A tetrose is a monosaccharide with 4 carbon atoms. They have either an aldehyde functional group in position 1 (aldotetroses) or a ketone functional group in position 2 (ketotetroses).
D-Erythrose
D-Erythrose
D-Threose
D-Threose
D-Erythrulose
D-Erythrulose
The aldotetroses have two chiral centers ("asymmetric carbon atoms") and so 4 different stereoisomers are possible. There are two naturally occurring stereoisomers, the enantiomers of erythrose and threose having the D configuration but not the L enantiomers. The ketotetroses have one chiral center and, therefore, two possible stereoisomers: erythrulose (L- and D-form). Again, only the D enantiomer is naturally occurring.
remember when we sold the horses their houses?
we stole a million more.
come back to where the thermostat is your best friend.
twelve hundred miles between here and there.