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PCC is Pyridinium ChloroChromate (Pyridinium chlorochromate). It oxidizes primary [alcohols] to aldehydes and secondary [alcohols] to ketones. One has to be careful with the amount of water present in the reaction. If water is present, it can add to the aldehyde to create the hydrate, which could be further oxidized by a second [equivalent] of PCC if it is present. This is not a concern with ketones because there is no H directly bonded to C
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