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D-glucitol
An alditol formed from the reduction of D-glucose; would it be optically active?
Alditols
Sugar alcohols formed via the reduction of monosaccharides.
Optically inactive alditols
The result of reduction of certain D-aldohexoses.
Phenylosazone
Product of the reaction of monosaccharides with phenylhydrazine.
Epimers
Stereoisomers that differ at one specific carbon atom.
Ruff Degradation
An oxidative decarboxylation process that reduces carbon chain length by one carbon.
Kiliani-Fischer Synthesis
A method for lengthening carbon chains in sugars, producing epimers.
Homopolysaccharides
Polymers consisting of a single type of monosaccharide.
Heteropolysaccharides
Polymers made up of more than one type of monosaccharide building block.
Cellulose
A structural polysaccharide found in plants, composed of β-glucose units.
Glycosamine
A sugar in which an anomeric hydrogen is replaced by nitrogen.
Ribose and 2-Deoxyribose
Sugars found in RNA and DNA, respectively.
Glycolipids and Glycoproteins
Molecules on cell surfaces important for cell recognition and blood types.
Streptomycin
An antibiotic that inhibits bacterial protein synthesis enzymes.