Ch 4: Carbohydrate Structure and Function Flashcards
carbohydrates are organized by their
number of carbon atoms and functional groups
common names are freq used when referring to sugars such as
glucose, fructose, galactose
3 carbon sugars are
trioses
4 carbon sugars are
tetroses
sugars with aldehydes as their most oxidized group are
aldoses
sugars with ketones as their most oxidized group are
ketoses
nomenclature of ___ is based on ___ of glyceraldehyde
sugars
D/L
sugars with the highest-numbered chiral carbon with the -OH group on the right are
D sugars
D/L forms of the same sugar are
enantiomers
diastereomers
nonsuperimposable configurations of molecules with similar connectivity. they differ at at least one- but not all- chiral carbons
include epimers and anomers
epimers
subtype of diastereomers that differ at exactly one chiral carbon
anomers
subtype of epimers that differ at the anomeric carbon
anomeric carbon
the new chiral center formed in a ring closure; it was the carbon containing the carbonyl in the straight-chain form
a-anomers have the -OH
on the anomeric carbon trans to the free -CH2OH aka its down in the water like a fish
b-anomers have the -OH on the anomeric carbon
cis to the free -CH2OH
Haworth Projections
provide a good way to represent 3D structures
mutarotation
switch from one anomer to the next with the straight chain form as an intermediate
Monosaccarides are single carbohydrate units, glucose being the most common monomer, can undergo 3 main reactions being
oxidation-reduction, esterification, and glycoside formation
aldoses can be oxidized to ___ and reduced to ___
aldonic acids
alditols
sugars that can be oxidized are ___ and can be detected with ____ or ____
reducing agents/reducing sugars
Tollen’s or
Benedict’s reagents
sugars can react with carboxylic acids and their derivatives forming ___. ___ is a similiar reaction in which phosphate ester is formed by transferring a phosphate group from ATP onto a sugar
esters (esterification)
phosphorylation
basis for building complex carbohydrates and requires the anomeric carbon to link to another sugar
glycoside formation
form as a result of glycosidic bonding btw 2 monosaccharide subuits
disaccharides
sucrose, common disaccharide, is
glucose-alpha-1,2-fructose
lactose, common disaccharides, is
galactose-B-1,4-glucose
maltose, common disaccharides, is
glucose-alpha-1,4-glucose
cellulose
polysaccharide that is main structural component for plant cell walls and is the main source of fiber in the human diet
starches (amylose and amylopectin)
polysaccharides that function as a main energy storage form for plants
glycogen
polysaccharide that functions as main energy storage form for animals