[ Ссылка ] presents: Organometallic Reagents, formation and Reactions overview including the Grignard, Organolithium and Gilman Reagents
📺Watch Next: Grignard Reagent, Reaction, Mechanism and Shortcut [ Ссылка ]
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In this video, you’ll learn about the 3 most common organometallic reactions including how to create the individual reagents, similarities and differences, and how they react with different molecule types
This includes the Grignard reagent, organolithium, and Gilman or organocuprate.
You’ll learn how organometallics can be useful in organic synthesis questions for chain elongation, ring-opening reactions and more.
You’ll also understand why the carbon in an organometallic reagent is so reactive, acting as the nucleophile in a reaction.
↪ Links & Resources Mentioned In This Video ↩
▸Grignard/Organometallics Series [ Ссылка ]
▸Grignard Reagent Tutorial + Cheat Sheet [ Ссылка ]
▸Polar Covalent Bonding [ Ссылка ]
▸Nucleophile and Base Analysis for Substitution-Elimination [ Ссылка ]
▸Oxidation and Reduction Series + Cheat Sheet [ Ссылка ]
▸Michael Addition [ Ссылка ]
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⏱ In this video:
[0:19] Defining Organometallic
[1:48] Comparing Reactivity of Organometallics
[2:53] Grignard Reagent - Organomagnesium
[5:27] Grignard Reactions Overview
[6:12] Organolithium Reagent
[7:47] Gilman Reagent - Organocuprate
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