Draw the structure of each of the following compounds:a. a polysaccharide formed by joining D-glucosamine in 1->6-a-glycosidic linkagesb. a disaccharide formed by joining D-mannose and D-glucose in a 1->4-ß-glycosidic linkage using mannose’s anomericcarbonc. an a-N-glycoside formed from D-arabinose and C6H5CH2NH2d. a ribonucleoside formed from D-ribose and thymine
Carbohydrates
Carbohydrates are the organic compounds that are obtained in foods and living matters in the shape of sugars, cellulose, and starch. The general formula of carbohydrates is Cn(H2O)2. The ratio of H and O present in carbohydrates is identical to water.
Starch
Starch is a polysaccharide carbohydrate that belongs to the category of polysaccharide carbohydrates.
Mutarotation
The rotation of a particular structure of the chiral compound because of the epimerization is called mutarotation. It is the repercussion of the ring chain tautomerism. In terms of glucose, this can be defined as the modification in the equilibrium of the α- and β- glucose anomers upon its dissolution in the solvent water. This process is usually seen in the chemistry of carbohydrates.
L Sugar
A chemical compound that is represented with a molecular formula C6H12O6 is called L-(-) sugar. At the carbon’s 5th position, the hydroxyl group is placed to the compound’s left and therefore the sugar is represented as L(-)-sugar. It is capable of rotating the polarized light’s plane in the direction anticlockwise. L isomers are one of the 2 isomers formed by the configurational stereochemistry of the carbohydrates.
Draw the structure of each of the following compounds:
a. a polysaccharide formed by joining D-glucosamine in 1->6-a-glycosidic linkages
b. a disaccharide formed by joining D-mannose and D-glucose in a 1->4-ß-glycosidic linkage using mannose’s anomeric
carbon
c. an a-N-glycoside formed from D-arabinose and C6H5CH2NH2
d. a ribonucleoside formed from D-ribose and thymine
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