Beckmann rearrangement in benzophenone oxime, a mass spectrometric study
J. R. Majer, A.S.P. Azzouz
Abstract
J. R. Majer, A.S.P. Azzouz
Abstract
Abstract The isomerization of benzophenone oxime to benzanilide, previously observed to take place in the ion source of a mass spectrometer and attributed to a Beckmann type rearrangement of the benzophenone oxime molecule ion, has been shown to occur by a thermal mechanism prior to ionization. Mass spectrometric evidence is supplemented by infrared spectrophotometric examination of solid samples and shows that in the solid state, at room temperature, benzophenone oxime has a lifetime of about 600 h.
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Abstract The isomerization of benzophenone oxime to benzanilide, previously observed to take place in the ion source of a mass spectrometer and attributed to a Beckmann type rearrangement of the benzophenone oxime molecule ion, has been shown to occur by a thermal mechanism prior to ionization. Mass spectrometric evidence is supplemented by infrared spectrophotometric examination of solid samples and shows that in the solid state, at room temperature, benzophenone oxime has a lifetime of about 600 h.
Key concepts: Benzophenone, Oxime, Beckmann rearrangement, Chemistry, Mass spectrometry, Isomerization, Photochemistry, Molecule