7 Carbohydrates 237
CH 2 OHH OHHO HH OHH OHCH 2 OH
GlucitolCH 2 OHHO HHO HH OHH OHCH 2 OH
MannitolCH 2 OHOHO HH OHH OHCH 2 OHReductionFructoseFig. 7.8Glucitol and mannitol produced after reduction of fructose
Reducing power of sugars is the basis of a number of classical analytical methods.
Iodine, alkaline ferricyanide and other reagents have been used for analytical pur-
poses.
- Glycoside formation: hemiacetals react with alcohols to form acetals, called gly-
cosides. Acetal formation locks the ring structure, preventing oxidation-reduction
and mutarotation reactions. When acarbonyl group reacts with a hydroxyl group
from other sugar molecule, a disaccharide is created: the formed acetal is sta-
ble and it is called “glycosidic linkage”. Monosaccharides can be polymerized
through glycosidic linkages to form disaccharides, trisaccharides and polysac-
charides.