The disaccharide maltose is shown below. It contains an a-1,4'-glycosidic linkage between two sugars. Number the carbons on each using the correct numbering scheme for sugars (the sugar on the right should be numbered 1', 2', 3', etc.). Circle the glycosidic bond. Name the two monosaccharides that make up maltose. OH Sugar 1 (left): Sugar 2 (right): Type of glycosidic bond: HO HO Sugar: Type of glycosidic bond: HO- OH Sugar 1 (left): Sugar 2 (right): Name the two monosaccharides that comprise lactose (shown below). Number the carbons. Name the type of glycosidic bond. HOOH HO O HO HO OH OH HO- Name the monosaccharide and the type of glycosidic bond in the polysaccharide galactan shown below. 0 OH HOO OH HO- OH OH OH OH OH
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.
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