Organic Chemistry - Ch 1: Basic Concepts (10 of 97) Isomers of Pentane (3)
Visit http://ilectureonline.com for more math and science lectures! In this video I will explain the properties (3) or isomers of pentane. Next video in this series can be seen at: https://youtu.be/PLcBkzZ5smY
From playlist ORGANIC CHEMISTRY CH1 INTRODUCTION
Stereoselective Reduction of 4-tert-butylcyclohexanone
CSUN Chemistry and Biochemistry department 1st Semester Organic Chemistry Lab Stereoselective Reduction of 4-tert-butylcyclohexanone Ref: Chem 333 lab manual spring 2020 Made by: Benjamin D. Azmon with special thanks to Kenny Cooper, Fredric Ferrar, Kevin Ng
From playlist 333L OChem 1
Boron Aldol Reaction - Organic Chemistry, Reaction Mechanism
An introduction to diastereoselective aldol reactions using soft enolisation techniques to selectively synthesise one enolate geometry and a Zimmerman-Traxler transition state model to form the new C-C bond and two new stereogenic centres (stereocentres) at the same time. #organicchemistr
From playlist Models in Organic Chemistry
NITRATION TIME! Making A Chemical Called Nitrobromobenzene
In this video we are going to nitrate bromobenzene to make nitrobromobenzene. Patreon: https://www.patreon.com/thyzoid Discord: https://discord.gg/UrjAt44HWH (Let me know if the discord link does not work) Instagram: https://www.instagram.com/thyzoyd/?hl=de š¦ Twitter: https://twitter.com/
From playlist Organic Chemistry
Nitration of MethylBenzoate and Nitration of Bromobenzene
This organic chemistry video tutorial discusses the reaction mechanism of the nitration of methylbenzoate and the nitration of bromobenzene. Subscribe: https://www.youtube.com/channel/UCEWpbFLzoYGPfuWUMFPSaoA?sub_confirmation=1 Access to Premium Videos: https://www.patreon.com/MathScienc
From playlist New Organic Chemistry Playlist
Synthesis of a Bromoalkane (n-Bromopropane)
In this video, I will be making n-bromopropane by brominating 1-propanol. The n-bromopropane can then be used in a Grignard reaction to make butyric acid (smell of vomit). Here is the video of me using it in a Grignard reaction: http://youtu.be/_wmx65zQk58 This process can be used as a
From playlist Syntheses and Demonstrations
Carbon Trifluoromethylation (IOC 49)
In this video, I discuss the radical, nucleophilic, and electrophilic trifluoromethylation in C-CF3 bond forming reactions. https://www.patreon.com/thatchemist Community Discord - https://discord.gg/QWNPETtPcZ I forgot to mention in the video that the Ritter lab developed a TTF-CF3 reag
From playlist Organic Chemistry Lectures
Synthesis Workshop: Chiral N-Heterocyclic Carbene Synthesis with Dr. Vasudevan Dhayalan (Episode 76)
In this Research Spotlight episode, Dr. Vasudevan Dhayalan takes us through his work on the synthesis of chiral N-heterocyclic carbene organocatalysts. This episode has been made possible through a collaboration with Thieme Chemistry (Twitter: @thiemechemistry) and is made in recognition o
From playlist Special Topics: Organocatalysis
Total Synthesis of Ocellatusone C
An organic chemistry minilecture on 'Taming Shapeshifting Anions: Total Synthesis of Ocellatusone C' by Andre Sanchez and Thomas J. Maimone*. It features a highly fluxional bishomoaromatic system that takes part in a Cu-accelerated Stille coupling, borylation and oxidation chemistry, in ad
From playlist Total Synthesis
Synthesis Workshop: Catalytic Hauser-Kraus Annulations with Mohammed Sharique (Episode 21)
In this video, we are joined by Mohammed Sharique (PhD student, Tambar group, UT Southwestern) who takes us through his recently published work on N-heterocyclic carbene catalyzed Hauser-Kraus annulations. --- References --- Main reference: Sharique, M.; Tambar, U. Chem. Sci. 2020, 11,
From playlist Special Topics: Organocatalysis
Carbenes Part 2: Cyclopropanation, C-H Insertion, and the Bamford-Stevens Reaction
In the previous tutorial we learned about carbenes. So now that we understand their properties, we are ready to learn about what we can do with them. Three major uses of carbenes involve cyclopropanation, C-H insertion, and the Bamford-Stevens reaction. Let's see what these are now! Watch
From playlist Organic Chemistry
Making a Polyene with Metals - Retrosynthesis
Organic Chemistry: Retrosynthesis of this polyene hydrocarbon exploiting symmetry and transition metal catalysis for the stereoselective formation of C-C bonds. This fully conjugated polyene has rotational symmetry about its centre. A powerful disconnection for dienes and more extended co
From playlist Retrosynthesis
Diazomethane Synthesis and Applications (Arndt-Eistert Homologation)
In learning about carbenes, we discovered the importance of diazomethane. So it will be a good idea to learn how to make this molecule, as well as some other things we can do with it, including something called the Arndt-Eistert reaction. Check it out! Watch the whole Organic Chemistry pl
From playlist Organic Chemistry
Chemistry - Nomenclature Fundamentals: Anions with 2 Elements (15 of 23)
Visit http://ilectureonline.com for more math and science lectures! In this video I will explain the nomenclature of anions with 2 elements.
From playlist Michel van Biezen: CHEM - Introduction
2021 Heterocyclic Chemistry - Lecture 1
Lecture 1 - General Reactivity Part 1
From playlist Heterocyclic Chemistry 2021
Diazonium Substitution - Sandmeyer Reactions (IOC 38)
In this episode, I go through the various substitution of diazonium salts to nitriles, thiols, halides, sulfonyl chlorides, hydrogen, phenols, and boranes. Variants of this reaction include the Balz-Schiemann reaction, as well as the Rosenmund-von Braun reaction. -----------------------
From playlist Organic Chemistry Lectures
Thanks to Bespoke Post for sponsoring this video! New subscribers get 20% off their first box of awesome ā go to https://bespokepost.com/thatchemist20 and enter code THATCHEMIST20 at checkout. This is the Vitamin Tierlist - vitamins play many important roles in our bodies and the biochemi
From playlist Chemistry Tierlists
Aspirin to Acetaminophen - Part 6 of 6: Acetaminophen from p-aminophenol
This is the final part of the series, where the p-aminophenol is converted to the acetaminophen. Using acetic anhydride, the p-aminophenol is going to be acetylated. The reaction is carried out in water at room temperature. Acetic anhydride does react with water, but it happens slowly.
From playlist Aspirin to Acetaminophen (Parts 1 to 6)
2021 Heterocyclic Chemistry - Lecture 2
Lecture 2 - General Reactivity Part 2
From playlist Heterocyclic Chemistry 2021
