from ideal VSEPR molecular geometries. (These are not in the textbook.) | ||
Effect of multiple bonds. | ||
Illustration of double bond effect in POCl3 | ||
The effect of a lone single electron. | ||
Illustrating the lone electron effect by comparing ClO2- to ClO2 |