reducing and non reducing sugars slidesharepremier towing and recovery raeford nc

Non-reducing sugar is determined by subtracting the total reducing sugar from reducing sugar and multiplying the remainder with 0.95 factor. They are also found in fungi which rot wood. In particular, we'll recall how hemiacetals are converted to acetals. organic chemistry - How do you identify reducing / non-reducing sugar Tap here to review the details. Is Sucrose a reducing sugar? The aldehyde and ketone present on the monomers are involved in the formation of the glycosidic bond in the case of most disaccharides and all polysaccharides. It has distinct advantages over other sugars as storage and transport form. We nemen geen verantwoordelijkheid voor de inhoud van een website waarnaar we linken, gebruik je eigen goeddunken tijdens het surfen op de links. Starch is a polysaccharide composed of multiple monomeric units of glucose linked together by -1,4 linkages. Sixth Edition. These sugars have the capability to reduce the cupric ions into cuprous ions of the benedict's solution. The best answers are voted up and rise to the top, Not the answer you're looking for? Folate. Reducing sugars are the sugars which has free anomeric carbon which can reduce certain reagents and gets oxidised. The presence of reducing sugars is determined chemically by test methods such as dinitrosallicillic (quantitative) and qualitative methods using Benedicts reagent, Fehlings solution and Tollens reagent. The main non-reducing sugar is sucrose, or more commonly known as table sugar. A hemiacetal form is thus a reducing sugar. A disaccharide is formed from two monosaccharides (here, two molecules of D-glucose) when - Title: PowerPoint Presentation Author: George Koch Last modified by: Rutherford County Schools Created Date: 3/28/2004 11:42:54 PM Document presentation format. A password reset link will be sent to you by email. Glucose, fructose, and galactose are monosaccharides and are all reducing sugars. For instance, sucrose is a disaccharide but it is a non-reducing sugar. An important and simple test for identifying blood glucose is where an aldehyde reduces a Cu2+ ion (as in Benedict's solution) and a colour change occurs. The benedicts and feeling solution test is used to confirm the reducing sugars. Identifying reducing / non-reducing sugar been confusing me for a while now , I know that reducing sugar contain aldehyde or ketone group . 1. - Sugar alcohols (alditols): sweet-tasting, from mild reduction of sugars the chemical and physical properties of proteins, altering solubility, mass, - Starch is storage unit for solar energy. 3. stereo - 6th Edition Paula Yurkanis Bruice Chapter 22 The Organic Chemistry of Carbohydrates *, CHE 242 Unit VII The Physical and Chemical Properties, and Reactions of Ketones, Aldehydes, and Amines CHAPTER TWENTY-THREE, - CHE 242 Unit VII The Physical and Chemical Properties, and Reactions of Ketones, Aldehydes, and Amines CHAPTER TWENTY-THREE Terrence P. Sherlock Burlington County College. 22. Enter the username or e-mail you used in your profile. Fehling's test is a chemical test used to differentiate between reducing and non-reducing sugars. B cells mature in the _. Thymus. Estimation of reducing and Molecular weight of reducing sugars is relatively low. Note that, polysaccharides such as starch are non-reducing sugars. Non-reducing sugar does not have a free aldehyde or ketone group. Some disaccharides have exposed carbonyl groups and are also reducing sugars. The anomeric carbon is that which is derived from the carbonyl group and contains two oxygen substituents. Content provided and moderated by BiologyOnline Editors. ' Why do academics stay as adjuncts for years rather than move around? Reducing Sugar | bartleby To subscribe to this RSS feed, copy and paste this URL into your RSS reader. They give positive result with Tollens test. Why is maltose a reducing sugar but not sucrose, even though they're both disaccharides? In base, H on C2 may be removed to form enolate ion. If a law is new but its interpretation is vague, can the courts directly ask the drafters the intent and official interpretation of their law? Reducing sugar is any carbohydrate which is capable of being oxidized and causes the reduction of other substances without having to be hydrolyzed first. They are all artistically enhanced with visually stunning color, shadow and lighting effects. Carbohydrate which does not contains free aldehyde and ketone group is known as non-reducing sugars. Although caramelization can occur at milder temperatures, it is favored at temperatures higher than 120C. Madurai. There are several reasonable mechanisms for these conversions and we will not look at them in detail. The characterization of sugars as reducing or non-reducing is gives useful clues as to their structures. Non-reducing sugars are either dimers, trimers, or polymers, which are formed of many reducing monomeric units by the formation of a glycosidic bond. Reducing sugars produce mutarotation form osazones. In this case there is no hemiacetal functional group, so fructose is a non-reducing sugar. Such as: Some disaccharides are also reducing sugars such as lactose. Reducing sugar definition and example, non-reducing sugar definition and example, Estimation of reducing sugar by DNSA method, Estimation of total sugars by anthrone metod, Estimation of non-reducing sugar from amount of total sugars and reducing sugar, formula for estimation of non-reduci. In the food industry, the level of reduced sugars decides their quality. When heated, they melt and form a fluid which sets into a hard mass on cooling. Register TODAY for the 10th Annual Run Of The Dead. Reducing sugars have the ability to donate electrons. At 2 y a high relative intake of sugar and fat was associated with a low energy intake and a large weight reduction in the gastroplasty group. Reducing and Non Reducing Sugars - YouTube 0:00 / 6:20 Reducing and Non Reducing Sugars Aasoka 156K subscribers 139K views 4 years ago Science Videos | Learn with AASOKA Aasoka presents a. (test for sugars having free carbonyl groups. Reducing sugars have a sweet taste. Reducing sugars give a dark-red color (brick color) when they react with Benedict's solution. They lack ability to reduce cupric ions of Benedicts solution to coprous ions. Xylose can be utilized as a sweetener in the form of . Epimerization. Non-reducing sugar does not reduce Fehling's solution and Tollens reagent. What are five examples of non-reducing sugars? It has millions of presentations already uploaded and available with 1,000s more being uploaded by its users every day. Non-reducing sugars give a negative Fehlings test. In amylopectin, another type of starch, there are branches which involve acetal linkages through the oxygen on carbon 6. Here is an example from Wikipedia, it is Maltose, the same as your third compound. How do you identify reducing / non-reducing sugar by looking at structure? Strong oxidizing agents like Conc nitric acid yields dicarboxylic acid Saccharic acid. Calculation of Sugar Acid ratio of some fruits. Maltose is a reducing sugar, while sucrose is a non-reducing sugar. Research Institute, All polysaccharides are non-reducing sugars, and so are most disaccharides and oligosaccharides. ???????? Reducing sugar are a good reducing agent. This is done by the enzymes called glycosidases which are found in saliva. Quantitative identification of glucose using DNSA with spectroscopy. PRS. If we look at this in the context of the use of these materials in a plant, starch is found as a storage medium for glucose in seeds and tubers. Whats the grammar of "For those whose stories they are"? Test to distinguish reducing vs non-reducing sugars, Electron Configuration: The Key to Chemical Reactivity, Braggs Law [n = 2d sin]: A Relationship Between (d & ), Memorizing the Periodic Table: 3 Easy & Proven Ways, Neutralization Reactions: The Acid Base Balancing, Sugars that have a free aldehyde or ketone group and can reduce other compounds, Sugars that do not have a free aldehyde or ketone group and cannot reduce other compounds, Common Examples: glucose, fructose, maltose, Common Examples: sucrose, lactose, cellulose, Positive result with Tollen's reagent (forms a silver mirror), Negative result with Tollen's reagent (no reaction), Color changes are observed in Benedict test, They can be used as precursors in millard reaction. Stack Exchange network consists of 181 Q&A communities including Stack Overflow, the largest, most trusted online community for developers to learn, share their knowledge, and build their careers. Non-reducing lack ability to reduce cupric ions of Benedicts solution to coprous ions. Author: Maryam Kheirkhah Last modified by: USER-1 Created Date: 11/7/2004 6:21:42 AM Document presentation format: On-screen Show, | PowerPoint PPT presentation | free to view. The cellulose produced as the plant grows is a major structural component of the plant. Reducing sugars give a positive Fehlings test. Weve updated our privacy policy so that we are compliant with changing global privacy regulations and to provide you with insight into the limited ways in which we use your data. All common monosaccharides are reducing sugars. Once you realize that a hemiacetal can equilibrate with a carbonyl (e.g. Molecular weight of reducing sugars is relatively low. Connect and share knowledge within a single location that is structured and easy to search. The disaccharide sucrose is a non-reducing sugar. Activate your 30 day free trialto unlock unlimited reading. DETECTION OF PARAMETERS AND ACTIVE COMPONENTS IN HONEY, Alja pec and Ivana General analytical methods of milk powder final, CHEMICAL TEST & IMPORTANCE OF CARBOHYDRATES. Chemical properties of natural colors, chlorophyll, carotenoids, anthocyanins Estimation of Carbohydrates by anthrone method, Estimation of reducing and non reducing sugar, General analytical methods of milk powder final, Isolation, industrial production of phytoconstituents by Pooja Khanpara, Isolation, identification & estimation by Pooja Khanpara, Determination of Starch Damage of Sample Flour. 9 Difference between Reducing and Non-Reducing Sugar (With Table) Reducing sugar is a type of sugar that consists of a free aldehyde group or a free ketone group, allowing the molecule to act as a reducing agent. Glucose is the most abundant monosaccharide on the plant, which is primarily produced by green algae and plants. We've updated our privacy policy. It is in equilibrium with any acyclic aldehyde. Sucrose, starch, inositol gives a negative result, whereas lactose and maltose give a positive result with benedict's test. Our new CrystalGraphics Chart and Diagram Slides for PowerPoint is a collection of over 1000 impressively designed data-driven chart and editable diagram s guaranteed to impress any audience. reducing and non reducing sugars slideshare. The term sugar related to total sugar, reducing sugar and non reducing sugar. Avg rating:3.0/5.0. Fructose is a reducing sugar. PDF Biochemistry LD - LD Didactic To detect the presence of carbohydrates in a solution. Reducing and non-reducing sugar - Introduction o Reducing sugar: Sugar that can act as a reducing agent due to the presence of free aldehyde or ketone groups o Non-Reducing Sugar: Sugar which does not have free aldehyde or ketone functional group is the non- reducing sugar. Tests of Carbohydrates - Chemistry Practicals Class 12 - BYJUS It is used as a source of glucose both for energy and as a raw material for cellulose as the plant sprouts and enters its initial growth period. Hemicellulose can be hydrolyzed to pentose sugar, with the help of several hemicellulolytic enzymes. Reducing sugar has a free aldehyde (-CHO) or ketonic (-CO) group. Weve updated our privacy policy so that we are compliant with changing global privacy regulations and to provide you with insight into the limited ways in which we use your data. Non-reducing sugar generally has a less sweet taste. Does a summoned creature play immediately after being summoned by a ready action? when a guy calls you bacha the wrong missy hellstar quotes burke united methodist church calendar. - Medical Biochemistry Molecular Principles of Structural Organization of Cells CARBOHYDRATES CARBOHYDRATES Are hydrated carbon molecules [CnH2nOn or (CH2O)n - Erythro and Threo. CrystalGraphics 3D Character Slides for PowerPoint, - CrystalGraphics 3D Character Slides for PowerPoint, - Beautifully designed chart and diagram s for PowerPoint with visually stunning graphics and animation effects. In the highest quartile of mono+disaccharide intake (> 142 g) weight loss was 29.9 kg compared to 25.1 kg in lowest quartile (> 72 g). They can donate electrons to other compounds and cause the reduction of other compounds. In isomaltose, the glucose units are held together by o (1 . Can you write oxidation states with negative Roman numerals? Last time we explored the structural characteristics of monosaccharides. This means that the cyclic hemiacetal form of a sugar will produce an equilibrium amount of the open-chain aldehyde form, which will then reduce the copper(II) to copper (I) and give a positive test. 7. They give a positive reaction towards the Fehlings test. They can reduce other compounds. Why are polysaccharides non-reducing sugars? The linkages between the monosaccharide ring units in disaccharides are acetal linkages. If the red color precipitates are formed, it confirms the presence of reducing sugars. A sugar without a hemiacetal is a non-reducing sugar. Activate your 30 day free trialto continue reading. AMERICAN GARDENER shall not be responsible for any loss of profit, indirect, incidental, special, or consequential damages arising out of the use of the data and information derived from this web site. Comparision Reducing sugars have access to their open chain form. Alle links, video's en afbeeldingen zijn afkomstig van derden. It is in hemiacetal or hemiketal form whereas non-reducing form is in acetal or ketal form. The reactants are reducing sugar and amines in the Maillard reactions, whereas only sugar, reducing or nonreducing, is the reactant of caramelization. - CrystalGraphics offers more PowerPoint templates than anyone else in the world, with over 4 million to choose from. Learn Reducing and Non - Reducing Sugars in 3 minutes. - Toppr Reducing sugars include all monosaccharides and some disaccharides. Is it correct to use "the" before "materials used in making buildings are"? The linkage between the glucose and fructose units in sucrose, which involves aldehyde and ketone groups, is responsible for the inability of sucrose to act as a reducing sugar. The term "catalyzed" implies that enzyme speeds up the reaction in both directions, so that both formation and hydrolysis (conversion from acetal to hemiacetal using a molecule of water) are faster with the enzyme. And, best of all, it is completely free and easy to use. Collect the supernatant and evaporate it by keeping it on a water bath at 80C. It is important to note that the reducing sugars can be identified by different tests like benedicts test and fehling solution test. Examples of reducing sugars are all monosaccharides and some disaccharides, some oligosaccharides, and some polysaccharides. Notes. Nonreducing sugar A sugar that cannot donate electrons to other molecules and therefore cannot act as a reducing agent. Some commonly encountered examples of reducing sugars are glucose, fructose, galactose, ribose, etc. It only takes a minute to sign up. Reducing sugars are sugars where the anomeric carbon has an OH group attached that can reduce other compounds. The sugar content in a food sample is estimated by determining the volume of the unknown sugar solution . Test Your Knowledge On Tests Of Carbohydrates! This is because it contains a free ketone group. In contrast, most polysaccharides are non-reducing sugars. Aldehydes are fairly easy to oxidize to carboxylic acids, while acetals (which have no carbonyl group) are quite difficult to oxidize. document.getElementById( "ak_js_1" ).setAttribute( "value", ( new Date() ).getTime() ); Anupama Sapkota has a B.Sc. Non-Reducing Sugar Sugar which does not have free aldehyde or ketone functional group is the non-reducing sugar. Slides: 8. Jasmine Juliet .R This brings us to the topic of disaccharides. When it is a sugar alcohol, for example in 'sugar-free' gum Sucrose is called a nonreducing sugar because it does not react Chapter 7.1: Monosaccharides and Disaccharides. Sucrose is a glucose carbon connected at the anomeric carbon to a fructose carbon. The cellulose act as the raw material for the formation of the cellulose acetate. Estimation of reducing and nonreducing sugars. If the sugar used is glucose, they are "glucosides." Can I tell police to wait and call a lawyer when served with a search warrant? Reducing form of glucose (the aldehyde group is on the far right) A reducing sugar is any sugar that is capable of acting as a reducing agent. Is galactose a reducing sugar? Reducing suar, non reducing sugar introduction, examples, extraction from plant sample, estimation of reducing sugar, estimation of total sugar, detected value applied in formulas, result. SDS-page non-reducing (w/o B-ME): S-S are intact but protein is denatured. 19. rev2023.3.3.43278. Some disaccharides and all polysaccharides are non-reducing sugars. It is important to note that the reducing sugars can be identified by different tests like benedict's test and fehling solution test. Non-Reducing Sugars. The reducing sugars can form osazone by reacting with phenylhydrazine. Learn more about Stack Overflow the company, and our products. Since our glycosidases are unable to hydrolyze the beta linkages in cellulose, we cannot digest cellulose, even though it is also a polymer of glucose. Laney Grey Seduces Closeted Lesbian Into Sex! Sucrose, starch, inositol gives a negative result, whereas lactose and maltose give a positive result with benedict's test. The reducing sugar reduces the copper (III) ions in these tests into copper (I) ions resulting in the formation of a brick-red copper oxide precipitate. Classification of compounds into reducing and non-reducing sugars. All monosaccharides and some disaccharides are examples of reducing sugars. Comprehensive Chemistry, Part 2. The disaccharide sucrose is a non-reducing sugar. PRIVATE com Perky Tits Candie Luciani Shoves Wide Dick Up Her Butthole! We can differentiate between reducing and non-reducing sugars by the following test: In this test, first, we take the food sample. coach house furniture stockists near me.
In contrast, acetal forms (glycosides) are not reducing sugars, since with base present, the acetal linkage is stable and is not converted to the aldehyde or hemiacetal. Non-reducing sugars have a higher molecular weight as they are usually of a larger size. The conversion between an aldehyde and a hemiacetal is catalyzed either by base or by acid. Whereas non-reducing sugars do not show this property. The sugar type that exhibits its property as a reducing agent as it consists of free ketone and aldehyde functional groups is termed reducing sugars. non-reducing sugar Glycogen is even more highly branched than amylopectin. - Chemistry . The test is based on the principle of reduction of copper sulfate into copper oxide, which results in the formation of a red brick precipitate. Compound b constitutes a glycoside which is an acetal. whatever happened to matthew simmons. All monosaccharides are reducing sugars. BOBSTGIRLS: The most perfect and precious ass that you will be able to see for a long time, Valencia the Tgirl of the year, My tinder date and I went to a hotel and fucked until we both cum, AMATEUR EURO Amateur Lady Mia Wallace Gets Cock In Her Ass And Pussy In Public. Performance & security by Cloudflare. How to Name Alkenes? - Carbs. Non-reducing sugars are poor, reducing agents. Examples of non-reducing sugars include: Sucrose Trehalose Raffinose Gentiarose Melezitose Stachyose Verbascose Sucrose is the most commonly known non-reducing sugar. Clipping is a handy way to collect important slides you want to go back to later. Analysis of analgesics and antipyretics.indu, ANALYSIS OF FERMENTATION PRODUCTS BY HIMAJA, Download-manuals-water quality-technicalpapers-standardanalyticalprocedures, Estimation of Carbohydrates by anthrone method. Estimation of reducing and non reducing sugar - SlideShare Agricultural College Such beta linkages are found in cellulose. Sucrose is their most common source. (PDF) Effect of Spacing and Varieties on Quality Parameters of Rabi You can read the details below. Non-reducing sugars have aldehyde and ketone groups, but they are involved in the cyclic form of the sugar molecule. Reducing And Non Reducing Sugar Video Lecture from Biomolecules Chapter of Chemistry Class 12 for HSC, IIT JEE, CBSE & NEET.Android Application - https://pla. Reduction is the chemists term for electron gain, A molecule that gains an electron is thus, A molecule that donates electrons is called a, A sugar that donates electrons is called a, The electron is donated by the carbonyl group, Benedicts reagent changes colour when exposed to, Benedicts reagent undergoes a complex colour, The carbonyl group is free in the straight, BUT remember the ring form and the straight, So all monosaccharides are reducing sugars, All monosaccharides reduce Benedicts reagent, In some disaccharides e.g. Alle rechten voorbehouden. B. Pharm. Starch is a non-reducing sugar as it doesnt have a free aldehyde or ketone group present in the structure. If we apply this feature of the scheme to a solution of glucose in methanol (with a trace of acid catalyst included), we get: The acetal products are called "glycosides." Oxidation and Reduction - Image Source: Savemyexams "After the incident", I started to be more careful not to trip over things. Ophthalmic Compositions and Methods for Reducing Oxidative Damage to An Biochemistry Addition of new glucose molecules occurs at the nonreducing ends, and these same ends, in the completed glycogen molecule, are attacked to liberate glucose-1-phosphate . We'll find that these acetal linkages are what holds di- and polysaccharides together. reducing and non reducing sugars slideshare. analysis of reducing sugars april 16th, 2019 - analysis of reducing sugars background sugars are members of the carbohydrate family examples include glucose fructose and sucrose some sugars can act as reducing agents and these sugars will contain an aldehyde functional group this property can be used as a basis for the analysis of reducing sugars Non-reducing sugars have aldehyde and ketone groups, but they are involved in the cyclic form of the sugar molecule. Fructose provides an example of a disaccharide in which the acetal linkage joins the anomeric carbons of a glucose molecule to the anomeric carbon of a fructose molecule. Maltose and lactose are reducing sugars, while sucrose . reducing and non reducing sugars slideshare. a. Is xylose a reducing sugar? The Fehling's Test measures how much copper can be reduced by a solution to determine how much reducing sugars are present. A procedure is described for the extraction of sucrose, glucose and fructose from storage root vegetables. how to add a lean to onto a metal building; kerry funeral home almonte; capital chemist bathurst Reducing and Non Reducing Sugars - YouTube - Glucose is the major biological fuel. Clipping is a handy way to collect important slides you want to go back to later. Reducing and NonReducing Sugars. Whatever your area of interest, here youll be able to find and view presentations youll love and possibly download. Reducing & Non-Reducing Sugars Sugars can be classified as reducing or non-reducing; this classification is dependent on their ability to donate electrons Reducing sugars can donate electrons (the carbonyl group becomes oxidised ), the sugars become the reducing agent The oxidizing agents used in carbohydrate chemistry are typically copper(II) compounds which are reduced to copper(I) oxide. how to dissolve pelvic adhesions without surgery. reducing and non reducing sugars slideshare. I fail to see carbonyl group here, How can I identify reducing / non-reducing sugar by looking at structure in picture? We've encountered a problem, please try again. Type II Diabetes Carbohydrates role in blood glucose Glycemic Index Glycemic Index Factors Influencing GI Carbohydrates and - Title: Diapositiva 1 Author: FRANCISCO Last modified by: Emma Created Date: 12/6/2009 5:00:45 PM Document presentation format: A4 (210 x 297 mm) Other titles, Chapter 23 Carbohydrates and Nucleic Acids. Organic Chemistry - A "Carbonyl Early" Approach (McMichael), { "1.01:_Carbonyl_Group-_Notation_Structure_Bonding" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.02:_Functional_Groups_Hybridization_Naming" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.03:_Additions-_Electrophilic_and_Nucleophilic" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.04:_Acetal_Formation_Mechanism_Resonance" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.05:_Nitrogen_Nucleophiles_-_Imine_Formation" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.06:_Addition_of_Organometallics_-_Grignard" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.07:_Oxidation_and_Reduction_alpha-C-H_acidity" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.08:_Enolates_Aldol_Condensation_Synthesis" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.09:_Carboxylic_Acid_Derivatives-_Interconversion" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.10:_Carboxylic_Acid_Derivatives_-_Alpha_Carbon_Reactions" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.11:_Fats_Fatty_Acids_Detergents" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.12:_Carboxylic_Acids" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.13:_Alcohols" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.14:_Ethers_Epoxides_Thiols" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.15:_Chirality_Three_Dimensional_Structure" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.16:_R_S_Naming_Two_or_More_Stereogenic_Centers" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.17:_Carbohydrates-_Monosaccharides" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.18:_Glycosides_Disaccharides_Polysaccharides" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.19:_Amines-_Structure_and_Synthesis" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.20:_Amines-_Reactions" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.21:_Amino_Acids_and_Peptides" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.22:_Proteins" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.23:_Nucleic_Acids" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.24:_Nucleophilic_Substitution_SN2_SN1" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.25:_Elimination_-_E2_and_E1" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.26:_Alkenes_and_Alkyne_Structure" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.27:_Electrophilic_Additions" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.28:_Polymers" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.29:_Metabolic_Organic_Reactions" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.30:_Aromatic_Compounds" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.31:_Electrophilic_Substitution" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.32:_Side_Chain_Oxidations_Phenols_Arylamines" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "1.33:_Radical_Reactions" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()" }, { "00:_Front_Matter" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "01:_Chapters" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", "zz:_Back_Matter" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()" }, 1.18: Glycosides, Disaccharides, Polysaccharides, [ "article:topic", "Reducing Sugars", "showtoc:no", "license:ccbyncsa", "licenseversion:40", "authorname:kmcmichael" ], https://chem.libretexts.org/@app/auth/3/login?returnto=https%3A%2F%2Fchem.libretexts.org%2FBookshelves%2FOrganic_Chemistry%2FBook%253A_Organic_Chemistry_-_A_Carbonyl_Early_Approach_(McMichael)%2F01%253A_Chapters%2F1.18%253A_Glycosides_Disaccharides_Polysaccharides, \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}}}\) \( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash{#1}}} \)\(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\) \(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\)\(\newcommand{\AA}{\unicode[.8,0]{x212B}}\), status page at https://status.libretexts.org.

What Was The Unforeseen Impact Of Forcing Weegy, Cardinals Front Office, Church Of 8 Wheels Closing, Is Sarah Marshall Related To Arthur Blank, Articles R