Wittig reaction Study guides, Class notes & Summaries

All notes are taken from the textbook and summarized for easy learning. Pictures, diagrams, and synthesis reactions are made in great detail. These are the notes I used to get a 98 in the class.

This document is a summary of the aldehydes and ketones chapter of the organic chemistry 2 course. It is digitally taken, handwritten notes. 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 and shortened for easy understanding and reviewing.

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.

These lecture notes cover a wide range of topics, from the basics of molecular structure and bonding to the intricate mechanisms of organic reactions. Whether you're a beginner seeking a solid foundation or an advanced learner looking to deepen your knowledge, this resource caters to all levels of expertise

(3E)-4phenyl-3-buten-2-one was synthesized using Green utilising a Wittig reaction between Benzaldehyde and Methyl (triohenylphosphoranylidene) acetate. A product of (3E)-4phenyl3-buten-2-one was obtained and its mass was calculated to be 0.36g and the %yield was calculated to be 29%. The retention factors were calculated to be 0.35 and 0.19 for Benzaldehyde and the product respectively.

CFQ & PP: Carbonyl Chemistry: Survey of Reactions and Mechanisms Reading Brown and Foote: Sections 15.1, 16.6 – 16.11, 16.13, 16.14 17.4 – 17.8, 18.2 and 18.4 – 18.12 Lecture Supplement Carbonyl Reaction Catalysis (page 50 of this Thinkbook) Suggested Text Exercises Brown and Foote: Chapter 15: 1, 2 Chapter 16: 4 – 11, 12 – 14, 19 – 45, 54 – 68 Chapter 17: 2 – 5, 18 – 43 Chapter 18: 2 – 12, 20 - 53 Optional Interactive Organic Chemistry CD and Workbook Supporting...

Three types of reaction are explained in these notes with mechanism of reaction.

In depth notes including plenty of reactions and diagrams and breakdowns of mechanisms

Protecting groups, reductive amination, Primary and secondary amine reactions with ketone, reverse wittig reaction, design a synthesis, alkyne substitution, base and substitution reaction, KrCrO3 in acid (H2SO4) Jones oxidation, Swern oxidation, enamine and imine. All answered - great worksheet exam prep and organic chemistry knowledge!

Protecting groups, reductive amination, Primary and secondary amine reactions with ketone, reverse wittig reaction, design a synthesis, alkyne substitution, base and substitution reaction, KrCrO3 in acid (H2SO4) Jones oxidation, Swern oxidation, enamine and imine. All answered - great worksheet exam prep and organic chemistry knowledge!