Monosaccharides
⮚Monosaccharides are the simplest form of
Carbohydrates. These monosaccharides are the simple sugar having the molecular
formula Cn(H20)n and cannot be hydrolyzed further.
⮚These monosaccharides are linked by special type
of covalent bond called glycosidic bond. Two monosaccharide monomers are linked
to form the Disaccharide. Two to ten monosaccharide monomers are linked to form
the Oligosaccharide. Several monomers are linked to form the Polysaccharides.
⮚Based on the number of carbon atom the
monosaccharides are further divide into Trioses, Tetroses, Pentoses, Hexoses,
Heptoses.
⮚Based on the function group it divided into
aldoses (Ex: Glyceraldehyde, Glucose) and ketoses (Ex: dihydroxy acetone,
fructose).
⮚Examples for the monosaccharides are Glucose,
Fructose and Galactose.
⮚Glucose is one of the most common monosaccharide
that is abundant in nature. In 1747 Andreas Marg Graff was first isolated. It
is sweet in taste and crystalline in structure and are soluble in water.
⮚Glucose is composed of 6 carbon molecules. It
can be broken down in Glycolysis cycle. It provides energy and helps in
cellular respiration. If cell doesn’t need energy it will be stored in liver
and muscles.
⮚The molecular structure of Glucose is C6H12O6. It can exist in
both straight and chain structure. Glucose is a reducing sugar.
Fructose
⮚It was discovered by French chemist name
Augustin in 1847. Fructose has higher solubility then others.
⮚It is also known as fruit sugar is a simple
ketonic molecules found in many plants. Fructose contains ketone as the
functional group.
⮚Fructose can combine with Glucose by glycosidic
bond to form a Disaccharide called Sucrose.
Galactose
⮚It is commonly called as milk sugar. Galactose
exist in both cyclic and open chain form. Galactose is widely found in dairy products,
Avogadro’s, Sugars, Beets.
⮚Galactose is also synthesized by the body. Where
it forms of Glycolipids &Glycoproteins in several tissues. Galactose
combine with glucose to from a disaccharide called lactose.
Reactions of monosaccharides
Tautomerization:
➣It is the process of shifting a hydrogen atom
from One carbon atom to another to produce enediols is known as
Tautomerization.
➣Glucose Kept in alkaline solution for several
hours, it undergoes isomerization to form D-fructose and D-Mannose.
Oxidation:
➣Depending on the oxidizing agent used, the
terminal aldehyde or keto or alcohol groups may be oxidized.
➢Oxidation of aldehyde results in the form of
Gluconic acid.
CHO → COOH
Reduction:
When treated with reducing agents such as
amalgam, sodium the aldehyde or keto group of monosaccharides is reduced to
alcohol.
Dehydration:
When treated with concentrated H2SO4 monosaccharides
undergo dehydration with an elimination of 3H20 molecules.
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