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aldose sugars
the first carbon has an aldehyde

ketose sugars
the second carbon is a ketone

D Fisher Projection
the position of the hydroxyl group at the terminal position or the chiral center furthest from the first carbon is on the right
L Fisher Projection
the position of the hydroxyl group at the terminal position or the chiral center furthest from the first carbon is on the left
D-glucose

D-fructose

D-ribose

epimers
change occurs at one chiral center
D and L are enantimers
flip the stereochemistry at every carbon
substituents on the left go…
up or above the plane
substituents on the right go…
down or below the plane
anomeric carbon
the carbon that was the carbonyl, has the same oxidation state
only carbon in a cyclic structure that is bonded to two oxygen
alpha monosaccaride
CH2OH is on different side as the reactive OH
beta monosaccaride
CH2OH is on the same side as the reactive OH