Introduction to Carbohydrates
Start with the big picture
Carbohydrates are classified by the number of saccharide units and, for monosaccharides, by carbon number and whether they contain an aldehyde or ketone group. Their stereochemistry includes D/L forms, epimers, and α/β anomers; interconversion of anomers in solution produces mutarotation. Reducing sugars have a free hemiacetal and can be detected with several reagents, while sucrose and trehalose are non-reducing because their anomeric groups are involved in glycosidic linkages. Tests such as Molisch, Seliwanoff, and Bial’s help screen or distinguish carbohydrate types. Natural polysaccharides also have practical roles: starch is a storage material, cellulose is used in tablet formulations, and inulin is a marker for glomerular filtration rate.
What you'll learn
- Classify carbohydrates by saccharide-unit count and monosaccharide structure.
- Distinguish D/L forms, epimers, anomers, and mutarotation.
- Explain reducing behavior and identify relevant carbohydrate tests.
- Describe key conversions and the properties of major natural polysaccharides.
Continue your study
Work through the complete notes and reinforce the topic with the study tools available in the full lesson.