Epimers are pair of diasteroisomeric aldoeses which differ only in configuration at position:

Mutarotation is the change in specific rotation of an optically active compound in solution with time to an equilibrium value. Interconversion is possible only if sugar has anomeric hydroxyl group i.e., sugar is reducing. Diastereomers which differ in configuration of chiral carbon developed in hemiacetal formation are called anomers. Epimers are a pair of stereoisomers which differ in the configuration about one of its chiral carbon The anomeric carbon in fructose is

Mutarotation is the change in specific rotation of an optically active compound in solution with time to an equilibrium value. Interconversion is possible only if sugar has anomeric hydroxyl group i.e., sugar is reducing. Diastereomers which differ in configuration of chiral carbon developed in hemiacetal formation are called anomers. Epimers are a pair of stereoisomers which differ in the configuration about one of its chiral carbon On which carbon atom glucose and galactose differ in the position of -H and -OH groups?

Mutarotation is the change in specific rotation of an optically active compound in solution with time to an equilibrium value. Interconversion is possible only if sugar has anomeric hydroxyl group i.e., sugar is reducing. Diastereomers which differ in configuration of chiral carbon developed in hemiacetal formation are called anomers. Epimers are a pair of stereoisomers which differ in the configuration about one of its chiral carbon alpha- glucose and beta- glucose differ in configuration at ______ and are called

Anomers are those stereoisomers which differ in the configuration at

Glucose and galactose differ in configuration at:

A pair of diastereomers that differ only in the configuration about a single carbon atom are called