Gulocose
Carbohydrates:-
Carbohydrates are the group of nutrients important in the diet as a source of energy they contain the elements carbon, hydrogen and oxygen and are produced in plants by the process of photosynthesis which may be represented by the following equation
(Chlorophyll)

Carbon dioxide water from (Sunlight/solar energy) glucose oxygen released from the air the soil in the air other carbohydrate
Classification of carbohydrates:-
There are various different carbohydrate but they may be divided into three group according to the size of molecule
1. Monosaccharide:-
The monosaccharide sugars are commonly found in food contain six carbon atom and have the general formula C6H12O6 .the three most important group are
C6H12O6+H 2O no reaction
(a) Glucose (Dextrose):-
The structure of a glucose molecule is shown in fig in the convention representation of the carbon atom in the ring are omitted. Glucose is found in varying amounts in fruits and vegetable. the large amount are found in fruits such as grapes and smaller quantities in vegetable such as young peas and carrots .it is also found in the blood of animal. Glucose syrup or commercial glucose is not pure glucose but a mixture of glucose, other carbohydrates and water Glucose is monosaccharide is an important carbohydrate in biology. The cell uses it as a source of energy and metabolic intermediate. Glucose is one of the main products of photosynthesis and starts cellulose respiration. The name comes from Greek language which means sweet carbohydrate. Glucose is commonly available in the form of a white substance or as a solid crystal. It can be commonly found as an aqueous solution.
Structure:-
Glucose (C6H12O6) contains six carbon atoms and an aldehyde group and is therefore referred as an aldohexose.the glucose molecule can exist in an open chain (acyclic0and ring (cyclic) form (in equibilirium), the latter be the result of intermolecular reaction between the aldehyde carbon atom and the C-5 hydroxyl group to form an inter molecular hemi acetyl in water solution both forma are in equilibrium
Function:-
We can speculate on the reasons why glucose, and not another monosaccharide such as fructose (Fru), is so widely used in evolution, the ecosystem, and metabolism. Glucose can form from formaldehyde under abiotic conditions, so it may well have been available to primitive biochemical systems. Probably more important to advanced life is the low tendency of glucose, by comparison to other hexose sugars, to non-specifically react with the amino groups of proteins. This reaction (glycation) reduces or destroys the function of many enzymes. The low rate of glycation is due to glucose's preference for the less reactive cyclic isomer. Nevertheless, many of the long-term complications of diabetes (e.g., blindness, kidney failure, and peripheral neuropathy) are probably due to the glycation of proteins or lipids. In contrast, enzyme-regulated addition of glucose to proteins by glycosylation is often essential to their function.
2. Disaccharides:-
The sugars have the general formula C12H22O11 .They are formed when two monosaccharide molecule combine with the elimation of water molecule
C6H12O6+C6H12O6 C12H22O11+H2O
This is an e.g. of a condensation reaction i.e. a reaction in which two small molecule combine to form one larger molecule with the elimination of a small molecule usually water from between them
Formation of disaccharides
Glucose +fructose = sucrose +water
Glucose+ galactose = lactose +water
Glucose +glucose = maltose+ water
Disaccharides are the simplest polysaccharides .they are composed of two monosaccharide units are bound together by a covalent bond formed via a dehydration reaction ,resulting in the loss of hydrogen atom from one mono
Saccharides and a hydroxyl group from the other, so the formula of general disaccharides is C12H22O11 .
3. Polysaccharides:-
Polysaccharides are a condensation polymers of monosaccharide and are made up of a many monosaccharide molecule joined together with the elimination of water molecule at each link they have the general formula (C6H10O5)n where n represent a large molecule.
Starch is the major food reserved of plants it is in fact the mixture of two polysaccharides
Types Of Glucose:-
D-Glucose:-
One form of glucose is simply called D-glucose. The "D" refers to the arrangement of alcohol, or OH, groups on the carbon skeleton of the sugar. D-glucose is an open-chain molecule consisting of six carbons arranged into a molecular backbone. There are five OH groups attached to this carbon backbone, forming "arms" or branches off the carbon skeleton. This form of glucose also has an aldehyde group at the top of the carbon skeleton, which consists of an atom of carbon with a double bond to an atom of oxygen, and a single bond to an atom of hydrogen.
Beta-D-Glucopyranose:-
A second form of glucose is called beta-D-glucopyranose. As in straight chain D-glucose, the "D" refers to the arrangement of alcohol groups on the carbon skeleton. Unlike D-glucose, beta-D-glucopyranose has a cyclic carbon skeleton. The ring structure that forms the backbone of the molecule consists of five carbon atoms and one oxygen atom.
Alpha-D-Glucopyranose:-
The final form of glucose in the body and in nature is alpha-D-glucopyranose. Drs. Mary Campbell and Shawn Farrell, authors of the 2005 text "Biochemistry," explain that the difference between alpha- and beta-D-glucopyranose lies in the orientation of a single alcohol group around the cyclic carbon backbone. This difference, while it seems minor, is actually very significant. Alpha-D-glucopyranose can be found in solution, or combined with other molecules of sugar. Digestible starch is made of many hundreds of linked alpha-D-glucopyranose units, for instance. Humans can split an alpha-linkage, but not an a beta-linkage, which explains why starch is digestible, but dietary fiber is not.