Specific Rotation calculations are a useful tool in optical activity. This video will help you understand the factors influencing specific rotation such as observed rotation, g/mL, path-length, wavelength, and temperature. You will see a detailed breakdown of the equation along with a few examples to follow along. (Watch on YouTube: Optics 2. Click CC for video transcription.) <– […]
Enantiomeric excess percentage (aka optical purity percentage) calculations are one of the few equations you’ll come across in your orgo course. This video gives you a step by step breakdown and practice examples. You’ll see how to find the percent excess via logic and see the numbers side by side. (Watch on YouTube: Optics 3. Click […]
Polarimetry is the key to understanding chiral molecules in terms of optical activity. This video goes behind the scenes of the polarimeter to help you understand what plane polarized light has to do with chiral molecules. Part 1 (of 3) in this mini series explains + D and – L, dextrorotatory and levorotatory, and their (lack […]
Chirality/Stereochemistry Video Series: Video 4 R and S configurations are pretty straight-forward when priority group #4 is conveniently in the back of the molecule. There’s even a quick trick for when group #4 is forward (as taught in this video). But what happens when priority group #4 is in the plain of the page? Do […]
Chirality/Stereochemistry Video Series: Video 3 This video shows you why and how to reverse R and S when group #4 is forward to help you quickly and easily master relative configurations when studying chirality and stereochemistry. (Watch on YouTube: Group 4. Click cc on bottom right for video transcription.) <– Watch Previous Video: R and […]
Chirality/Stereochemistry Video Series: Video 6 Fischer projections provide a simple 2-dimensional representation for complex 3-dimensional structures. Which is great for drawing complex molecules, but not so much fun if asked to determine R and S configurations. Many books and professors will have you redraw the Fischer projection into a 3-dimensional sawhorse or skeletal structure. I […]
Chirality/Stereochemistry Video Series: Video 5 R and S configurations are found by ranking substituents on a chiral carbon. This is relatively straight-forward when substituents contain 1-3 atoms. This gets more confusing when the substituents are long, complex, and contain many of the same atoms. This orgo tutorial video shows you how to approach lengthy and […]
Chirality/Stereochemistry Video Series: Video 7 Finding R and S configurations for non-traditional molecules can be somewhat tricky. This video teaches you how to quickly find configurations of molecules presented in a Newman Projection. Learn how to view the molecule and quickly assign priority WITHOUT the need to redraw into a sawhorse projection. (Watch on YouTube: […]
Chirality/Stereochemistry Video Series: Video 2 Chiral carbons are identified as having 4 unique substituents. Finding the Absolute Configuration – R and S comes as a result of ranking and order substituents, specifically by noting the configuration of the top 3 groups. This video shows you how to prioritize substituents to find R and S configurations […]
Chirality/Stereochemistry Video Series: Video 1 Chirality is an exciting but potentially tricky topic in organic chemistry. Why? because it’s tough to visualize 2-dimensional drawings as a 3-dimensional structure. But don’t be like the thousands of students struggling with this topic. My chirality series will take you through this topic step by step to ensure that […]
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