https://Leah4sci.com/Metallic Presents: Overview of Organometallic Reagents, Formation and Reactions, Including Grignard, Organolithium and Gilman Reagents

Watch next: Grignard reagent, reaction, mechanism and shortcut https://youtu.be/QDju_-r4y3Y

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In this video, you'll learn about the 3 most common organometallic reactions, including how to create the individual reactants, the similarities and differences, and how they react with different types of molecules.
This includes Grignard reagent, organolithium and Gilman or organocuprate.
You will learn how organometallics can be useful in questions of organic synthesis for chain elongation, ring opening reactions and much more.
You will also understand why the carbon in an organometallic reagent is so reactive, acting as a nucleophile in a reaction.

↪ Links and resources mentioned in this video ↩
▸Grignard/Organometallics Series https://Leah4sci.com/Metallic

▸Grignard Reagent Tutorial + Cheat Sheet https://Leah4sci.com/Grignard
▸Polar covalent bond https://youtu.be/PlaFSBt5HTU
▸Nucleophilic analysis and basis for substitution-elimination https://youtu.be/gc_DVjMtD_U
▸Oxidation and Reduction Series + Cheat Sheet https://Leah4sci.com/redox
▸Michael Added https://Leah4sci.com/Enolate

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In this video:
[0:19] Defining organometallic
[1:48] Comparison of reactivity of organometallics
[2:53] Grignard Reagent – Organomagnesium
[5:27] Overview of Grignard's reactions
[6:12] Organolithium reagent
[7:47] Gilman Reagent – Organocuprate

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