Carbs are classified as single sugars, disaccharides, or polysaccharides carbohydrates.
Monosaccharides are aldehydes or ketones of polyhydroxy.
In their count of carbonic atoms monosaccharides are also classified: triosis, tetrosis, pentose, or hexoses.
Chiral molecules are mirror-imaged molecules that do not overlap.
These stereoisomer types are referred to as enantiomers.
At least one chiral carbon must be a chiral molecule that is a carbon bonded to 4 different atoms or groups of atoms.
The Fischer project is a simplified way of arranging atoms, placed at a crossroads between vertical and horizontal lines by placing carbon atoms.
The − OH group is to the right of the chiral carbon away from the carbonyl group in a d enantiomer; the − OH group is to the left in the l enantiomer
Aldohexoses, glucose and galactose as well as ketohexose, fructose are important monosaccharides.
A ring of five or six atoms is the predominant form of a monosaccharide.
The cyclic structure forms if a − − OH group reacts with the same molecule carbonyl group (normally one on carbon-5 hexoses).
Cyclic monosaccharide isomers are produced by the formation of a new hydroxy group for carbon 1.
In an aldose, the aldehyde group is oxidized into a carboxylic acid, while in an aldose or ketosis the carbonyl group can be reduced to the hydroxyl group.
The monosaccharides which reduce sugars have an open-chain aldehyde group that is oxidizable.
Disaccharides are two units combined by a glycosidic bond.
There is at least one glucose unit in the common disaccharides maltose, lactose, and sucrose
Maltose and lactose form an isomer and b, which reduces sugar.
Sucrose has no isomers and is not sugar reduction
Polysaccharides are monosaccharide polymers
Glycogen is more branched, like amylopectin
Cellulose is also a glucose polymer, but b(1S4) bonds are the glycoside bond in cellulose.