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SUMMARY The bleaching of anthocyanins by sulfur dioxide is a reversible process that does not involve hydrolysis of the 3‐glycosidic group, reduction of the pigment, or addition of bisulfite to a ketonie, chalcone derivative. In sulfite decoloration the reactive species is the anthocyanin carbonium ion (R + ). The experimental evidence indicates that this simply reacts with a bisulfite ion to form a colorless chromen‐2 (or 4)‐sulfonic acid (R‐SO 3 H), similar in structure and properties to an anthocyanin carbinol base (R‐OH).
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Leonard Jurd (1964) studied this question.
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