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Reducing sugarsModerator: BioTeam
3 posts • Page 1 of 1
Reducing sugarsOkay, I understand that reducing sugars are such that they reduce Cu III to Cu+ ions, as in a Benedict’s solution. This reduction is due to the double bonded =O in the Aldehyde, and Keytone groups. What I do not get is how this reaction occurs when the monosaccharide like say glucose forms a ring which it does when in a hydrated medium. In a ring form the =O gets an H from the #5 Carbon to make =OH. In this configuration I do not see how a reaction can occur. So what gives ?
One more question. Since a starch is a chain of monosaccharides, howcome it does not reduce. I would think the end of the starch chain would behave like a single glucose and react with the Cu. Thanks
1.It's not exclusively in a ring formation, you'll still have linear chains. Microscopic reversibility and equilibrium
2.It does, but only once per molecule only one site available at the ends. Assuming a weight by weight comparison, there's less reactions taking place. Living one day at a time;
Enjoying one moment at a time; Accepting hardships as the pathway to peace; ~Niebuhr
3 posts • Page 1 of 1
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