Instructional Video11:06
Crash Course

More EAS - Electron Donating and Withdrawing Groups: Crash Course Organic Chemistry

12th - Higher Ed
In the previous episode we discussed what happens when we use electrophilic aromatic substitution to add a group to a benzene ring, but what happens when you try to add even more groups? Well, things get a little more complicated. In...
Instructional Video6:59
Curated Video

Rules for Writing Resonating Structures: Get Them Right!

9th - Higher Ed
When writing resonance structures, it's essential to follow certain rules: only electrons move, not atoms; all structures must have valid bonding; and charges should be minimized. These guidelines ensure resonance structures accurately...
Instructional Video2:12
Curated Video

Conditions for Resonance: Why Acetamide and Carbonate Matter

9th - Higher Ed
Resonance requires specific conditions for electron delocalization. The molecule must have a conjugated system with alternating single and double bonds, and atoms must be capable of sharing electrons. Acetamide and the carbonate ion are...
Instructional Video3:47
Curated Video

Resonance in Action: Bond Length, Acidity & More!

9th - Higher Ed
Resonance has far-reaching effects on molecular properties. It can equalize bond lengths, making double bonds longer and single bonds shorter than expected. It also stabilizes charged species, influencing acidity and basicity. For...
Instructional Video4:59
Curated Video

Pi-n Conjugation: Unlocking the Secrets of Molecular Stability

9th - Higher Ed
Pi-n conjugation occurs when a lone pair of electrons (n) interacts with a pi system, enhancing electron delocalization. This conjugation stabilizes the molecule, as the lone pair contributes to the overall resonance. Pi-n conjugation...
Instructional Video5:59
Professor Dave Explains

Organocuprates (Gilman Reagents)

12th - Higher Ed
We've seen organometallic reagents featuring magnesium, as well as lithium, so how about copper? These are called organocuprates, or sometimes Gilman reagents. What do they look like? How do we make them? What do we do? Let's take a look!
Instructional Video4:30
Professor Dave Explains

Addition on Conjugated Polyunsaturated Systems

12th - Higher Ed
Looking at how addition reactions occur on conjugated polyunsaturated systems.
Instructional Video5:28
Professor Dave Explains

Diazomethane Synthesis and Applications (Arndt-Eistert Homologation)

12th - Higher Ed
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...
Instructional Video4:35
Professor Dave Explains

Aldol Condensation

12th - Higher Ed
Introducing aldol condensation and enolate chemistry in general.
Instructional Video5:22
Professor Dave Explains

Michael Addition

12th - Higher Ed
More enolate chemistry with the Michael addition.
Instructional Video2:46
Professor Dave Explains

Practice Problem: Site of Protonation on a Weak Base

12th - Higher Ed
For this one we will need to understand the basics about Bronsted-Lowry acid-base reactions, and we also should be able to gauge the stability of various potential conjugate bases.
Instructional Video14:26
Professor Dave Explains

Organic Chemistry Practice Exam 12

12th - Higher Ed
Organic Chemistry Practice Exam 12
Instructional Video15:35
Professor Dave Explains

Organic Chemistry Practice Exam 8

12th - Higher Ed
Organic Chemistry Practice Exam 8
Instructional Video12:07
Professor Dave Explains

Resonance Structures/Assigning Formal Charge

12th - Higher Ed
Looking at resonance structures for organic molecules and learning how to determine formal charge.
Instructional Video15:52
Professor Dave Explains

Ortho/Meta/Para Directors

12th - Higher Ed
A discussion of ortho/para directing and meta directing behavior amongst substituted benzenes.
Instructional Video
Khan Academy

Khan Academy: Relative Stability of Amides, Esters, Anhydrides & Acyl Chlorides

11th - 12th
Sal Khan visually explains the relative stability of amides, esters, anhydrides, and acyl chlorides. [11:08]