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In page Phenol:
"The major uses of phenol, consuming two thirds of its production, involve its conversion to precursors for plastics. Condensation with acetone gives bisphenol-A, a key precursor to polycarbonates and epoxide resins. Condensation of phenol, alkylphenols[citation needed], or diphenols[citation needed] with formaldehyde gives phenolic resins, an example of which is Bakelite. Partial hydrogenation of phenol gives cyclohexanone,[1] a precursor to nylon. Nonionic detergents are produced by alkylation of phenol to give the alkylphenols, e.g., nonylphenol, which are then subjected to ethoxylation.[2]
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