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Many of the most important chemical fuels are
compounds composed entirely of carbon and hydrogen,
In most other cases, it is not so trivial to determine which atoms are bonded to which, as there may be multiplepossibilities which satisfy all atomic valences. Nor is it trivial, as the number of atoms and electrons increases, to determinewhether each atom has an octet of electrons in its valence shell. We need a system of electron accounting which permits us to seethese features more clearly. To this end, we adopt a standard notation for each atom which displays the number of valenceelectrons in the unbonded atom explicitly. In this notation, carbon and hydrogen look like , representing the single valence electron in hydrogen and the four valence electrons in carbon.
Using this notation, it is now relatively easy to represent the shared electron pairs and the carbon atom valenceshell octets in methane and ethane. Linking bonded atoms together and pairing the valence shell electrons from each gives .
Recall that each shared pair of electrons
represents a chemical bond. These are examples of what are called
Lewis structures , after G.N. Lewis who first invented
this notation. These structures reveal, at a glance, which atomsare bonded to which,
In a larger hydrocarbon, the structural formula of the molecule is generally not predictable from thenumber of carbon atoms and the number of hydrogen atoms, so the molecular structure must be given to deduce the Lewis structure andthus the arrangement of the electrons in the molecule. However, once given this information, it is straightforward to create aLewis structure for molecules with the general molecular formula such as propane, butane, etc. For example, the Lewis structure for "normal" butane (with all carbons linked one afteranother) is found here .
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