Epimers are carbohydrates that differ in the location of the -OH group in one location. Both D-glucose and D-galactose are the best examples. D-glucose and D-galactose epimers create a …

Anomers are cyclic monosaccharides or glycosides, differing from each other in the configuration of C−1 if they are aldose or in the configuration at C−2 if they are ketose.

Mutarotation is a difference in the specific rotation of plane-polarized light due to the change in the equilibrium between two anomers in the solution. Any molecule to show mutarotation must …

Structure Of Glucose and Fructose - Structure of Glucose can be represented either as an open chain or if folded into a ring known as pyranose ring. Fructose is a ketohexose sugar. The …

Q. α anomer of an aldohexose E has a specific rotation of 120∘ while β anomer of E has a specific rotation of 80∘. If an equilibrium mixture of α,β anomers of E has the specific rotation of 96∘, …

Isomerism in organic chemistry is a phenomenon shown by two or more organic compounds having the same molecular formula but different properties due to difference in arrangement of …

Conclusion Among structural isomers and stereoisomers, stereoisomers are optical active due to their presence of chiral centres. The main difference between diastereomers and enantiomers …

Amino acids are building blocks of proteins that play many important roles in the body. Technically, amino acids are organic compounds that contain the amine and carboxyl …

The correct option is D isomers of glucose that differ in configuration at carbon one (C - 1) Anomers are diastereoisomers of cyclic forms of sugars or similar molecules differing in the …

Enantiomers - Enantiomers are a pair of molecules that exist in two forms that are mirror images of one another but cannot be superimposed one upon the other. Enantiomers are in every …