Enamine Study guides, Revision notes & Summaries

This is a detailed and comprehensive note on Enol Enolates and Enamines. * With formulas and we'll drawn structures "* You'll love it!

MCAT 101 EXAM 2 STUDY GUIDE 1. Explanation: This is an Analogy question. A: No. ...

Organic chemistry 2 exam preparation - information on nucleophilic addition reactions, water as nucleophile. alcohols as nucleophiles, hydrogen nucleophiles, oxygen nucleophiles. nitrogen nucleophiles, enamine formation, imines formation, hydrazone formation and reduction, cyanohydrin formation & reaction, Wittig reaction, Baeyer-Villiger oxidation, Carboxylic acid preparation and reactions, acid anhydride reactions, esters preparation, esters reactions, amide preparation, amide reactions, nitri...

All notes after exam 2 before exam 3. Hydration, acid-catalyzed acetal formation, hemiacetal, cyclic hemiacetal, imine, wolf-kishner, enamine, NaHH4-CH30H, cyanohydrin, nitrile reduction/hydrolysis, Wittig, ylide, bayer-villager, carboxylic acid, acid chloride, anhydride, ester, amide, fisher esterification, ester reactions, monomers, polymers, enols, aldol condensation.

- UBC CHEM 233 cheat sheet used on the 2022W1 final exam - Comprehensive, includes fischer and newman projections, ARIO, Sn1 and Sn2 reactions, oxidation state, hydrogenation, nucleophilic acyl substitution, carbohydrate cyclization, hydrolysis of enamine, imines and acetals/ketals

Exam (elaborations) TEST BANK FOR The Art of Writing Reasonable Organic Reaction Mechanisms 3rd Edition By Robert B. Grossman (Solution Manual) sp2 hybridization. One of the lone pairs is in a p orbital, and the other is in an sp2 orbital. Only the lone pair in the p orbital is used in resonance. 1.5. (a) No by-products. C(1–3) and C(6–9) are the keys to numbering. (b) After numbering the major product, C6 and Br25 are left over, so make a bond between them and call it the by-product....

Organic Chemistry 202 Synthetic Transformations, Top Exam Questions & answers, Rated A+ reduction of an aldehyde or ketone to an alcohol LiAlH4 or NaBH4 H3O H2O lithium dialkyl cuprate reagent from an alkyl halide 4 Li metal CuI reduction of a nitro group to an amine Zn(Hg) HCl reduction of a benzyl carbonyl H2/Pd or Zn(Hg) HCl NAS (normal condition must be 1 EWG ortho/para to leaving group) nucleophile (–OH, –OR, R3N) benzyne reactions 1) NaOH 2) dilute acid benzyne...

Summary of S3 - Catalytic Asymmetric Reactions 1. Introduction 2. Organocatalytic aldol reactions 3. Asymmetric Mannich, oxygenation and amination reactions 4. Other organocatalytic enamine reactions 5. Organocatalytic radical reactions 6. Asymmetric iminium ion catalysis 7. Catalytic asymmetric cycloaddition reactions 8. Asymmetric nucleophilic addition to aldehydes

Different Nitrogen names - ANSWER Enamine: C=C-N Amine : C-N Imine: C=N Amide: O=C-N Imide: O=C-N-C=O Ketone(aldehyde) + 1° amine --> Imine Ketone(aldehyde) + 2° amine ---> Enamine think about it when replace the Oxygen of carbonyl and attach NitrogenR, /Make sure It has a lone pair. for the 2 ° amine move double bond to the C. Amine - ANSWER C-N Myopia (nearsighted) - ANSWER *(-)F= diverging mirror /convex mirror/concave lens *convex mirror: image always virtual...

This document contains digitally taken, handwritten notes for the reactions of aldehydes and ketones. It covers information including nomenclature, synthesis and reactions with strong and weak nucleophiles. It also shows how to make hemi-acetals and acetals. Other reactions include the Wittig reaction and how to synthesize and Ylide. Notes are color coded.