Pearson+ Channels

Bronsted Lowry Acids and Bases Acid and Base Classification: Example 1

Acid and Base Titrations: Strong Acid and Base Titration

Understanding Molecular Orbital Theory

Forces in Horizontal Plane

Atoms to Moles to Grams

Projectile Motion: Horizontal Launch

Enthalpy in Thermodynamics

Introduction to Mechanisms: Reactivity Example 1

Oxidation of Sulfides

Understanding Carboxylic Acid Derivative Reactions

Side Chain Halogenation

Exceptions to Ionization Energy in Groups 2A & 3A

Determining the Mean and Standard Deviation of a Discrete Random Variable

Alkene and Alkyne Reactions: Halogenation Example 1

Calculating Molar Mass

Understanding the difference between Atomic Mass & Molecular Mass

Understanding the Expanded Octet

Comparing Acidity with pKas

Functional Groups in Under 5 Minutes - Organic Chemistry

Physical vs Chemical Changes

Molecular Geometry Explained

The s,p, d, f sublevels and the Periodic Table

Welcome to Channels, in Pearson+ | Formerly ClutchPrep

Calculating Radical Yields: Example 1

Vertical Forces & Acceleration

Ideal Gas Law Simplified

Oxidation Reduction (Redox) Reactions Explained

Electronegativity and Dipoles: Types of Bonds Example 2

VSEPR Theory In Under 5 Minutes

Intro to Motion (Kinematics): Acceleration and Motion Equations

Intro to Motion Kinematics: Average Velocity Problems

Electronegativity and Dipoles: Types of Bonds Example 3

How To Draw Lewis Dot Structures

The difference between protic vs. aprotic solvents

Work by Variable Forces & Springs

Freezing Point Depression Explained

Electronegativity and Dipoles: Types of Bonds Example 1

Leaving Group Conversions: Using HX Acids

Thiol and Sulfide Nomenclature

Draw the following declin as a chair conformation in the most stable conformation

Aromatic Hydrocarbons

Alkane Nomenclature: IUPAC Alkane Naming Rule #3

Aromaticity of Annulenes: Example 1

Understanding Heats of Formation

Empirical Formula Calculations Explained in 3 Minutes

Alkene and Alkyne Reactions Hydrohalogenation: Example 1

Strong Oxidative Cleavage

Optical Activity: Specific vs Observed Rotation

Oxidation Mechanisms

Leaving Group Conversions: Using SOCl2 or PBr3

SNAr Mechanism: The Meisenheimer Complex