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- 3D Organic Chemistry Video Course: using molecular modeling software
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Some of our personal favorite tricks:
#9- Fischer projections are a black tie affair
#13- Size Matters: Resonance between equivalent atoms means equal bond lengths
#14- Good for nothing alkanes. Lousy molecules
#16-Beware of the bad acid trip: Meet your strong acids
#17- Meet your strong nucleophiles
#18- They have worn out their welcome--Know your leaving groups.
#19- If you don't start with chirality, you can't end with it
#20- Markovnikov was a Liar
#22- Is it E1, E2, SN1, SN2?
#29- Four Organometallics to Rule Them All
#31- Let's Go Retro: Retrosynthetic Analysis
#34- EAS Strategy: conversion of alkyl groups to carboxylic acids
#35- EAS Strategy: In football, you need good blockers. SO3 and X are our Blocking Groups
#37- EAS Strategy: Substituted toluenes came from toluene. Duh
#46- H2SO4 and HNO3: the good-cop/bad-cop of nitrations
#48 -UFC 1221: Hoffman vs. Zaitsev, the Elimination
#49- Dude, where's my carbocation?
#50- Free Radical Halogenation: The Molecular Handle
#52- Is a Halogen Squatting on Your Molecule? Removing the unwanted halogen
#53- You don't want a D on your transcript, but you might want one on your molecule
#56- It's an urban legend that SN1 reactions give completely racemic products
#57- What do you Amine you're getting rid of me?--How to eliminate an amine
#58- Why Didn't You Say Were Sendin the Wolf? The Wolff-Kishner Reduction
#63- Role Reversal: Nitrile Hydration and the Letts Nitrile Synthesis
#65- Role Reversal: Halogens and Carboxylic Acids
#67- Just Like Kevin Costner to Whitney Houston, Protecting Groups Are Chemical Bodyguards
#83- The Nitrogen Hint (Not a Rule)
#84- Are You a Learner Like Socrates or a Memorizer Like a Super Computer?
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