Instructional Video5:46
SciShow

Is That “New Car Smell” Dangerous?

12th - Higher Ed
Some of us can't get enough of that new car smell. But certain volatile organic compounds (VOCs) that help create this aroma are linked to cancer. While this doesn't mean new car smell definitely increases your chance of getting cancer,...
Instructional Video2:24
SciShow

These Birds Smell Like Tangerines

12th - Higher Ed
On remote, rocky North Pacific islands, you may find a cute little bird that just so happens to smell like tangerines.
Instructional Video10:37
Crash Course

Organometallic Reagents and Carbanions: Crash Course Organic Chemistry

12th - Higher Ed
Have you ever wondered why the gas station has “unleaded fuel” but there isn’t a “leaded” option? The answer has to do with a chemical called tetraethyl lead, which is an organometallic compound, or an organic compound with a...
Instructional Video2:27
SciShow

These Birds Smell Like Tangerines

12th - Higher Ed
On remote, rocky North Pacific islands, you may find a cute little bird that just so happens to smell like tangerines.
Instructional Video2:19
SciShow

Why Do Stink Bugs Stink?

12th - Higher Ed
Turns out stink bugs and cilantro have some things in common.
Instructional Video7:33
Crash Course

Hydrocarbon Derivatives - Crash Course Chemistry

12th - Higher Ed
Functional groups? Functional groups within functional groups? Hank takes today's Crash Course video to discuss some confusing ideas about Hydrocarbon Derivatives, but then makes it all make more sense. -- Table of Contents Alcohols...
Instructional Video11:11
Crash Course

An Overview of Aldehydes and Ketones: Crash Course Organic Chemistry

12th - Higher Ed
Ketones and aldehydes are all around and inside us, from the strong smelling component of nail polish remover, acetone, to hormones in our bodies, to drug treatments for allergies, COVID-19, and even cancer! We’ve already learned a bit...
Instructional Video5:02
Professor Dave Explains

Strecker Amino Acid Synthesis

12th - Higher Ed
Amino acids, nature makes them, and humans have been making them as well since 1850. The first lab synthesis of amino acids was reported by Adolph Strecker, so it's called the Strecker amino acid synthesis, and despite being so ancient...
Instructional Video2:33
Professor Dave Explains

Ozonolysis

12th - Higher Ed
An introduction to ozonolysis.
Instructional Video14:20
Catalyst University

Grignard Reactions: Theory & Practice with Strategy

Higher Ed
Grignard Reactions: Theory & Practice with Strategy
Instructional Video6:31
Professor Dave Explains

Oxidation of Alkenes Using Potassium Permanganate (Hot and Cold Conditions)

12th - Higher Ed
We've seen that KMnO4 can oxidize alcohols and aldehydes to give carboxylic acids and ketones, but this reagent can also oxidize alkenes. The product(s) will be different depending on whether we use cold basic conditions or hot acidic...
Instructional Video3:29
Professor Dave Explains

Reduction of Esters With DIBAL-H

12th - Higher Ed
We know about a lot of different oxidizing and reducing agents that facilitate a variety of different transformations. But we haven't touched upon the precise transformation that can be achieved by diisobutylaluminum hydride, also known...
Instructional Video3:04
Professor Dave Explains

Practice Problem: Reducing Agents

12th - Higher Ed
For this one we need to know the ability of different reducing agents to react with various functional groups.
Instructional Video6:47
Professor Dave Explains

Practice Problem: Crossed Aldol Products

12th - Higher Ed
Enolate chemistry is tricky business! You might get more products than you think. Give this one a shot.
Instructional Video8:40
Professor Dave Explains

Cannizzaro Reaction

12th - Higher Ed
The Cannizzaro reaction is pretty old, over 150 years old in fact, but it is still an important reaction in organic chemistry. It involves the disproportionation of two equivalents of an aldehyde, meaning one is oxidized to the...
Instructional Video3:51
msvgo

Methods of Preparation of Carboxylic Acids

K - 12th
It gives details about the preparation of carboxylic acids.
Instructional Video8:38
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1
Crash Course

Hydrocarbon Derivatives

9th - 12th
This comprehensive video focuses on functional groups including alcohols, hydroxyl groups, aldehydes, carboxylic acid, acetone, ethers, esters, and amines. 
Instructional Video6:10
Socratica

What Are Functional Groups?

9th - Higher Ed Standards
What's the function of functional groups? Explore the portions of biological molecules that make things happen with a video from Socratica's series on biology. The narrator illustrates each major functional group, then describes them in...
Instructional Video7:48
Khan Academy

Aldehyde Introduction, Aldehydes and Ketones, Organic Chemistry

10th - Higher Ed
Sal clarifies a description that he missed in prior videos about the strong smell of amines. He then recaps and compares many of the small and large aldehydes, taking the opportunity to describe their structure and the progression of...
Instructional Video3:54
Curated OER

Lesson 12: More Derivatives, Ketones, Aldehydes, Ethers, Amines

9th - 12th
Lesson 12 in "Chemguy's" series of organic chemistry videos, this one is somewhat of a bonus. He briefly introduces young chemists to the ketones, aldehydes, and amines. He discloses how to name and draw the structures of each.
Instructional Video
Khan Academy

Khan Academy: Nomenclature of Aldehydes and Ketones: Aldehyde Introduction

9th - 10th
Video lecture provides an introduction to Aldehydes. [7:49]
Instructional Video
Khan Academy

Khan Academy: Nomenclature of Aldehydes and Ketones: Ketone Naming

9th - 10th
Explains the differences between aldehydes and ketones, and how to name ketones. [8:44]
Instructional Video
Khan Academy

Khan Academy: Aldehyde Introduction

9th - 10th
A video that introduces the functional group known as Aldehyde. [7:48]
Instructional Video
Khan Academy

Khan Academy: Acid and Base Catalyzed Formation of Hydrates and Hemiacetals

9th - 10th
This video demonstrates how the addition of acid or base can catalyze the formation of hydrates and hemiacetals. [10:26]