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A tetrose is a monosaccharide with 4 carbon atoms.
They either have an aldehyde functional group in position 1 (aldotetroses) or a ketone functional group in position 2 (ketotetroses).
The aldotetroses have two chiralatrial centres ("asymmetric carbon atoms") and so 4 different stereoisomers are possible.
The naturally occurring aldotetroses are:
The 2 D-aldotetroses are:
CH=O CH=O | | HC-OH HO-CH | | HC-OH HC-OH | | CH2OH CH2OH D-Erythrose D-Threose
The ketotetroses have 1 chiral centres and therefore 2 possible stereoisomers — Erythrulose (L- and D-form).
The D-ketotetrose is:
CH2OH | C=O | HC-OH | CH2OH D-Erythrulose
The only naturally occurring ketotetrose is D-erythrulose.
See also
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- This page was last modified on 6 July 2008, at 13:00.
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