It is found also that some monosaccharoses behave as aldehydes whilst others contain a keto group; those having the first character are called aldoses, and the others ketoses.
It is seen that aldoses and ketoses which differ stereochemically in only the two final carbon atoms must yield the same osazone; and since d-mannose, d-glucose, and d-fructose do form the same osazone (d-glucosazone) differences either structural or stereochemical must be placed in the two final carbon atoms.3 It may here be noticed that in the sugars there are asymmetric carbon atoms, and consequently optical isomers are to be expected.
The configurations of the pentaand tetra-aldoses have been determined by similar arguments; and those of the ketoses can be deduced from the aldoses.
Cane sugar has no reducing power and does not form an hydrazone or osazone; the other varieties, however, reduce Fehling's solution and form hydrazones and osazones, behaving as aldoses, i.e.
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