Aldol condensation - Study guides, Class notes & Summaries

Hydrogenation: H2,Ni high pressure/ H2,Pd - ANSWER-Reducing agent... Reduces Alkynes and Alkenes - Alkanes Aldehydes- primary alcohols Ketones- secondary alcohols Esters- two alcohols Imine- amine Amide- amine Nitrile- primary amine Nitro- amine 10% NaOH - ANSWER-Aldol Condensation 1.O3 2.Zn or Me2S Or 1.03 2.H2O2 - ANSWER-1.Ozonolysis (oxidation of an alkene) 2.Hydrogen peroxide does further oxidation. Product = carboxylic acid Carboxylic acid + 1. Alcohol 2. H3O+ (Work-up...

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.

covering all notes from exam 3 to exam 4. Clasen condensation, crossed claisen, Dieckman condensation, a-halogenation, aldol, LDA, NAH, acetoacetic ester, decarboxylation, malonic ester, conjugate addition, Michael reactions, azide/Gabriel synthesis, reductive animation, amines, Robinson annulation.

THIS DOCUMENT EXPLAIN THE REACTION MECHANISM AND THE CONDITIONS UNDER WHICH ALDEHYDES AND KETONES UNDERGO ALDOL , CROSS ALDOL CONDENSATION , CANIZZARO AND CROSS CANIZZARO REACTIONS

his chapter introduces students to the organic compounds known as aldehydes and ketones, which are characterized by the carbonyl functional group (C=O). Here's an overview of what is usually covered in this chapter: Introduction to Aldehydes and Ketones: Aldehydes and ketones are organic compounds with a carbonyl group, which consists of a carbon atom doubly bonded to an oxygen atom. In aldehydes, the carbonyl group is at the end of the carbon chain, while in ketones, it is found within ...

Beta dicarbonyl and Aldol condensation, Beta carbonyl electrophiles class notes

This chapter contains all necessary information needed to know about the alpha carbon chemistry of carbonyl compounds. These notes are color coded. It contains information about acidity, enolization, alpha halogenation, aldol and claisen condensation reactions, malonic and acetoacetic ester synthesis, conjugate addition and michael addition reactions. Reactions and mechanisms are shown clearly with arrows, and explanations as necessary.

This document is a summary of the alpha carbon chemistry chapter of the organic chemistry 2 course. It is digitally taken handwritten notes. This chapter contains all necessary information needed to know about the alpha carbon chemistry of carbonyl compounds. These notes are color coded. It contains information about acidity, enolizations, alpha halogenations, aldol and claisen condensation reactions, malonic and acetoacetic ester synthesis, conjugate addition and michael addition reactions. Rea...

Enol Enolates and Enamines: Enol Enolates: These are formed by deprotonating an alpha carbon adjacent to a carbonyl group in a molecule containing both a carbonyl and an enolizable proton. They are important intermediates in many organic reactions, particularly in aldol condensation and Claisen condensation reactions. Enamines: These are formed by the reaction of a secondary amine with a carbonyl compound, resulting in the formation of a carbon-nitrogen double bond. Enamines are versatile ...