Carbohydrates are organic compounds represented by the formula (CH2O)n and are classified into monosaccharides, disaccharides, and polysaccharides. Monosaccharides like glucose are simple sugars, while disaccharides such as sucrose are formed from two monosaccharides through dehydration reactions. Polysaccharides, including starch and glycogen, are long chains of monosaccharides linked by glycosidic bonds, serving as energy storage in plants and animals.
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Carbohydrates are organic compounds represented by the formula (CH2O)n and are classified into monosaccharides, disaccharides, and polysaccharides. Monosaccharides like glucose are simple sugars, while disaccharides such as sucrose are formed from two monosaccharides through dehydration reactions. Polysaccharides, including starch and glycogen, are long chains of monosaccharides linked by glycosidic bonds, serving as energy storage in plants and animals.
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Carbohydrates
Carbohydrates can be represented by the formula (CH2O)n, where n is the
number of carbons in the molecule. In other words, the ratio of carbon to hydrogen to oxygen is 1:2:1 in carbohydrate molecules. This formula also explains the origin of the term “carbohydrate”: the components are carbon (“carbo”) and the components of water (hence, “hydrate”). Carbohydrates are classified into three subtypes: monosaccharides, disaccharides, and .polysaccharides Monosaccharides (mono– = “one”; sacchar– = “sweet”) are simple sugars, the most common of which is glucose. In monosaccharides, the number of carbons usually ranges from three to seven. Most monosaccharide names end with the –ose. If the sugar has an aldehyde group (the functional group with the structure R-CHO), it is known as an aldose, and if it has a ketone group (the functional group with the structure RC=O, it is known as a ketose. Depending on the number of carbons in the sugar, they also may be known as trioses (three carbons), pentoses (five carbons), and or hexoses .(six carbons) An Aldose contains an aldehyde with two or more hydroxyl groups attached; one of the hydroxyl groups is at end opposite to the aldehyde. An Aldose is a type of monosaccharide, which is plays a key role in the development of nucleic acids. The two simplest forms of Aldoses are L- and D-Glyceraldehydes, which are three-carbon structures that each contain one aldehyde and two hydroxyl groups. Aldoses can have three or more carbons. Aldoses are distinguishable by the carbonyl(C=O) group located at the end of the carbon chain, which differs from ketose, which has the .carbonyl group in the middle of the carbon chain This figure: Monosaccharides are classified based on the position of their carbonyl group and the number of carbons in the backbone. Aldoses have a carbonyl group (indicated in green) at the end of the carbon chain, and ketoses have a carbonyl group in the middle of the carbon chain. Trioses, pentoses, and hexoses .have three, five, and six carbon backbones The chemical formula for glucose is C6H12O6. In humans, glucose is an important source of energy. During cellular respiration, energy is released from glucose, and that energy is used to help make adenosine triphosphate (ATP). Plants synthesize glucose using carbon dioxide and water, and glucose in turn is used for energy requirements for the plant. Excess glucose is often stored as starch by humans and other animals that feed on .plants Galactose (part of lactose, or milk sugar) and fructose (part of sucrose, or fruit sugar) are other common monosaccharides. Although glucose, galactose, and fructose all have the same chemical formula (C6H12O6), they differ structurally and chemically because of the different arrangement of functional groups .around the carbon atom Disaccharides (di– = “two”) form when two monosaccharides undergo a dehydration reaction. During this process, the hydroxyl group of one monosaccharide combines with the hydrogen of another monosaccharide, releasing a molecule of water and forming a covalent bond. A covalent bond formed between a carbohydrate molecule and another molecule is known as .a glycosidic bond This figure. Sucrose is formed when a monomer of glucose and a monomer of fructose are joined in a dehydration reaction to form a glycosidic bond. In the process, a water molecule is lost. In sucrose, a glycosidic linkage is formed .between carbon 1 in glucose and carbon 2 in fructose Common disaccharides include lactose, maltose, and sucrose. Lactose is a disaccharide consisting of the monomers glucose and galactose. It is found naturally in milk. Maltose or malt sugar, is a disaccharide formed by a dehydration reaction between two glucose molecules. The most common disaccharide is sucrose or table sugar, which is composed of the monomers glucose and .fructose Polysaccharides
A long chain of monosaccharides linked by glycosidic bonds is
known as a polysaccharide (poly– = “many”). The chain may be branched or unbranched, and it may contain different types of monosaccharides. Starch, glycogen, cellulose, and chitin are .primary examples of polysaccharides Starch is the stored form of sugars in plants and is made up of a mixture of amylose and amylopectin. Plants are able to synthesize glucose, and the excess glucose, beyond the plant’s immediate energy needs, is stored as starch in different plant parts. The starch provides food for humans and animals. The starch that is consumed by humans is broken down by enzymes, such as salivary amylases, into smaller molecules, such as maltose and glucose. The cells can .then absorb the glucose Glycogen is the storage form of glucose in humans and is made up of monomers of glucose. Whenever blood glucose levels decrease, glycogen is broken down to release glucose in a process .known as glycogenolysis
Cellulose is the cell wall of plants is mostly made of cellulose;
this provides structural support to the cell. Cellulose is made up of .glucose monomers that are linked by glycosidic bonds Thank you