2025-10-13
[public] 16.0 views, 3.00 likes, dislikes audio only
Let's break down the SN1 reaction mechanism step-by-step, showing exactly how the leaving group departs, how the nucleophile attacks the alpha carbon, and why the whole process leads to a mixture of enantiomers. Using clear diagrams and curved arrows, we'll walk through how to predict products, avoid common mistakes, and decide when SN1 CAN'T happen.
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0:00 Unimolecular Nucleophilic Substitution Reactions
0:31 SN1 Generic Pattern
3:28 Achiral Easier Example of SN1
7:25 Chiral Complex Example of SN1
8:46 Stereochemistry & Molecular Orbital Theory Explanation
12:55 Ratios of Enantiomeric Products
14:05 SN1 & SN2 Differences: Order of Carbon
15:27 Unimolecular vs Bimolecular: Reactants & Rate Law
16:30 Stereochemistry of SN1 vs SN2
17:20 When SN1 Can't Happen: Methyl & Primary
17:53 Better Leaving Groups & Best Nucleophiles
Citations:
Paula Yurkanis Bruice, "Organic Chemistry" 8th ed
https://openstax.org/books/organic-chemistry/pages/11-4-the-sn1-reaction
Music: https://youtu.be/lL6AsbG07xY