I Review| Co A10-L buffer solution is 0.125 Min HNO, and 0.170 Min NsNO2. Part A Determine the concentrations of HNO2 and NsNO2 after addition of 1.1 g HCl. Express your answers using three significant figures separated by a comma. undo redo re keyboard shortcuts help |HNO4). ĮNoNO2) = 0.158,0.137 Submit Pre vlou Anrı Requast AnENr X Incorrect: Try Again; 7 attempts remaining Part B Determine the concentrations of HNO, and NsNO, after addition of 1.1 g NaOH. Express your answers using three significart figures separated by a comma. famolares Symbols undo redo rest keyboard shortcuts help ver M HNO2). NaNO2) = Submit Request an r • Part C Determine the concentrations of HNO2 and NaNO2 after addition of 1.1 g HI. Express your answers using three significant figures separated by a comma. emplte ymbols undo redo rest keyboard shortouts help HNO2). NaNO2) = Submit Request an er P Pearson
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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