what are the functional groups of carbohydrates what are the functional groups of carbohydrates

Each of its four hydrogen atoms forms a single covalent bond with the carbon atom by sharing a pair of electrons. Direct link to zita18's post well determining by its a, Posted 7 years ago. Unfortunately there isn't a universally accepted definition for what makes up a carbohydrate. Direct link to Sualeha's post in case of fructose which, Posted 3 months ago. Which Biomolecules simply refers as "Staff of life" in the given macromolecules? Your cells convert carbohydrates into the fuel molecule ATP through a process called cellular respiration.. Again, this difference gives fructose different chemical and structural properties from those of the aldoses, glucose, and galactose, even though fructose, glucose, and galactose all have the same chemical composition: C6H12O6. In the human diet, trans fats are linked to an increased risk of cardiovascular disease, so many food manufacturers have reduced or eliminated their use in recent years. An example of a hydrophobic group is the non-polar methane molecule. By number of carbons: glyceraldehyde (triose), ribose (pentose), and glucose (hexose). No, single bonds stereoisomers such as some enatiomers are not interchangeably because they are stuck in the three dimension world, Looking at my notes from the "Properties of Carbon" module, I would say that. 2. Name or draw the following compounds: Identify some common functional groups found in organic molecules. Two monosaccharides link together to form a disaccharide. Glucose 2. Is sucrose functional group? To log in and use all the features of Khan Academy, please enable JavaScript in your browser. How can you identify a carbohydrate? Carbohydrates are an example of the many types of organic compounds. Alkanes While alkanes are not technically a functional group as there's nothing unique to them and they don't really have much of any chemistry associated with them, they are a backbone of organic molecules. Direct link to Scott's post What is the difference be, Posted 7 years ago. Carbohydrates usually contain a carbonyl (=O) and hydroxyl (OH) functional group. 1. If not, why not? In nature, only the L-forms of amino acids are used to make proteins. Is all groups hydrophilic except for the methyl and amino groups? Thus, propane, propene, and propyne follow the same pattern with three carbon molecules, butane, butane, and butyne for four carbon molecules, and so on. How are the carbohydrates classified? The hydrocarbons ethane, ethene, and ethyne serve as examples of how different carbon-to-carbon bonds affect the geometry of the molecule. Direct link to ujalakhalid01's post we have looked at the lin, Posted 7 years ago. Monosaccharides are the simplest form of carbohydrates and may be subcategorized as aldoses or ketoses. Accessibility StatementFor more information contact us [email protected] check out our status page at https://status.libretexts.org. Figure 4. Plants are able to synthesize glucose. Functional groups can be classified as hydrophobic or hydrophilic based on their charge and polarity characteristics. Direct link to Lauren Faulkner's post No. If you're seeing this message, it means we're having trouble loading external resources on our website. Some D forms of amino acids are seen in the cell walls of bacteria, but never in their proteins. Cellulose is not very soluble in water in its crystalline state; this can be approximated by the stacked cellulose fiber depiction above. Monosaccharides can quickly and easily form H-bonds with water and are readily soluble. Hydrogen bonds between functional groups (within the same molecule or between different molecules) are important to the function of many macromolecules and help them to fold properly into and maintain the appropriate shape for functioning. Short Answer. During ring formation, the, Linear and ring forms of glucose. This is also true for many disaccharides and many short-chain polymers. The name "carbohydrate" means a "hydrate of carbon." The name derives from the general formula of carbohydrate is C x (H 2 O) y - x and y may or may not be . Solution. Direct link to zita18's post please how comes the phos, Posted 4 years ago. Figure 6. Direct link to Gen L's post Why are galactose and glu, Posted 6 years ago. To log in and use all the features of Khan Academy, please enable JavaScript in your browser. Fructose 3. Direct link to Matt B's post The short molecules are s, Posted 6 years ago. 3. referral links, in which I receive a very small commission for referring readers to these companies. Answer 1) Carbohydrates are one of the three macronutrients (along with proteins and fats) that are essential for the human body. In a solution of water, around 3% will be in the linear form, the rest are ringed. Other functional groups, such as the carbonyl group, have a partially negatively charged oxygen atom that may form hydrogen bonds with water molecules, again making the molecule more hydrophilic. Another type of hydrocarbon, aromatic hydrocarbons, consists of closed rings of carbon atoms. Answer link a group of atoms. If the latter is true, why is deoxyribose a carbohydrate with a formula C5H10O4? An example of a hydrophobic group is the non-polar methane molecule. CLEAR AND SIMPLE - Learn how biomolecules (organic molecules) are chemically formed. As the backbone of the large molecules of living things, hydrocarbons may exist as linear carbon chains, carbon rings, or combinations of both. Molecules with other elements in their carbon backbone are substituted hydrocarbons. The macromolecules are a subset of organic molecules (any carbon-containing liquid, solid, or gas) that are especially important for life. Direct link to N Peterson's post A monomer is the smallest, Posted 6 years ago. While we may be most familiar with the role carbohydrates play in nutrition, they also have a variety of other essential functions in humans, animals, plants, and bacteria. What is the difference between a monomer and a monosaccharide? Unlike amylose, cellulose is made of glucose monomers in their form, and this gives it very different properties. This page titled 1.4: Carbon and Functional Groups is shared under a CC BY license and was authored, remixed, and/or curated by OpenStax. They are the most abundant organic molecules in nature and are also referred to as "saccharides". Carbohydrates are classified into three subtypes: monosaccharides, disaccharides, and polysaccharides. Direct link to William H's post In a solution of water, a, Posted 7 years ago. The next thing to address is how these compounds interact with other compounds. This exoskeleton is made of the macromolecule, Posted 7 years ago. Majority of the monosaccharides found in the human body are of which type . Lipids---carboxylic acid with long hydrocarbon chains (usually above 16 C long). Direct link to Akshat Khandelwal's post What does R' stands for? However, some herbivores, such as cows, koalas, buffalos, and horses, have specialized microbes that help them process cellulose. Maltose, or malt/grain sugar, is a disaccharide formed by a dehydration reaction between two glucose molecules. In this article we'll discuss functional groups of carbohydrates. The structure for one of the most common saccharides, glucose, is shown here. Browse functional groups biology resources on Teachers Pay Teachers, a marketplace trusted by millions of teachers for original educational resources. Carbonyl Functional Group; Carbohydrates. Also pictured ring forms of ribose and fructose. Carbohydrates can contain hydroxyl (alcohol) groups, ethers, aldehydes and/or ketones. Are all molecules with a carbonyl group (C=O) and hydroxyl group (OH) carbohydrates? A ketose signifies that the sugar contains a ketone functional group. D)Carbon is electronegative. Most of the carbohydrate, though, is in the form of starch, long chains of linked glucose molecules that are a storage form of fuel. A bit more of the potato's carbohydrate is in the form of fiber, including cellulose polymers that give structure to the potatos cell walls. Higher alkali molecular weight alcohols, aldehydes and ketones Elements Analysis Perform the sodium fusion test or the Lassaigne's Test for the presence or the absence of nitrogen, sulfur and halogens in the given organic sample. Monosaccharides 2. Just think of cellulose, a polymer of glucose, if you have any doubts. Thats great for plants, but what about us? Carbohydrates are simple sugar derivatives like glucose, fructose, and galactose that are linked together (or polymerized). For example, carbohydrates can have phosphates or amino groups substituted at a variety of sites within the molecule. In a polymer, because there are so many H-bonds, this can provide a lot of strength to the molecule or molecular complex, especially if the polymers interact. Carboxyl 3. Wood-chewing termites also break down cellulose with the help of microorganisms that live in their guts. Image of a bee. Several classifications of carbohydrates have proven useful, and are outlined in the following table. In this section, we will discuss and review basic concepts of carbohydrate structure and nomenclature, as well as a variety of functions they play in cells. These groups play an important role in the formation of molecules like DNA, proteins, carbohydrates, and lipids. Carbohydrates generally have multiple alcohol functional groups, so we never focus on those. Carbohydrates are organic compounds. These additional atoms allow for functionality not typically seen in hydrocarbons. Methane, an excellent fuel, is the simplest hydrocarbon molecule, with a central carbon atom bonded to four different hydrogen atoms, as illustrated in Figure \(\PageIndex{1}\). A: First calculate the number of moles for ammonia and then use mol to mol ratio to calculate the mass. Legal. Direct link to mark foster's post Are the groups that don't, Posted 6 years ago. We will look at the presence of functional groups in the more basic elements to see who are the functional groups involved in carbohydrates. There are three classes of carbohydrates: monosaccharides, disaccharides, and polysaccharides. Direct link to Ivana - Science trainee's post Because it requires break, Posted 7 years ago. They are structural isomers, meaning they have the same chemical formula (C6H12O6) but a different arrangement of atoms. Here we can identify multiple hydroxyl (alcohol) functional groups and one aldehyde functional group. For instance, in solution, glucoses main configuration is a six-membered ring. These chains cluster together to form parallel bundles that are held together by hydrogen bonds between hydroxyl groups. Similarly, the D-form of glucose is the main product of photosynthesis and the L-form of the molecule is rarely seen in nature. Probably not. This numbering is shown for glucose and fructose, above. Carbohydrates That Will Help You Lose Weight. Functional groups include: hydroxyl, methyl, carbonyl, carboxyl, amino, phosphate, and sulfhydryl. Starch (from the Old English word stercan, meaning "to stiffen") is found mostly in seeds, roots, and stems, where it is stored as an available energy source for plants. These functional groups can provide additional properties to the molecule and will alter its overall function. In the 5th paragraph, there is discussion about carboxyl groups and carboxylate and, although these have been discussed in previous videos, I noticed that I did not remember which was which. 22407 views Often, these additional atoms appear in the context of functional groups. There are compounds where phosphorous forms three bonds (this is associated with an oxidation state of +3 or -3), but this element seems to prefer an oxidation state of +5. Get detailed information including the Defin . Longer polymers may not be readily soluble. Simple carbohydrates can be classified based on the number of carbon atoms in the molecule, as with triose (three carbons), pentose (five carbons), or hexose (six carbons). Direct link to Michael's post Confused about difference, Posted 7 years ago. The remaining six functional groups in the table all have varying degrees of hydrophilic character. Key Terms hydrophobic: lacking an affinity for water; unable to absorb, or be wetted by water . Monosaccharides are the simplest carbohydrates and cannot be hydrolyzed into other smaller carbohydrates. Glycogen is usually stored in liver and muscle cells. For example, due to their different chemical properties, butane is suited for use as a fuel for cigarette lighters and torches, whereas isobutene is suited for use as a refrigerant and a propellant in spray cans. Amino groups are polar so they are also hydrophilic. The former sugars are called aldoses based on the aldehyde group that is formed; the latter is designated as a ketose based on the ketone group. Glycogen is a common stored form of glucose in humans and other vertebrates. This gives cellulose its rigidity and high tensile strengthwhich is so important to plant cells. Simple carbohydrates are classified into three subtypes: monosaccharides, disaccharides, and polysaccharides, which will be discussed below. Molecules that share the same chemical formula but differ in the placement (structure) of their atoms and/or chemical bonds are known as isomers. (The reaction also releases a water molecule, not pictured.). For the formation of molecules like proteins, carbohydrates, lipids, and DNA, the functional groups that are hydroxyl, methyl carbonyls . To be enantiomers, a molecule must have at least three different atoms or groups connected to a central carbon. That may seem odd because sugars are often drawn as rings. This basic structure accounts for two of the four functional groups. Then it would be exactly like galactose. Identify the functional groups for the following organic molecules. 3. These provide the potato, and the person eating the potato, with a ready fuel source. Can you suggest a reason for why (based on the types of interactions) it might be so insoluble? If you're seeing this message, it means we're having trouble loading external resources on our website. Because of this small difference, they differ structurally and chemically and are known as chemical isomers because of the different arrangement of functional groups around the asymmetric carbon; both of these monosaccharides have more than one asymmetric carbon (compare the structures in the figure below). Lipids with Hydrophilic Groups 3. Answer (1 of 5): Glycerol, or glycerine, is a tri-alcohol or polyol in that it has three hydroxy (OH) functional groups (see diagram). Monosaccharides Monosaccharides are simple sugars. Functional groups include: hydroxyl, methyl, carbonyl, carboxyl, amino, phosphate, and sulfhydryl. Each carbon atom in a monosaccharide is given a number, starting with the terminal carbon closest to the carbonyl group (when the sugar is in its linear form). Lastly, we must consider functional groups that arise through the linking of saccharides. General names for carbohydrates include sugars, starches, saccharides, and polysaccharides. This results in a filled outermost shell. This carbon backbone is formed by chains and/or rings of carbon atoms with the occasional substitution of an element such as nitrogen or oxygen. Some of the important functional groups in biological molecules include: hydroxyl, methyl, carbonyl, carboxyl, amino, phosphate, and sulfhydryl groups. 0 0 Functional groups in biological molecules play an important role in the formation of molecules like DNA, proteins, carbohydrates, and lipids. In a sucrose molecule, the. 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. A covalent bond formed between a carbohydrate molecule and another molecule (in this case, between two monosaccharides) is known as a glycosidic bond. The answer to that is that it depends on the final structure of the carbohydrate. Figure \(\PageIndex{4}\): Which of the following statements is false? Are the groups that don't specify if they are charged or uncharged just neither? This carboxyl group ionizes to release hydrogen ions (H+) from the COOH group resulting in the negatively charged COO- group; this contributes to the hydrophilic nature of whatever molecule it is found on. Starch is the stored form of sugars in plants and is made up of a mixture of amylose and amylopectin; both are polymers of glucose. Wood and paper are mostly cellulosic in nature. Organic Chemistry Uttarakhand Open University. Glucose in a ring form can have two different arrangements of the hydroxyl group (OH) around the anomeric carbon (C1 that becomes asymmetric in the process of ring formation). The bee's exoskeleton (hard outer shell) contains chitin, which is made out of modified glucose units that have a nitrogenous functional group attached to them. Hydrogen bonds are also involved in various recognition processes, such as DNA complementary base pairing and the binding of an enzyme to its substrate, as illustrated in Figure \(\PageIndex{8}\). Stereochemistry of the compound. Individual carbon atoms have an incomplete outermost electron shell. What functional groups are found in carbohydrates? Fats with at least one double bond between carbon atoms are unsaturated fats. Direct link to V1dotra1's post How can you tell if a fun, Posted 4 years ago. The most common disaccharide is sucrose, or table sugar, which is composed of the monomers glucose and fructose. Q: Urea (HNCONH) is used extensively as a nitrogen source in fertilizers. Glycogen is the animal equivalent of starch and is a highly branched molecule usually stored in liver and muscle cells. 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. Figure 7. Furthermore, the overall geometry of the molecule is altered by the different geometries of single, double, and triple covalent bonds, illustrated in Figure \(\PageIndex{2}\). Functional groups can be classified as hydrophobic or hydrophilic based on their charge and polarity characteristics. The many covalent bonds between the atoms in hydrocarbons store a great amount of energy, which is released when these molecules are burned (oxidized). What are carbohydrates functional groups? Polysaccharides are often organized by the number of sugar molecules in the chain, such as in a monosaccharide, disaccharide, or trisaccharide. Classification according to Functional group Aldose sugars having an aldehyde functional group R-HC=O Ketose sugars having a ketone functional group R 2 -C=O In sucrose, a glycosidic linkage is formed between the C1 carbon in glucose and the C2 carbon in fructose. In cellulose, glucose monomers are linked in unbranched chains by 1-4 glycosidic linkages. Functional groups are groups of atoms that occur within molecules and confer specific chemical properties to those molecules. When the ring forms, the side chain it closes on is locked into an or position. The suffixes -ane, -ene, and -yne refer to the presence of single, double, or triple carbon-carbon bonds, respectively. The starch in the seeds provides food for the embryo as it germinates and can also act as a source of food for humans and animals who may eat the seed. Functional groups are found along the "carbon backbone" of macromolecules which is formed by chains and/or rings of carbon atoms with the occasional substitution of an element such as nitrogen or oxygen. Cellulases can break down cellulose into glucose monomers that can be used as an energy source by the animal. The first one, called a hydrocarbon functional group, consists of atoms of hydrogen and carbon. Cellulose is specific to plants, but polysaccharides also play an important structural role in non-plant species. Because carbohydrates have many hydroxyl groups associated with the molecule, they are therefore excellent H-bond donors and acceptors. Because it requires breaking off the bonds. As illustrated in Figure 6, amylose is starch formed by unbranched chains of glucose monomers (only 1-4 linkages), whereas amylopectin is a branched polysaccharide (1-6 linkages at the branch points). in case of fructose which is a pentose sugar how can we distinguish between alpha and beta fructose? As shown in the figure above, every other glucose monomer in the chain is flipped over in relation to its neighbors, and this results in long, straight, non-helical chains of cellulose. Some of the important functional groups in biological molecules are shown above: hydroxyl, methyl, carbonyl, carboxyl, amino, phosphate, and sulfhydryl (not shown). Carbohydrates That Will Help You Lose Weight What Do You Need To Know About Carbohydrates? Because of the way the subunits are joined, the glucose chains in amylose and amylopectin typically have a helical structure, as shown in the diagram below. Direct link to RogerP's post Amino groups are polar so, Posted 6 years ago. Monosaccharides. Most large biological molecules in fact contain many types of atoms beyond just carbon and hydrogen. Cellulose is the most abundant natural biopolymer. For instance, the diagram below shows glucose and fructose monomers combining via a dehydration reaction to form sucrose, a disaccharide we know as table sugar. Carbohydrates can contain hydroxyl (alcohol) groups, ethers, aldehydes and/or ketones. They are subdivided into two classes aldoses and ketoses on the basis of whether they are aldehydes or ketones. Although energy storage is one important role for polysaccharides, they are also crucial for another purpose: providing structure. Many people can't digest lactose as adults, resulting in lactose intolerance (which you or your friends may be all too familiar with). Acetals, hemiacetals, ketals and hemiketals in drug metabolism. All carbohydrates contain alcohol functional groups, and either an aldehyde or a ketone group (or a functional group that can be converted to an . Carbohydrates are called saccharides or, if they are relatively small, sugars. Ring structures are found in hydrocarbons, sometimes with the presence of double bonds, which can be seen by comparing the structure of cyclohexane to benzene in Figure \(\PageIndex{3}\). 1. In the trans configuration, the carbons form a more or less linear structure, whereas the carbons in the cis configuration make a bend (change in direction) of the carbon backbone. Group of atoms that give specific characteristics to an element. { "01.1:_Welcome_to_BIS2A" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "01.2:_The_Scientific_Method" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "01.3:_Problem_Solving" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "02.1:_The_Design_Challenge" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "02.2:_Bacterial_and_Archaeal_Diversity" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "02.3:_Eukaryotic_Cell:_Structure_and_Function" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "03.1:_Electronegativity" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "03.2:_Bond_TypesIonic_and_Covalent" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "03.3:_Hydrogen_Bonds" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "03.4:_Functional_Groups" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "04.1:_Carbohydrates" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "04.2:_Lipids" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "04.3:_Amino_Acids" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "04.4:_Nucleic_Acids" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "05.1:_Proteins" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "05.2:_Enzymes" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "05.3:_pH" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "06.1:_pKa" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "06.2:_Chemical_Reactions" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "06.3:_Energy_Story" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "06.4:_Thermodynamics" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "06.5:_Energy" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "06.6:_Free_Energy" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "06.7:_Endergonic_and_Exergonic_Reactions" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "06.8:_Activation_Energy" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "07.1:_Energy_Story" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "07.2:_Energy_and_Chemical_Reactions" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "07.3:_Chemical_EquilibriumPart_1:_Forward_and_Reverse_Reactions" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "07.4:_Chemical_EquilibriumPart_2:_Free_Energy" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "08.1:_ATP" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "08.2:_Reduction_Oxidation_Reactions" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "08.3:_Electron_Carriers" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "09.1:_Metabolism_in_BIS2A" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "09.2:_Glycolysis:_Beginning_Principles_of_Energy_and_Carbon_Flow" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "09.3:_Fermentation_and_Regeneration_of_NAD" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "10.1:_Oxidation_of_Pyruvate_and_the_TCA_Cycle" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "10.2:_Introduction_to_Electron_Transport_Chains_and_Respiration" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "11.1:_Electron_Transport_Chains" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "11.2:_Light_Energy_and_Pigments" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "11.3:_Photophosphorylation:_Anoxygenic_and_Oxygenic" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "12:_Light_Independent_Reactions_and_Carbon_Fixation" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "13.1:_Eukaryotic_Origins" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "14:_The_Cytoskeleton" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "15.1:_Membranes" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "15.2:_Membrane_Transport" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "15.3:_Membrane_Transport_with_Selective_Permeability" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "16.1:_The_DNA_Double_Helix_and_Its_Replication" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "17.1:_The_Flow_of_Genetic_Information" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "18.1:_Transcriptionfrom_DNA_to_RNA" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "19.1:_TranslationProtein_Synthesis" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "19.2:_The_Endomembrane_System" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "20.1:_Mutations_and_Mutants" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "21.1:_Sickle_Cell_Anemia" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "22.1:_Gene_regulation:_Introduction" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "23.1:_Gene_regulation:_Bacterial" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "23.2:_Gene_regulation:_Eukaryotic" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "24.1:_Cell_division:_Bacterial" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "24.2:_Cell_division:_Mitosis" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "25.1:_Cell_division:_Mitosis" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "25.2:_Cell_division:_Meiosis" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "26:_Genomes:_a_Brief_Introduction" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()" }, { Bis2A_SS2_Lecture_Agenda : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", Readings : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()" }, https://bio.libretexts.org/@app/auth/3/login?returnto=https%3A%2F%2Fbio.libretexts.org%2FCourses%2FUniversity_of_California_Davis%2FBIS_2A%253A_Introductory_Biology_(Easlon)%2FReadings%2F04.1%253A_Carbohydrates, \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}}}\) \( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash{#1}}} \)\(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\) \(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\)\(\newcommand{\AA}{\unicode[.8,0]{x212B}}\), Fructose versus both glucose and galactose, Linear versus ring form of the monosaccharides, status page at https://status.libretexts.org, Simple carbohydrates, such as glucose, lactose, or dextrose, end with an "-ose.".