Describe the relationship between each of the pairs of isomers shown by recording Constitutional, Conformational, Enantiomers, Diastereomers, Identical or Meso. нн H;C CH3 H;CLCH, Constitutional CI H,CH H3C H. OH Enantiomers CH3 ČH3 Diastereomers Identical CH3 H3CH CIH H H. CH3 Meso `CH3 OH Conformational ÓH Not Related CH3 CH3 H H CI H H Br Br H3CH H CH3 H -CH3 H3C- Br Br CH3 CI H CH3 Br Br- -CH3 ČH3 CH3 он H- OH H- -CH3 -CH3 H- CH3 H- CH3 Br Br ČH3 H OH HOA H CH3 |||||
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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