2. If the sugar can be broken down by hydrolysis, in the third column list the common names of the simple sugar Separate each name with a comma. If the sugar can't be broken down by hydrolysis, check the does not hydrc name and type of this sugar results of hydrolysis of this sugar description name: names: | This sugar is plentiful in milk, but not in fermented milk monosaccharide O does not hydrolyze products like cheese or yogurt, since it's consumed by the bacteria used to make those O disaccharide products. polysaccharide reducing sugar name: Sucrose names: monosaccharide does not hydrolyze This sugar is often called table disaccharide sugar. O polysaccharide reducing sugar names: name: Glucose O does not hydrolyze This sugar is often called dextrose, particularly in industrial chemistry and monosaccharide disaccharide medicine. polysaccharide O reducing sugar Explanation Check 2021 McGraw-Hill E
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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