The Chemistry of Isopropyl

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hanlin
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The Chemistry of Isopropyl

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Unlike ethanol or methanol, isopropyl alcohol can be separated from aqueous solutions by adding a salt such as sodium chloride, sodium sulfate, or any of several other inorganic salts, since the alcohol is much less soluble in saline solutions than in salt-free water[6] The process is colloquially called salting out, and causes concentrated isopropyl alcohol to separate into a distinct layer.
Being a secondary alcohol, isopropyl alcohol can be oxidized to acetone, which is the corresponding ketone. This can be achieved using oxidizing agents such as chromic acid, or by dehydrogenation of isopropyl alcohol over a heated copper catalyst:
(CH3)2CH-OH → (CH3)2CO + H2
Isopropyl alcohol may be converted to 2-bromopropane using phosphorus tribromide, or dehydrated to propene by heating with sulfuric acid.
Isopropyl alcohol is often used as both solvent and hydride source in the Meerwein-Ponndorf-Verley reduction.
Like most alcohols, isopropyl alcohol reacts with active metals such as potassium to form alkoxides which can be called isopropoxides. The reaction with aluminium (initiated by a trace of mercury) is used to prepare the catalyst aluminium isopropoxide.
Isopropyl alcohol has a maximum absorbance at 204 nm in an ultraviolet-visible spectrum.
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