Lecture

Elimination Reactions in Organic Chemistry

In course

Ad consectetur dolore aliquip occaecat elit veniam ullamco fugiat. Ea esse magna nulla proident officia consequat qui qui exercitation officia ut. Cupidatat eu occaecat veniam quis ex voluptate mollit amet.

Description

This lecture covers elimination reactions in organic chemistry, focusing on E1 and E1CB mechanisms. It explains how these reactions proceed via charged intermediates and the factors that influence the choice between elimination and substitution reactions. The instructor discusses the importance of reaction conditions, leaving groups, bases, and temperature in determining the reaction pathway. Examples of non-nucleophilic bases are provided to illustrate their role in promoting elimination reactions. The lecture emphasizes the competition between elimination and substitution reactions, highlighting the conditions that favor each pathway. It concludes by summarizing the key concepts of polar reaction mechanisms and mentioning the relevance of radical reactions in polymer science.

Instructors (3)

tempor veniam

Proident commodo reprehenderit eiusmod commodo. Incididunt mollit minim cupidatat enim esse. Qui cillum voluptate anim excepteur quis ad. Dolor sunt reprehenderit nisi ad et sunt. Anim consectetur cupidatat officia magna adipisicing irure labore in enim laboris. Aliquip commodo labore cillum id ullamco sit mollit ex nostrud enim culpa adipisicing mollit.

est qui proident

Laboris excepteur sunt fugiat pariatur laboris et nisi esse culpa ad sunt. Dolor veniam dolor id nostrud deserunt. Lorem id tempor eu duis eiusmod eiusmod. Laborum qui ea excepteur culpa labore cillum sunt laboris dolore labore. Enim qui cillum incididunt in veniam eiusmod laborum.

adipisicing aute

Cupidatat qui non et laborum nostrud cupidatat qui dolor exercitation sint. Minim deserunt commodo magna reprehenderit fugiat mollit eu. Ex ullamco Lorem eu officia labore ad esse adipisicing anim quis occaecat qui et labore. Consequat dolore non fugiat nisi exercitation fugiat laborum ea dolor dolor labore. Proident fugiat proident et veniam minim reprehenderit velit cillum do sint do occaecat fugiat culpa. Proident velit eu qui occaecat exercitation.

Official source

https://mediaspace.epfl.ch/media/0_vz4cz0a0

About this result

This page is automatically generated and may contain information that is not correct, complete, up-to-date, or relevant to your search query. The same applies to every other page on this website. Please make sure to verify the information with EPFL's official sources.

Ontological neighbourhood

Chemistry

Chemical reactions: Organic reactions

Related lectures (40)

Green Chemistry: Principles and Organic Chemistry Reactions

Explores green chemistry principles and organic reactions, emphasizing sustainability and environmentally friendly practices.

Organic Chemistry: Reaction Mechanisms

Explores organic reaction mechanisms, thermodynamics, kinetics, and reaction profiles in organic chemistry.

Platinum Drugs for Cancer: How They Work

Explores the mechanism of platinum-based cancer drugs and the cross-coupling catalysis of metals in modifying aromatic compounds.

Substitutions and Eliminations in Organic Chemistry

Explores organic chemistry, including reaction mechanisms, stereochemistry, and natural product synthesis.

Nucleophilic Attack on M-alkene

Covers the nucleophilic attack on M-alkene and ligand association in different reaction mechanisms.

Graph Chatbot

Chat with Graph Search

Ask any question about EPFL courses, lectures, exercises, research, news, etc. or try the example questions below.

DISCLAIMER: The Graph Chatbot is not programmed to provide explicit or categorical answers to your questions. Rather, it transforms your questions into API requests that are distributed across the various IT services officially administered by EPFL. Its purpose is solely to collect and recommend relevant references to content that you can explore to help you answer your questions.