sugars Flashcards
biologically active form of carbohydrates
D (dextrorotatory) - OH on right
aldotriose
glyceraldehyde
aldotetrose
erythrose
aldopentoses
xylose
arabinose
ribose
aldohexoses
galactose
mannose
glucose
ketotriose
dihydroxyacetone
ketopentoses
xyulose
ribulose
ketohexose
fructose
ketoheptulose
sedoheptulose
enanitomers
nonsuperimposable mirror image that have at least one chiral center
racemic mixture
equal amounts of 2 enanitomers; optically inactive
diastereomers
stereoisomers that are not mirror images
epimers
diastereomers that different around one chiral center
alpha configuration of haworth projection
OH down
beta configuration of haworth projection
OH up
mutarotation
inter conversion between alpha and beta forms
dehydration synthesis
builds carbohydrates by the covalent interaction of glycosidic bonds between monosaccharides
sugar phosphate esters
addition of a phosphate group (PO3 2-) to a monosaccharide
aldonic acid
oxidation of aldehyde group of aldose sugars to produce carboxyl group
uronic acid
oxidation of 1 (primary) hydroxyl group of monosaccharide to carboxyl group
lactones
internal esterification of monosaccharide derivatives to form 5 and 6 member rings
alditols
reduction of aldose or ketose carbonyl to hydroxyl group
deoxy-sugars
one monosaccharide hydroxyl group is replaces with H atom
amino sugars
hydroxyl group of monosaccharide is replaces with amine group