Robert Filler, Frank P. Avonda
Abstract
Decafluorobenzhydryl bromide (1) reacts with nucleophiles to give 1,1,2,2-tetrakis(pentafluorophenyl)-ethane (2) as the predominant product; there is no evidence of products derived from initial nucleophilic displacement on the carbon of (1).
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Decafluorobenzhydryl bromide (1) reacts with nucleophiles to give 1,1,2,2-tetrakis(pentafluorophenyl)-ethane (2) as the predominant product; there is no evidence of products derived from initial nucleophilic displacement on the carbon of (1).
Key concepts: Nucleophile, Bromide, Chemistry, Character (mathematics), Displacement (psychology), Medicinal chemistry, Carbon fibers, Product (mathematics)