Chapter 10: Carbohydrates Flashcards
Carbohydrates
Carbon based molecules that are rich in hydroxyl (C - OH)
What is linkage of carbohydrates?
Glycosidic
Polysaccharides
Polymers of covalently linked monosaccharides
Monosaccharrides
Simplest carbohydrates
Cn(H20)n
Lowest n=3
Function of carbohydrates
- major energy sources: carbohydrate oxidation
- essential structural/ protective componets
- cell to cell recognition signals
Examples of monosaccharides
Dihydroxyacetone
D and L glyceraldehyde
Have 3 carbons
D Configuration
OH on right of highest numbered steric carbon
Mostly highly oxidized carbon is
C-1
L Configuration
OH on left of highest numbered steric carbon
In Haworth projection, D sugar CH2OH on C5
will be up
In Haworth projection, L sugar CH2OH on C5
will be down
Enantiomer
Nonsuperimposable mirror images
How to calculate streoisomer
of steroisomers = 2^n
n= # of chiral centers
Diasteroisomers
Isomers that are not mirror images
Epimers
Differ at only ONE carbon atom
Anomers
Isomers that differ at new asymmetric carbon after cyclization
Formation of a cyclic hemiacetal creates another
diastereoisomeric form
Anomeric carbon
Only carbon bonded to 2 oxygen atoms
Alpha form of anomers
Hydroxyl of C1 (anomeric carbon) is below the plane of ring
C5 of CH2OH and C1 of OH are opposite
Beta form of anomers
Hydroxyl of C1 (anomeric carbon) is above the plane of ring
C5 of CH2OH of C1 of Oh are on same side
Cyclization
OH attack C=O to form ring
Sugar alcohols (alditols)
carbonyl group of sugar is reduced to an alcohol (OH) group
Deoxy sugars
Reduced sugars where hydrogen atom is substitued for one of hydroxyl groups
Reducing sugars
Sugars that react with oxidizing agent
Tollens reagant test
Used to detect presence of reducing agent
Ag(NH3)2+ used as oxidizing agent