Chapter 13 - Carbohydrate
13.1 - Carbohydrates
- 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.
13.2 - Chiral Molecules
- 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.

13.3 - Fischer Projections of Monosaccharides
- 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.
13.4 - Haworth Structures of 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.
13.5 - Chemical Properties of Monosaccharides
- 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.
13.6 - Disaccharides
- 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

13.7 - Polysaccharides
- 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.
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