WebAddition of acid or base destroys the bisulfite ion in equilibrium with the addition product, and regenerates the carbonyl compound. [Pg.639] From a theoretical point of view this is an extremely interesting reaction. WebAddition of acid or base destroys the bisulfite ion in equilibrium with the addition product, and regenerates the carbonyl compound. [Pg.639] From a theoretical point of view this is …
Bisulfite Sigma-Aldrich
WebPublisher Summary. This chapter summarizes the current knowledge of sugar-bisulfite addition compounds in the studies of general problem of browning. It suggests and discusses three modes of action to explain the inhibition of non-enzymatic browning by sulfur dioxide: the “antioxidant theory”, the “addition compound theory’’, and the ... WebBisulfite addition products are formed from aldehydes, methyl ketones, cyclic ketones (generally seven-membered and smaller rings), a- keto esters, and isocyanates, upon treatment with sodium bisulfite. Most other ketones do not undergo the reaction, probably for steric reasons. The reaction is reversible (by treatment of the addition product ... chip roux
Bisulfite addition products of ketone-terminated polyoxyalkylene ...
WebThe sulfur in the bisulfite ion acts as a nucleophile and adds to the carbonyl carbon. Because this is such ... bisulfite bisulfite addition complex. Aldehydes react with Schiff's reagent to produce a color change (magenta-colored addition product). In the same way, the Schiff reagent acts as a nucleophile that adds to the carbonyl group of an ... WebThe bisulfite addition products of this invention are also useful for preparing aqueous surfactant compositions in concentrations ranging from about 0.01 weight percent and … Web3) Recovering the ketone. Add the ~.25moles of bisulfite addition product to a separatory funnel then slowly pour in 105mL of 10% Sodium Hydroxide solution (w/w). Separate out … chip ross park