OChem Cheat Code: 2nd Best Resonance Rule Predicts Nuc/Elec FAST! скачать в хорошем качестве

OChem Cheat Code: 2nd Best Resonance Rule Predicts Nuc/Elec FAST!

Do you wish there was an OChem tip or trick to predict nucleophilic and electrophilic sites?: the 2nd best resonance contributor usually shows where a molecule is actually reactive. In this OChemNinja pro tip, you’ll use the “2nd best rule” to predict where molecules react - even if you’ve never seen the molecule before. We’ll apply it to: 🧑‍🎓 Markovnikov addition to alkenes (why that regioselectivity happens) 🧑‍🎓 Protonated carbonyls (why they’re electrophilic at carbon) 🧑‍🎓 Diels-Alder regioselectivity 🧑‍🎓 Electrophilic aromatic substitution directing effects (ortho/para vs meta) #OrganicChemistry #OChem #Resonance #DielsAlder #EAS Links to Mentioned Videos: Playlist: Full "How Organic Chemistry Reactions Work" Playlist:    • Radical Reactions Overview: Homolytic vs. ...   Markovnikov's Rule:    • Are You Understanding Markovnikov's Rule W...   Ranking Resonance Contributors:    • Rank Resonance Contributors with These 4 R...   Bouncing Arrow Notation:    • Bouncing Arrows Fix Ambiguous Mechanisms i...   90 Sec Mech: Acetal Formation:    • #90SecMech - Acetal Formation   EDG/EWG Modulating Electron Density:    • There are Only: 2 Ways to Modulate Electro...   Contents: 0:00 Intro 00:35 Organic Chemistry Is Predictive 01:19 Markovnikov Addition Explained by Resonance 02:10 Ranking Resonance Contributors 02:58 The 2nd Best Rule Reveals Reactivity 03:57 Protonated Carbonyls Are Electrophilic at Carbon 05:13 Diels-Alder Regioselectivity Without Memorization 07:13 EAS Directing Effects via Resonance