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Beckmann rearrangement
Ketoxime while treated with acid at 0°C it goes through rearrangement termed as Beckmann rearrangement.
So, acid catalysed conversion of ketoximes to N-substituted amides is known as Beckmann rearrangement. Acid catalyst utilized is proton acids (H2SO4, HCl, H3PO4) and Lewis acids (PCl5, SOCl2, PhSO2Cl, RCOCl, SO3, BF3 etc)
between nitrobenzene and phenol which is more reactive towards chlorine and why? Upon reaction with chlorine what products can be formed from the two reactions.
How coloured ion is formed
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