what is phenolic bromine astoes
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Reaction with bromine water
If bromine water is added to a solution of phenol in water, the bromine water is decolourised and a white precipitate is formed which smells of antiseptic. Notice the multiple substitution around the ring - into all the activated positions.
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In the present study, carbon and bromine isotope effects during UV-photodegradation of bromophenols in aqueous and ethanolic solutions were determined. An anomalous relatively high inverse bromine isotope fractionation (εeactive position up to +5.1%) along with normal carbon isotope effect (reactive position of -12.6% to -23.4%) observed in our study may be attributed to coexistence of both mass-dependent and mass-independent isotope fractionation of C-Br bond cleavage. Isotope effects of a similar scale were observed for all the studied reactions in ethanol, and for 4-bromophenol in aqueous solution. This may point out related radical mechanism for these processes. The lack of any carbon and bromine isotope effects during photodegradation of 2-bromophenol in aqueous solution possibly indicates that C-Br bond cleavage is not a rate-limiting step in the reaction. The bromine isotope fractionation, without any detectable carbon isotope effect, that was observed for 3-bromophenol photolysis in aqueous solution probably originates from mass-independent fractionation.
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