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.
Ignoring chirality, draw the Haworth structure of allose. The open-chain Fischer projection for the monosaccharide is given here. Include only the hydrogen atoms attached to the oxygen atoms in the OH groups when drawing the cyclic form.
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Done A session.masteringchemis AA
<Homework Chapter 13
Drawing Cyclic Sugars
3 of 7
Part A
Ignoring chirality, draw the Haworth structure of
allose. The open-chain Fischer projection for the
monosaccharide is given here. Include only the
hydrogen atoms attached to
the oxygen atoms in the OH
groups when drawing the
cyclic form.
С-н
Н-С-ОН
Draw the molecule on the
Н-С-ОН
canvas by choosing
buttons from the Tools (for
bonds), Atoms, and
Advanced Template
toolbars. The single bond
is active by default.
Н-С-ОН
Н-С-ОН
ČH,OH
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