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Within the alkane, alkene and alkyne families certain trends appear. For example: at the low end methane, ethane, propane, ethene and ethyne are all gases at room temperature. The slightly larger molecules are liquids, then waxy solids. Because they are covalent molecules, they never get very strong, as one molecule is always rather easily parted from another. A candle is a typical mixed longer-chain alkane. Petrol is a typical mixed medium-chain alkane. The gas you burn in a Bunsen burner is a typical mixed short-chain alkane, although it is predominantly methane. We are still short of being able to build even the simplest living cell.
Table 2. Melting and boiling point for first ten alkanes. (Alyward & Findlay, SI Chemical Data, Wiley & Sons.) Thus you can draw a generalisation that longer chains have higher melting and boiling points than shorter ones. Similarly, straight chains lead to higher melting points than branched molecules with similar numbers of carbons. That is, you would expect hexane to have a higher melting point than dimethylbutane, even though both are of the formula C6H14, as indicated in Table 3 below. This last observation leads very handily into the next topic.
Table 3. Melting and boiling point for four alkanes with the formula C6H14. (Alyward & Findlay, SI Chemical Data, Wiley & Sons.) Problem 6. From your recollection of bonding and intermolecular forces, suggest an explanation for this generalisation.
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