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Crash Course
Crossed Aldol Reactions, Enones, and Conjugate Addition: Crash Course Organic Chemistry
Insects can communicate with each other about all kinds of things, but instead of using words, they use… you guessed it! Organic Chemistry! Insects can send signals to each other by secreting compounds, and one such compound used by...
Crash Course
The Aldol and Claisen Reactions: Crash Course Organic Chemistry
Organic chemistry is a great workout for your brain, and to keep its energy up, your brain needs glucose. To maintain blood glucose levels, our bodies go through a process called gluconeogenesis, which involves the important type of...
Crash Course
E1 and E2 Reactions - Crash Course Organic Chemistry
We’ve spent the last few episodes talking about substitution reactions, but now it’s time to talk about a related type of reaction: elimination reactions! Elimination reactions are super important because they are the main way we can...
Crash Course
Enols and Enolates - Reactivity, Halogenation, and Alkylation: Crash Course Organic Chemistry
You may know that cows produce methane, which is a big concern when it comes to global heating, but did you know that organic chemistry provides a potential solution to this problem? Feeding cows small amounts of red seaweed can greatly...
Bozeman Science
Neutralization Reaction
In a neutralization reaction (or acid-base reaction) a proton is transferred from the Brinsted--Lowry acid to the Brinsted--Lowry base. Water is amphoteric and so it can serve as either an acid or a base in a neutralization reaction. ...
Crash Course
Carboxylic Acid Derivatives & Hydrolysis Reactions: Crash Course Organic Chemistry
Esters have a wide range of uses, from giving perfumes and colognes their fragrances, to preventing diseases like scurvy. Vitamin C, that scurvy preventing antioxidant, is derived from carboxylic acids, a class of organic compounds we’ve...
Bozeman Science
Acid-Base Equilibrium
In this video Paul Andersen explains how acid-base chemistry can be understood in terms of equilibrium. Water is present in all acid-base chemistry and is amphoteric in nature. The Ka and Kb values can be used to determine the strength...
Professor Dave Explains
Enantioselective Hydrogenation of Carbonyls and Imines
We just learned about some innovations regarding enantioselective hydrogenation of alkenes which utilize homogeneous catalysis and chiral catalysts. Can we employ the same approach to hydrogenate other functional groups? What about...
Professor Dave Explains
The Haloform Reaction
Once again, we will be interested in learning about reactions that break carbon-carbon bonds, as this will allow us to perform necessary transformations on substrates. The haloform reaction is one such reaction, and it is commonly used...
Professor Dave Explains
Aldol Condensation
Introducing aldol condensation and enolate chemistry in general.
Professor Dave Explains
Wolff-Kishner Reduction
How can we reduce a ketone or aldehyde all the way to the alkane? We already learn one way, Clemmensen reduction. But what if we don't have any amalgamated zinc handy, you ask? Well there's an older way called Wolff-Kishner reduction....
Catalyst University
Buffers: ICE Problem With Henderson-Hasselbalch Equation
Buffers: ICE Problem With Henderson-Hasselbalch Equation
Professor Dave Explains
Practice Problem: Conversion of trans-2-butene to cis-2-butene
How can we go from one type of alkene to another? In three steps precisely? Use the reactions you know and figure it out! (Hint: Think about addition reactions, elimination reactions, and hydrogenations!)
Professor Dave Explains
IIT/JEE Chemistry Practice #31: Acids and Bases
Practice REAL problems from actual past IIT/JEE exams with Professor Dave!
Professor Dave Explains
Practice Problem: Crossed Aldol Products
Enolate chemistry is tricky business! You might get more products than you think. Give this one a shot.
Professor Dave Explains
Practice-Problem: Two-Reaction Pathway
This time we have a starting material, and we are gonna do just two reactions. But it's a little tricky! See if you can figure it out.
Professor Dave Explains
Practice Problem: Drawing Substitution and Elimination Products (SN1/SN2/E1/E2)
I know you guys are dying for more practice choosing between SN1/SN2/E1/E2 mechanisms, so hopefully this one helps a little. Make sure to look at all the factors we talked about in my tutorial on this topic!
Professor Dave Explains
Choosing Between SN1/SN2/E1/E2 Mechanisms
When looking at a substrate and a base/nucleophile, how do we know which one of the basic mechanisms will occur? Let's get some tips in here!
Catalyst University
Titration Curves: A Conceptual Math-based Approach
Titration Curves: A Conceptual Math-based Approach
Professor Dave Explains
Claisen Condensation and Dieckmann Condensation
Introducing Claisen condensation and Dieckmann condensation.
Professor Dave Explains
Alkyne Synthesis by Double Dehydrohalogenation
An overview of alkyne synthesis via double dehydrohalogenation.
msvgo
Ionization of Acids and Bases
It explains the ionisation of acids and bases. It explains the term conjugate acids and bases. It derives the expression to calculate ionic product of water.
Professor Dave Explains
Neutralization Reactions
We know about acids and bases, and we know about acid-base reactions, so what is a neutralization reaction?