The aldehyde is not losing electrons to oxygen. It is a mild oxidative agent. Ketones do not give this test. Thanks for contributing an answer to Chemistry Stack Exchange! Potassium dichromate question Reactions for Carboxylic Acids and Ketones Reaction of Alcohols A2 chemistry Silvor mirror test . This precipitate dissolves in aqueous ammonia, forming the diamminesilver (I) ion, [Ag (NH3)2]+. We also acknowledge previous National Science Foundation support under grant numbers 1246120, 1525057, and 1413739. Tollens' reagent is an alkaline solution of ammoniacal silver nitrate and is used to test for aldehydes. Tollens' test chemical reaction . This is the balanced equation: $\ce{R-CHO + 2[Ag(NH3)2]+ + 3HO- -> R-COO- + 2Ag + 2H2O + 4NH3}$. Illustrated Glossary of Organic Chemistry - Tollens' test; Tollen's reagent Connect and share knowledge within a single location that is structured and easy to search. Does benzaldehyde give tollen's test? Explained by FAQ Blog Would acetone give a positive tollens test? - sisi.vhfdental.com Solution. This page titled Tollens Reagent is shared under a All Rights Reserved (used with permission) license and was authored, remixed, and/or curated by Gamini Gunawardena via source content that was edited to the style and standards of the LibreTexts platform; a detailed edit history is available upon request. Tollens reagent consists of silver nitrate(AgNO3), ammonia(NH3), and sodium hydroxide(NaOH). What is/has been the obstruction to resurrecting the Iran nuclear deal exactly as it was agreed under the Obama administration? Tollens' test - ECHEMI . An example of a positive Tollen s test is in Figure 10-33. Tollens' test, also known as a silver-mirror test, is a qualitative laboratory test that is used to differentiate between an aldehyde and a ketone. Reaction. Although Tollens' test, carried out in a Ag + NH 3 system, has been used for over hundred years for detecting aldehydes by the silver mirror reaction, the test becomes more sensitive by . 3) The freeing of one $\ce{O^2-}$ yields the hydrogen proton, $\ce{H+}$. You will never form oxygen dianion in an aqueous solution. (OH)2 + Ag+ &-> R-COOH + H+ + Ag^0} A terminal -hydroxy ketone gives a positive . Aqueous silver Ions are being reduced to silver metal onto a large glass Florence flask. Does tartaric acid give tollens test? - Sage-Answer Take 1 ml of a given sample in a clean, dry test tube. Zero Inflated Logistic Regression - Does This Exist? Iodine Test: Description, Principle, Procedure And Result Examples of Tollens' Test It takes advantage of the fact that aldehydes are oxidized readily, while ketones are not. Reducing sugars are sugars that have an aldehyde ending on the sugar that can be further oxidized into a carboxylic acid. It exploits the fact . This test is also called the silver mirror test based on the end product of this test. . Using Tollens' reagent (the silver mirror test) Tollens' reagent contains the diamminesilver (I) ion, [Ag (NH 3) 2] +. MathJax reference. 1. Gentle heating can be employed if no reaction is immediately observed. rev2022.11.22.43050. Tollens' Reagent - Chemistry LibreTexts 4) The above explains the hard stuff. The best answers are voted up and rise to the top, Not the answer you're looking for? (OH)O- + H2O + Ag^0} \\ Procedure of Tollens' test Take two clean, dry test tubes and add 1 ml of the test sample in one test tube and 1 ml of distilled water in another as blank. It is also known as silver mirror test since free silver metal is formed at the end of this test reaction. Do all aldehydes give tollen's test? Explained by FAQ Blog So the aldehyde gets oxidized to a carboxylic acid, and the OH remains untouched. Allow the test tubes to cool completely before examining the colour in both of them. It is prepared freshly in the laboratory. Browse other questions tagged, Start here for a quick overview of the site, Detailed answers to any questions you might have, Discuss the workings and policies of this site, Learn more about Stack Overflow the company. Fehling's solution is used as a chemical test used to differentiate between water-soluble aldehyde and ketone functional groups, and as a test for monosaccharides.The test was developed by German chemist Hermann von Fehling in 1849. The test is used to differentiate between reducing sugars and non-reducing sugars. Tollens' reagent is always used to distinguish between aldehyde and ketone functional groups. Your email address will not be published. By clicking Post Your Answer, you agree to our terms of service, privacy policy and cookie policy. This test cannot distinguish between an aldehyde and an -hydroxy ketone (e.g., hydroxy acetone) [1-4]. The complex now formed is known as the Tollens reagent. Tollens' test : r/chemistry - reddit 7. The history of this reaction goes back to 1882 when a work done by German chemist Bernard Tollens was published in a German journal. Is there any evidence from previous missions to asteroids that said asteroids have minable minerals? How alpha hydroxy ketone tollens test? Explained by FAQ Blog Aldehydes reacted with Tollen s reagent to deposit silver metal on the walls of the reaction vessel, forming a mirror. This is due to the fact that Tollen's reagent reacts with an acidic hydrogen forming a precipitate . \ce{R-C^. 5. Add 2.8% ammonia . Hence this option is correct. Next, freshly prepared Tollens reagent is added to the solution and it is warmed in a hot water bath. The preparation of Tollens reagent takes two steps. What could a technologically lesser civilization sell to a more technologically advanced one? As mentioned in the article, the test is used to differentiate between an aldehyde and a ketone. Tollen's reagent is a colorless, basic, aqueous solution containing silver ions complexed with ammonia, NH 3, [Ag(NH 3) 2 . Oxidation: Tollen's & Fehling's Reagent, BaeyerVilliger Oxidation, Videos This solution is sometimes called Tollens' reagent. Reaction of secondary alcohol with ammoniacal silver nitrate (Tollens Specifically, the carbon in the aldehyde is being oxidized; it is losing electrons to silver. Test Reagent Organic question show 10 more . I am trying to find a mechanism for the this reaction online, but the only thing I can find is the balanced equation. A gem-diol like intermediate is formed via a hydrogen shift, which then continues on to the final carboxylate anion. Tollens' Test- Definition, Principle, Procedure, Result, Uses It only takes a minute to sign up. Tollen's test is a chemical test used to distinguish reducing sugars from non-reducing sugars. Tollens' Test: Definition, Example, and Mechanism - Chemistry Learner Tollens' reagent 2 OH {\displaystyle {\ce {Ag 2OH))} Periodic Trends Ionization Energy Worksheets. Aldehyde reaction with Tollens reagent - Big Chemical Encyclopedia It is also known as silver mirror test since free silver metal is formed at the end of this test reaction. The following are true for Tollen's test, EXCEPT: It is otherwise known as the silver mirror test It is usually used to differentiate aldehydes from ketones Can be used as confirmatory test for citrates and tartrates It uses a reagent which is a colorless, basic, aqueous solution containing silver ions coordinated to ammonia [AgNH3)+2] Formation of metallic silver produces as black precipitate Thanks! To subscribe to this RSS feed, copy and paste this URL into your RSS reader. Tollens' test is a chemical test used to differentiate reducing sugars from non-reducing sugars. I am a 3rd-year student pursuing Int.MTech in CS and aspiring to be a data scientist.Being a JEE aspirant, I have gone through the pain of understanding concept the difficult way by going through various websites and material. Add about 2-3 drops of Barfoed's reagent to both the tubes and mix them in a vortex. Named after its German chemist discoverer, Bernhard Tollens, the Tollens' reagent test is used to identify aldehydes and their functional groups, as well as to distinguish between these and ketones.. Central to this test is the Tollens' reagent, which is composed of ammonia and silver nitrate, as well as sodium hydroxide, in order to stabilise the pH . To learn more, see our tips on writing great answers. Using these reactions we can now follow Fischer's train of logic in assigning the configuration of D-glucose. Tollens test is a qualitative laboratory test, used to distinguish between an aldehyde and a ketone. Ox-Aldehyd-T2.svg 318 57; 48 KB. Silver ions in the presence of hydroxide ions come out of solution as a brown precipitate of silver (I) oxide, Ag2O (s). Silver ions in the presence of hydroxide ions come out of solution as a brown precipitate of silver (I) oxide, Ag 2 O (s). When Tollens' reagent is gently warmed with a ketone, no silver mirror will be seen, as the ketone cannot be oxidised by Tollens' reagent, so no reaction takes place This is a negative test result The Ag+ ions in Tollens' reagent are oxidising agents, oxidising the aldehyde to a carboxylic acid and getting reduced themselves to silver atoms \end{align}$$. Legal. Observe the formation of color and note it down. Site design / logo 2022 Stack Exchange Inc; user contributions licensed under CC BY-SA. Test sample Materials required Test tubes Test tube stand Pipette Equipment Water bath Procedure of Tollens' test 11 Fascinating Chemistry Experiments (Compilation) 28 related questions found. It is based on the fact that aldehydes are readily oxidized whereas ketones are not. 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. What is the significance of the intersection in the analemma? Add 2 ml of Tollen's reagent to both the test tubes. Tollen's Test: Aldehydes give a positive silver mirror to Tollen's test while ketones give no reaction. Why is the silver salt ammoniated to form the Tollen's reagent? Propanal does not give iodoform test. The diamminesilver(I) complex is an oxidizing agent, which is itself reduced to silver metal, which in a clean glass reaction vessel forms a "silver mirror".This feature is used as a test for aldehydes, which are oxidized to carboxylic acids. \ce{RCHO + 3OH- &-> RCO2- + 2H2O + 2e-} The LibreTexts libraries are Powered by NICE CXone Expert and are supported by the Department of Education Open Textbook Pilot Project, the UC Davis Office of the Provost, the UC Davis Library, the California State University Affordable Learning Solutions Program, and Merlot. Step 2: Next, an adequate amount of aqueous ammonia is added to dissolve brown silver(I) oxide. Take control of 1 ml of distilled water in another tube. In the Tollens test one of the main components is tollens reagent. Though do have a look here, as you said, gentle heating is causing silver ppt to form, as. Tollens Reagent Silver Mirror Test for Aldehydes - Leah4sci It exploits the fact that aldehydes are readily oxidized (see oxidation), whereas ketones are not. The sugars react with alpha-naphthol in an acidic environment to form purple-colored furfural or hydroxymethylfurfural derivatives. The reaction that takes place during the Tollens' Test is as follows: RCHO + 2 (AG (NH3)2OH) + 2NaOH RCOONH4 + 3NH3 + 2Ag (s) + H2O (Aldehyde) (Tollens' reagent) (Carboxylic acid) (Elemental Silver) What is Tollens' Reagent? Ox-Aldehyd-T1.svg 671 130; 78 KB. Tollens Test - Formula, Preparation, Uses, FAQs - Careers360 Tollens reagent is a mild oxidizing chemical reagent that is used in the Tollens test. Ag2O + 4NH3 + 2NaOH + H2O 2[Ag(NH3)2]OH. Ox-Tollens.svg 788 130; 78 KB. Things to Remember on Tollens' Test Tollens' reagent is usually used as a test for aldehydes, with which it gives a characteristic silver mirror: It is often said that Tollens' reagent does not react with alcohols. 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MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Aromatic_Compound : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Aromatic_Ether : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Aromatic_Hydrocarbon : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Aromatic_Hydrogen : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Aryl_Carbanion : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Aryl_Carbocation : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Aryl_Ester : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Aryl_Group : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Aryl_Halide : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Aryl_Radical : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Aryne : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Assisted_Homolysis : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Asymmetric_Carbon_Atom : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Autoxidation : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Axial_Bond : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", A_Value : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", "Baeyer-Villiger_Oxidation" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Base : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Base_Peak : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Base_Strength : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Beckmann_Rearrangement : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", "Beer-Lambert_Law" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Benzene_Ring : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Benzilic_Acid_Rearrangement : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Benzylic_Carbocation : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Benzylic_Carbon : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Benzylic_Halide : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Benzylic_Radical : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Benzyl_Carbocation : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Benzyl_Radical : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Benzyne : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Benzyne_Mechanism : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Betaine : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Beta_Amino_Acid : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Beta_Anomer : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Beta_Carbon : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Beta_Cleavage : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Beta_Hydrogen : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Bicycloalkane : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Birch_Reduction : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Boat_Conformation : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Bond_Angle : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Bond_Axis : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Bond_Dissociation_Energy : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Branched_Alkane : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Bridge : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Bridged_Bicycloalkane : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Bridgehead_Carbon_Atom : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", "Brnsted-Lowry_Theory" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Bromohydrin : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", "C-Terminal" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", "Cahn-Ingold-Prelog_Convention" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carbanion : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carbanion_Equivalent : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carbene : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carbene_Equivalent : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carbenoid : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carbocation : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carbocation_Rearrangement : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carbocycle : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carbohydrate : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carbonyl_Carbon : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carbonyl_Compound : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carbonyl_Group : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carbonyl_Oxygen : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carboxylate_Ion : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carboxylation : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carboxylic_Acid : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carboxylic_Acid_Anhydride : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carboxylic_Acid_Derivative : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carboxylic_Acid_Ester : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carboxylic_Acid_Ester_Group : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carboxylic_Acid_Group : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Carboxylic_Acid_Salt : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Catalytic_Hydrogenation : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Catalytic_Reduction : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Center_of_Chirality : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", CFB : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Chair_Conformation : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Chemically_Equivalent_Ligands : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Chemical_Ionization : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Chemical_Shift : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Chemoselective : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Chirality_Center : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Chiral_Atom : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Chiral_Center : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Chiral_Molecule : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Chlorofluorocarbon : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Chlorohydrin : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Chromate_Ester : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Chromic_Acid : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", CIP_Convention : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", "Cis-Trans_Isomers" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Claisen_Condensation : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Claisen_Rearrangement : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Clemmensen_Reduction : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Combustion : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Concerted_Reaction : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Condensation_Reaction : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Configuration : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Conformation : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Conformer : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Conjugated_Diene : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Conjugated_Double_Bond : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Conjugate_Acid : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Conjugate_Addition : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Conjugate_Base : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Constitutionally_Heterotopic : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Constitutional_Isomers : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Coordination_Number : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Cope_Elimination : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Cope_Reaction : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Cope_Rearrangement : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Coupling : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Coupling_Constant : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Coupling_Reaction : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Crossed_Aldol_Condensation : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.b__1]()", Crossed_Aldol_Reaction : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass226_0.
