Answer:
D-Glucose and L-Glucose
Explanation:
Aldohexose are the sugars which have six number of carbons and ends up in having an aldehyde group at one end. When dilute nitric acid is treated with any of them, the molecule gets oxidized (gets oxygen) and therefore turns into carboxylic acid.
The name of A is D-Glucose, and B is L-Glucose. Please find the structural formula attached.
Answer: D-glucose reacts with dilute nitric acid to give an aldaric acid that was optically active, i.e. did not contain a plane of symmetry.
Explanation:Treatment of aldoses with dilute nitric acid converts them into aldaric acids. The aldehyde function at one end of the molecule and the primary alcohol at the other are both oxidized to carboxylic acids.
Fischer had previously developed a method to interchange the ends of a sugar (the
aldehyde is converted to a CH2OH and the CH2OH is converted to an aldehyde, Fischer reasoned that if ends of 2 were
interchanged, a new L-aldohexose would be obtained. On the other hand, if the
ends of 3 were interchanged, the product would be the same (structure 3). When
the ends of (+)-glucose were interchanged a new sugar was obtained, which Fischer
named L-gulose. When the ends of (+)-mannose were interchanged, the product
was (+)-mannose. Therefore the structure of (+) glucose is structure 2, and
strucutre 3 is (+)-mannose!!!
