[ Ссылка ] for video on jOeCHEM and attached worksheet + solution (below video on jOeCHEM aka the link).
Worksheet: [ Ссылка ]
Worksheet Solution: [ Ссылка ]
Worksheet Solution Walkthrough: [ Ссылка ]
Study Guide: (To be created, but Joe's working on it!)
In this video, we discuss why the Free Radical Halogenation reaction comes up short (and doesn't work) in terms of halogenating an allylic carbon. Instead, we talk about how to leverage NBS (N-bromo succinimide) in order to brominate the allylic position, opening up a world of possibilities.
Related videos:
[ Ссылка ] - Free Radical Halogenation - Part 1 - The Mechanism
[ Ссылка ] - Halogenation of a Double Bond with Bromine and Chlorine
========================================
Follow jOeCHEM on social media:
If you're having an organic blast, please SUBSCRIBE: [ Ссылка ]
LIKE and FOLLOW across social media:
Facebook - [ Ссылка ]
Instagram - [ Ссылка ]
TikTok - [ Ссылка ]
Ещё видео!