How bonds break, and the free radicals, carbocations and carbanions that result. The inductive effect, resonance, the electromeric effect and hyperconjugation, and the types of organic reaction.
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A covalent bond can break evenly, so each atom keeps one electron, or unevenly, so one atom takes both. These are homolytic and heterolytic fission. They give free radicals, carbocations and carbanions: short-lived pieces, called reaction intermediates, that decide how a reaction goes. Alkyl groups make a carbocation more stable and a carbanion less stable.
Electrons are not fixed in a molecule. The inductive effect, a pull along single bonds, fades with distance. Resonance spreads electrons over several atoms and makes the hybrid more stable than any one structure. The electromeric effect is a temporary shift of a pi pair. Hyperconjugation spreads the electrons of a C-H bond into a neighbouring orbital.
A nucleophile is an electron-rich reagent that gives a pair of electrons. An electrophile is electron-poor and takes a pair. Organic reactions fall into four types: substitution, addition, elimination and rearrangement. You can often tell which one by counting how many molecules go in, how many come out, and what happens to the pi bonds.
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