In stereochemistry, mutarotation is the change in optical rotation of a chiral material in a solution due to a change in proportion of the two constituent anomers (i.e. the interconversion of their respective stereocenters) until equilibrium is reached. Cyclic sugars show mutarotation as α and β anomeric forms interconvert. The optical rotation of the solution depends on the optical rotation of each anomer and their ratio in the solution.
La mutarotazione è un fenomeno, osservato per la prima volta nel 1846, che consiste nel cambiamento di potere rotatorio osservato per alcuni carboidrati in soluzione.
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Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).