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MessagePosté le: Sam 3 Sep - 22:43 (2016)    Sujet du message: Summary Of All Organic Chemistry Reactions Pdf Download Répondre en citant




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Summary Of All Organic Chemistry Reactions Pdf Download

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Younah I dont know how much I can say thank you. Home Blog Online Tutoring Reaction Guide Study Guides Contact Feedback Mission Members Login Reaction Guide MOC Elite Master Organic Chemistry New? Start Here Study And Exam Tips Organic 1 Index Organic 2 Index Free Cheat Sheets Feedback Summary Sheets Summary Sheet: Functional Groups August 21, 2012 I thought it would be good to make a summary sheet based on functional groups, so here one is: Functional Group Summary Sheet (PDF) You can find other sheets in the Summary Sheets section of this site. All rights reserved Organic Chemistry Is Awesome About JamesAccountAdvanced Substitution Topics Sun Nov 10Alkene Mini Course Thanks!Alkene Mini-CourseAlkene WebinarAlkenes: Common Exam Problems (With Solutions)Alkyne Webinar Sun Dec 15 at 9pm ESTAlkynes Are A Blank CanvasBlogCancel SubscriptionCarbon Carbon BondsCommon Mistakes In Organic Chemistry: Pentavalent CarbonConfirming your email address&Crash Course On AlkenesCrash Course On Alkenes CheckoutDashboardDont Be Futyl, Learn The ButylsElimination Webinar Sunday Nov 24 at 9pm ESTFeedbackForm Styling Sandbox PageFrom Gen Chem To Organic ChemGetting StartedHomeHome-2How To Draw A Cyclohexane ChairHow To Succeed In Organic ChemistryHow To Succeed In Organic ChemistryInitiation, Propagation, TerminationInterviewIntroduction To Spectroscopy Seminar (Including NMR)Introduction To Substitution Webinar Tuesday Nov 5Leah Nomenclature Guest PostManage SubscriptionMembers LoginMissionMOC EliteMy Organic Chemistry Story Whats Yours?New Acid-Base WebinarNEW! Reagents AppOctober 22 Acid-Base WebinarOnline Organic Chemistry TutoringOrg 2 Post IndexOrganic 1Organic 2Organic Chemistry Study AdvicePost IndexPost Index 2Post Index Draftpost index draft 2ProductsOrganic Chemistry Reagent GuideReaction Guide1,4-addition of enolates to enones (The Michael Reaction)1,4-addition of nucleophiles to enones1,4-addition of organocuprates (Gilman reagents) to enonesAcidic cleavage of ethers (SN2)Addition Of Alcohols To Alkenes With AcidAddition of aqueous acid to alkenes to give alcoholsAddition of Dichlorocarbene to alkenes to give dichlorocyclopropanesAddition of dichloromethylene carbene to alkenesAddition of Grignard reagents to aldehydes to give secondary alcoholsAddition of Grignard reagents to esters to give tertiary alcoholsAddition of Grignard reagents to formaldehyde to give primary alcoholsAddition of Grignard reagents to ketones to give tertiary alcoholsAddition of Grignard reagents to nitriles to give ketones (after hydrolysis)Addition of HBr once to alkynes to give alkenyl bromidesAddition of HBr to AlkenesAddition of HBr twice to alkynes to give geminal dibromidesAddition of HCl once to alkynes to give alkenyl chloridesAddition of HCl to Alkenes to Give Alkyl ChloridesAddition of HCl to alkynes twice to give geminal dichloridesAddition of HI once to alkynes to give alkenyl iodidesAddition of HI twice to alkynes to give geminal diiodidesAddition of Hydroiodic Acid to Alkenes to Give Alkyl IodidesAddition of LiAlH4 to aldehydes to give primary alcoholsAddition of LiAlH4 to ketones to give secondary alcoholsAddition of NaBH4 to aldehydes to give primary alcoholsAddition of NaBH4 to ketones to give secondary alcoholsAddition of organocuprates (Gilman reagents) to acid chlorides to give ketonesAddition to alkenes accompanied by 1,2-alkyl shiftAdditions to alkenes accompanied by 1,2-hydride shiftsAldol addition reaction of aldehydes and ketonesAldol CondensationAlkylation of enamines with alkyl halidesAlkylation of enolatesAllylic bromination of alkanes using NBSBaeyer-Villiger ReactionBase-promoted formation of enolates from ketonesBasic hydrolysis of esters (saponification)Beckmann RearrangementBromination of alkenes with Br2 to give dibromidesBromination of aromatic alkanes to give alkyl bromidesBromination of Aromatics to give BromoarenesCannizarro ReactionChlorination of alkenes with Cl2 to give vicinal dichloridesChlorination of Arenes to give ChloroarenesClaisen Condensation of estersCleavage of ethers using acid (SN1 reaction)Clemmensen Reduction of Ketones/Aldehydes to AlkanesConversion of acid chlorides to aldehydes using LiAlH(O-tBu)3Conversion of acid chlorides to esters through addition of an alcoholConversion of alcohols to alkyl bromides using PBr3Conversion of alcohols to alkyl chlorides using SOCl2Conversion of alcohols to alkyl halides using HClConversion of Alkyl halides to ethers (SN1)Conversion of carboxylic acids into acid chlorides with SOCl2Conversion of carboxylic acids to carboxylates using baseConversion of carboxylic acids to esters using acid and alcohols (Fischer Esterification)Conversion of tertiary alcohols to alkyl bromides using HBrConversion of tertiary alcohols to alkyl iodides with HIConversion of thioacetals to alkanes using Raney NickelCurtius Rearrangement of Acyl Azides to IsocyanatesDecarboxylation of beta-keto carboxylic acidsDehydration of amides to give nitrilesDeprotonation of alcohols to give alkoxidesDeprotonation of alkynes with base to give acetylide ionsDiels Alder Reaction of dienes and dienophilesDihydroxylation of Alkenes to give 1,2-diols (vicinal diols)Dihydroxylation of alkenes with cold, dilute KMnO4 to give vicinal diolsElimination (E1) of alkyl halides to form alkenesElimination (E1) with 1,2-alkyl shiftElimination (E1) with hydride shiftElimination (E2) of alkyl halides to give alkenesElimination of alcohols to give alkenes using POCl3Elimination of water from alcohols to form alkenes using acidEnamine HydrolysisFormation of Acetals from Aldehydes and KetonesFormation of alkynes through double elimination of vicinal dibromidesFormation of amides from acid chlorides and aminesFormation of Amides Using DCCFormation of anhydrides from acid halides and carboxylatesFormation of Bromohydrins from alkenes using water and Br2Formation of bromohydrins from alkenes using water and NBSFormation of Carboxylic Acids from Acyl ChloridesFormation of carboxylic acids from Grignard reagents and CO2Formation of chlorohydrins from alkenes using water and Cl2Formation of Cyanohydrins from ketones and aldehydesFormation of cyclopropanes from alkenes using methylene carbene (:CH2)Formation of Diazonium Salts from Aromatic AminesFormation of enamines from ketones/aldehydes and secondary aminesFormation of epoxides from alkenes using m-CPBAFormation of epoxides from bromohydrinsFormation of Gilman reagents (organocuprates) from alkyl halidesFormation of Grignard Reagents from Alkenyl HalidesFormation of Grignard Reagents from Alkyl HalidesFormation of hydrates from aldehydes/ketones and H2OFormation of imines from primary amines and ketonesFormation of organolithium reagents from alkyl halidesFormation of thioacetals from aldehydes and ketonesFormation of tosylates from alcoholsFree Radical Addition of HBr To AlkenesFree Radical Bromination of AlkanesFree Radical Chlorination of AlkanesFriedel Crafts alkylation of arenesFriedel-Crafts acylation of aromatic groups to give ketonesHalogenation of AlkynesHell-Vollhard-Zelinsky ReactionHofmann elimination of alkylammonium salts to give alkenesHofmann Rearrangement of Amides to AminesHydroboration of AlkenesHydroboration of alkynes using BH3 to give aldehydesHydrogenation of Alkenes to give AlkanesHydrogenation of Alkynes to Alkanes using Pd/CHydrolysis of acetals to give aldehydes and ketonesHydrolysis of esters to carboxylic acids with aqueous acidHydrolysis of imines to give ketones (or aldehydes)Hydrolysis of nitriles with aqueous acid to give carboxylic acidsIodination of alkenes to give vicinal diiodides (1,2-diiodides)Iodination of Aromatics with I2Keto-enol tautomerismKiliani-Fischer SynthesisNitration of aromatic groupsNucleophilic Aromatic Substitution (SNAr)Nucleophilic Aromatic Substitution Via ArynesOpening of epoxides with acid and water to give trans diolsOpening of epoxides with nucleophiles under acidic conditionsOxidation of aldehydes to carboxylic acids using Cr(VI)Oxidation of aldehydes to carboxylic acids with Ag2OOxidation of aromatic alkanes with KMnO4 to give carboxylic acidsOxidation of primary alcohols to aldehydesOxidation of Primary Alcohols to Aldehydes using PCCOxidation of primary alcohols to carboxylic acidsOxidation of secondary alcohols to ketones using PCCOxidation of thiols to disulfidesOxidative cleavage of 1,2-diols to give aldehydes/ketonesOxidative cleavage of alkenes to give ketones/carboxylic acids using ozone (O3) (oxidative workup)Oxidative cleavage of alkenes to ketones/carboxylic acids using KMnO4Oxidative Cleavage of Alkynes with KMnO4Oxidative Cleavage of Alkynes with Ozone (O3)Oxymercuration of Alkenes to form Ethers using Hg(OAc)2Oxymercuration of AlkynesOxymercuration: Alcohols from alkenes using Hg(OAc)2 and WaterOzonolysis of alkenes to ketones and aldehydes (reductive workup)Partial reduction of alkynes to trans alkenes using sodium and ammoniaPartial reduction of alkynes with Lindlars catalyst to give cis alkenesPinacol RearrangementPolymerization of dienes with acidProtection of alcohols as silyl ethersProtonation of alcohols to give oxonium ionsProtonation of Grignard reagents to give alkanesReaction of alkyl halides with water to form alcohols (SN1)Reaction of epoxides with nucleophiles under basic conditionsReactions of Diazonium SaltsReduction of aromatic ketones to alkanes with Pd/C and hydrogenReduction of aromatic nitro groups to amino groupsReduction of carboxylic acids to primary alcohols using LiAlH4Reduction of esters to aldehydes using DIBALReduction of esters to primary alcohols using LiAlH4Reduction of nitriles to primary amines with LiAlH4Reductive AminationSharpless EpoxidationSN2 of Cyanide with Alkyl Halides to give NitrilesSN2 reaction between azide ion and alkyl halides to give alkyl azidesSN2 Reaction of Acetylide Ions with Alkyl HalidesSN2 reaction of alkoxide ions with alkyl halides to give ethers (Williamson synthesis)SN2 reaction of alkyl halides with hydroxide ions to give alcoholsSN2 reaction of amines with alkyl chlorides to give ammonium saltsSN2 reaction of carboxylate ions with alkyl halides to give estersSN2 reaction of hydrosulfide ion with alkyl halides to give thiolsSN2 reaction of organocuprates (Gilman reagents) with alkyl halides to give alkanesSN2 reaction of thiolates with alkyl halides to give thioethers (sulfides)SN2 reaction of water with alkyl halides to give alcoholsStille ReactionSubstitution (SN1) with hydride shiftSubstitution with accompanying alkyl shiftSulfonylation of Arenes to give sulfonic acidsSuzuki ReactionThe Gabriel synthesis of aminesThe haloform reaction: conversion of methyl ketones to carboxylic acidsThe Heck ReactionThe Malonic Ester SynthesisThe Mannich ReactionThe Robinson AnnulationTransesterification promoted by alkoxidesWittig Reaction conversion of ketones/aldehydes to alkenesWolff Kishner Reaction conversion of ketones/aldehydes to alkanesWolff RearrangementResource GuideResourcesShare Your Organic Chemistry StorySign Up For The Reaction GuideSign Up To Be A Flashcards Beta Tester!Signup for the Reaction GuideSomething Has Gone WrongSpectroscopy Video Thanks!Spectroscopy Video CheckoutStereochemistry Webinar Sunday Nov 3Store ActionStudy and Exam TipsSummary SheetsTest PagetesttypgThanks for Joining!Thanks! Youre signed up for the newsletter.Thanks! Youre Signed Up For The Reaction GuideThe Cat Line DiagramThe Web of ReactionsThoughts On O-ChemTips#9109 (no title)ConjugationInitial Tails and Final Heads3 Ways To Make OH A Better Leaving GroupA Simple Formula For 7 Important Aldehyde/Ketone ReactionsAcetoaceticAcids (Again!)Activating and DeactivatingActors In Every Acid Base ReactionAddition EliminationAddition Pattern 1 CarbocationsAddition pattern 2 3 membered ringsAddition ReactionsAlcohol Personality AdjustmentAldehydes And Ketones AdditionAlkene Pattern #3 The Concerted PathwayAlkyl RearrangementsAlkynes 3 PatternsAlkynes: Deprotonation and SN2AminesAromaticity: Lone PairsAvoid These Resonance MistakesBest Way To Form AminesBulky BasesCarbocation StabilityCarbocation Stability RevisitedCarboxylic Acids are AcidsChair FlipsCis and TransConformationsConjugate AdditionCurved Arrow RefresherCurved ArrowsDecarboxylationDetermining AromaticityDiels Alder Reaction 1Dipoles: Polar vs. Actually I am taking organic chemistry three times, and i hope it is my last attempt to pass orchem. 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james Im very happy you find it useful Sophie. Get The Latest Updates facebook twitter rss email Recent Posts Popular Posts Recent Comments Degrees of Unsaturation (Index of Hydrogen Deficiency)Posted on: Aug 26, 2016Structure Determination Case Study: Deer Tarsal Gland PheromonePosted on: Aug 23, 2016Natural Product Isolation (2) - Purification of Crude Mixtures OverviewPosted on: Aug 12, 2016Natural Product Isolation (1) - ExtractionPosted on: Jul 12, 2016Now Available - The Spectroscopy Pack (PDF)Posted on: Jul 07, 2016 What Makes A Good Nucleophile?72Five Key Factors That Influence Acidity703 Trends That Affect Boiling Points70Polar Protic? Polar Aprotic? Nonpolar? All About Solvents57Comparing the SN1 and SN2 Reactions54 Miosz said in Structure Determination Case Study: Deer Tarsal Gland Pheromone - Just WOW. Izzy Hi James! Do you have a summary sheet for SN2/E2-SN1/E1 reactions? james I do! but you have to join the mailing list to get it :-) Addie Thank you so much for putting these together, they are an easy way to clarify all the reactions and see them at once before the exam. After youve done organ… Tagged as: aldol, amines, carbonyls, claisen, enamines, enolates, studying, Summary Sheets, williamson Summary Sheet #2: Enols andEnolates April 14, 2010 Tagged as: aldehydes, enolates, enols, ketones, summaries, Summary Sheets, tautomerism, tautomers Page 1 of 2:12Next Sign Up To Get Weekly Organic Chemistry TipsAnd get the free "How To Succeed In Organic Chemistry" E-bookPlease enter your first name*Please enter your email* About Master Organic Chemistry Imagine having a comprehensive online guide to help you solve your own problems in organic chemistry. I feel like having a bonfire with my orgo book because it is totally useless compared to this website. Bernadette Hi Ashley! I love it!! GO GET EM!!! I am encouraged by your note, because Im 50 taking this O-Chem II. As for volatility, the HCl will react with solvent or water forming a conjugate acid (e.g. James is awesome and so I feel I can do it now!!! Good luck to you and feel free to write me if you feel like it Bernadettefullgmail.com Why are you taking it? Me? Im thinking of applying to med school if the divine will supply the funding!! Im hopeful!!! and working hard. →James said in Conversion of carboxylic acids to esters using acid and alcohols (Fischer Esterification) - HCl can be used.

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