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Carbohydrates
Organic compounds consisting of carbon, hydrogen, and oxygen, typically with a hydrogen-oxygen atom ratio of 2:1.
Reducing sugars
Sugars that can donate electrons or reduce another compound, including all monosaccharides and some disaccharides.
Non-reducing sugars
Sugars that cannot act as reducing agents, as they do not have a free aldehyde or ketone group, such as sucrose.
Epimers
Diastereomers that differ in configuration at only one stereogenic center.
Mutarotation
The change in optical rotation that occurs when an α- or β-anomer of a sugar interconverts to the other form in solution.
Anomers
A type of stereoisomer that differs in configuration at the anomeric carbon.
Cyclic structure of glucose
Glucose exists primarily in a cyclic form, with a six-membered ring structure known as pyranose.
Haworth projection
A two-dimensional representation of the cyclic form of a sugar, showing the relative positions of atoms.
Inter conversions of sugars
The transformation between different sugar forms, such as converting aldoses to ketoses.
Kiliani-Fischer method
A synthetic method to elongate aldoses by adding a carbon chain at the reducing end.
Ruff's method
A method used to convert aldoses to ketoses and vice versa through oxidation and reduction.
Disaccharides
Carbohydrates composed of two monosaccharide units linked together by a glycosidic bond.
Sucrose
A common non-reducing disaccharide composed of glucose and fructose.
Maltose
A reducing disaccharide made up of two glucose units.
Lactose
A disaccharide sugar composed of one glucose and one galactose unit.