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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Balance Chemical E.
II Review | Constants | Periodic Table
A carbon atom is chiral if it is bonded to four different
groups. For example, CHCIBII is chiral, but CCl,BrI
is achiral because some of the bonded groups are the
same. If a chiral carbon atom is present, then that
molecule has a non-superimposable mirror image called
an enantiomer. (Figure 1)
Part A
Identify all the chiral atoms in the below structure by right-clicking* a chiral atom to bring
up a menu that includes "Atom Properties." Click on Atom Properties then click the
checked box next to the Map field to clear the checkmark. Then enter "1" in the Map
*Mac users: Use an equivalent for right-
field box to label that chiral carbon atom.
clicking.
>
• View Available Hint(s)
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