Science, Tech, Math › Science The Chemistry of Carbohydrates The Types, Functions, and Classifications of Carbohydrates Share Flipboard Email Print Adam Gault/Getty Images Science Chemistry Biochemistry Basics Chemical Laws Molecules Periodic Table Projects & Experiments Scientific Method Physical Chemistry Medical Chemistry Chemistry In Everyday Life Famous Chemists Activities for Kids Abbreviations & Acronyms Biology Physics Geology Astronomy Weather & Climate By Anne Marie Helmenstine, Ph.D. Anne Marie Helmenstine, Ph.D. Facebook Twitter Chemistry Expert Ph.D., Biomedical Sciences, University of Tennessee at Knoxville B.A., Physics and Mathematics, Hastings College Dr. Helmenstine holds a Ph.D. in biomedical sciences and is a science writer, educator, and consultant. She has taught science courses at the high school, college, and graduate levels. Learn about our Editorial Process Updated on March 08, 2019 Carbohydrates, or saccharides, are the most abundant class of biomolecules. Carbohydrates are used to store energy, though they serve other important functions as well. This is an overview of carbohydrate chemistry, including a look at the types of carbohydrates, their functions, and carbohydrate classification. List of Carbohydrates Elements All carbohydrates contain the same three elements, whether the carbohydrates are simple sugars, starches, or other polymers. These elements are: Carbon (C) Hydrogen (H) Oxygen (O) Different carbohydrates are formed by the way these elements bond to each other and the number of each type of atom. Usually, the ratio of hydrogen atoms to oxygen atoms is 2:1, which is the same as the ratio in water. What a Carbohydrate Is The word "carbohydrate" comes from the Greek word sakharon, which means "sugar". In chemistry, carbohydrates are a common class of simple organic compounds. A carbohydrate is an aldehyde or a ketone that has additional hydroxyl groups. The simplest carbohydrates are called monosaccharides, which have the basic structure (C·H2O)n, where n is three or greater. Two monosaccharides link together to form a disaccharide. Monosaccharides and disaccharides are called sugars and typically have names ending with the suffix -ose. More than two monosaccharides link together to form oligosaccharides and polysaccharides. In everyday usage, the word "carbohydrate" refers to any food that contains a high level of sugars or starch. In this context, carbohydrates include table sugar, jelly, bread, cereal, and pasta, even though these foods may contain other organic compounds. For example, cereal and pasta also contain some level of protein. The Functions of Carbohydrates Carbohydrates serve several biochemical functions: Monosaccharides serve as fuel for cellular metabolism.Monosaccharides are used in several biosynthesis reactions.Monosaccharides may be converted into space-saving polysaccharides, such as glycogen and starch. These molecules provide stored energy for plant and animal cells.Carbohydrates are used to form structural elements, such as chitin in animals and cellulose in plants.Carbohydrates and modified carbohydrates are important for an organism's fertilization, development, blood clotting, and immune system function. Examples of Carbohydrates Monosaccharides: glucose, fructose, galactose Disaccharides: sucrose, lactose Polysaccharides: chitin, cellulose Carbohydrate Classification Three characteristics are used to classify monosaccharides: Number of carbon atoms in the molecule Location of the carbonyl group The chirality of the carbohydrate Aldose - monosaccharide in which the carbonyl group is an aldehyde Ketone - monosaccharide in which the carbonyl group is a ketone Triose - monosaccharide with 3 carbon atoms Tetrose - monosaccharide with 4 carbon atoms Pentose - monosaccharide with 5 carbon atoms Hexose - monosaccharide with 6 carbon atoms Aldohexose - 6-carbon aldehyde (e.g., glucose) Aldopentose - 5-carbon aldehyde (e.g., ribose) Ketohexose - 6-carbon hexose (e.g., fructose) A monosaccharide is D or L, depending on the orientation of the asymmetric carbon located furthest from the carbonyl group. In a D sugar, the hydroxyl group is on the right the molecule when written as a Fischer projection. If the hydroxyl group is on the left of the molecule, it is an L sugar. Cite this Article Format mla apa chicago Your Citation Helmenstine, Anne Marie, Ph.D. "The Chemistry of Carbohydrates." ThoughtCo, Feb. 16, 2021, thoughtco.com/chemistry-of-carbohydrates-603878. Helmenstine, Anne Marie, Ph.D. (2021, February 16). The Chemistry of Carbohydrates. Retrieved from https://www.thoughtco.com/chemistry-of-carbohydrates-603878 Helmenstine, Anne Marie, Ph.D. "The Chemistry of Carbohydrates." ThoughtCo. https://www.thoughtco.com/chemistry-of-carbohydrates-603878 (accessed June 9, 2023). copy citation