Lecture 30 |
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(Next moving to Chapter 19) |
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Lecture Outline |
Intermolecular Interactions
Oxidation Numbers |
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Some definitions relevant to discussions on solubility. | ||
What effects determine solubility? | ||
The dependence of the solubilities of different alcohols on their molecular structure | ||
Interpretation of alcohol solubilities in terms of molecular structure and intermolecular interactions | ||
Another comparison to make. | ||
Vitamin A shown here is essentially a nonpolar molecule. It is very polarizable because of its "size" (and also because pi electrons are very polarizable, a detail we haven't worried about and will not). Consequently, it is not very soluble in water but quite soluble in a nonpolar solvent such as "fat" (which is mostly hydrocarbon-like in nature). | ||
In contrast to Vitamin A, you can see here from the structure of Vitamin C that extensive hydrogen bonding with solvent water molecules should be possible, explaining why it is a water soluble vitamin. | ||
Acetic acid, as a small, polar molecule capable of hydrogen bonding with water is very soluble in water. You might reasonably expect it to be insolube in nonpolar solvents. However, a subtle phenomenon causes acetic acid to be soluble in nonpolar solvents as well. See below. | ||
Acetic acid can effectively "dimerize", form a double structure held togeter very effectively by a geometrical arrangement that accommodates double hydrogen bonding. The resulting structure has no dipole moment. The "dimer" can then serve as a solvent in nonpolar solvents. | ||
Our rules for oxidation numbers. These are "heirarchical", that is, each rule's rank determines their importance relative to other rules. They are not the same as in Table 4.3. | ||
Oxidation number rules continued | ||
Oxidation number rules continued |