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The reaction of phenyl magnesium bromide and benzophenone was quenched with sulfuric acid, and an extraction was performed in order to separate the organic phase containing the triphenylmethanol from the aqueous phase. The triphenlmethanol was then isolated and purified by crystallization and vacuum filtration.
Reaction Scheme:
Mechanism: The nucleophilic phenyl magnesium bromide attacks the electrophilic carbonyl of benzophenone to form a magnesium alkoxide. This is followed by hydrolysis by an acid to produce the alcohol, triphenylmethanol.
Procedure: The procedure followed was as is described in "Laboratory Manual for Organic Chemistry 2311," Fifth Edition, Jane E...
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Common topics in this essay:
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