Organometallic Reagents and Reactions - Grignard, Gilman, Organolithium
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- Опубликовано: 4 июл 2024
- Leah4sci.com/Metallic presents: Organometallic Reagents, formation and Reactions overview including the Grignard, Organolithium and Gilman Reagents
📺Watch Next: Grignard Reagent, Reaction, Mechanism and Shortcut • Grignard Reagent, Reac...
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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 Leah4sci.com/Metallic
▸Grignard Reagent Tutorial + Cheat Sheet Leah4sci.com/Grignard
▸Polar Covalent Bonding • Ionic, Polar Covalent ...
▸Nucleophile and Base Analysis for Substitution-Elimination • Nucleophile and Base A...
▸Oxidation and Reduction Series + Cheat Sheet Leah4sci.com/redox
▸Michael Addition Leah4sci.com/Enolate
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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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Leah, I really have to thank you for a deeper understanding in organic chemistry!!
You're very welcome! Glad my videos are helping
Thank u mam i was crying that i didnt understand this in coaching
U simplified it a lot
I'm sorry to hear this topic had you in tears, but I'm glad I was able to help clear things up for you!
I love u queeennn, u make this so easy 🤩🤩
Thank you so much! glad to help
Thanks ms Leah ❤
You are so welcome
After a long time you are finally back, we would love to watch your organic chemistry videos regular basis..
Thank you and you are most welcome to. With over 300 videos posted you should hopefully find plenty on any topic you're currently working on
@@Leah4sci keep uploading mam
@@happysinghfrompatiala964 skm sir proud student
@@Leah4scihi mam
Very clear..Thanks
You're very welcome!
Thank youuuu 💐
You're very welcome
Hello mam
I am a student studying in high school in India
I really loved your way of teaching organic chemistry
There is no online tutor in India who can make organic chemistry this easy
Thank you
You're very welcome!
Hey, I love your videos. It has helped me out so much. Thank you.
Can you make an in-depth video on gilmans reagent, it’s a little difficult to understand.
Glad my videos are helping and thanks for the suggestion. I don't know when but I will consider it at some point in the future
I dont have these topics in my syllabus but i understood n i love it more❣️❣️🥰🥰🥰🥰🥰
Awesome that you're understanding it! This usually shows up in organic chemistry part 2
Yeah its great🥰🥰
Hi mam your voice is very nice and your way of teaching is very nice ❤❤❤❤
Thank you for the compliment!
Thank you maam
you're welcome
Tommorow is my exam this video help me alot
I'm so glad to hear that! I hope the exam went well.
After all of the MO theory and structural analysis is done (a tough task in itself), it is always about just two things: 1. where do the electrons want to go? 2. Can they get there? If not, see step one for the next easiest pathway and repeat!.
I like it! So many Organic mechanisms can be simplified by just thinking about the electrons flowing from high density to low density situations. Thanks for watching.
Thanks for the awesome vid :)
May I ask why the Gilman reagent [(CH3)2CuLi] wouldn't just attack the carbonyl carbon?
Also do you have a vid on latent polarity and why it occurs?
You are very welcome!
Regarding why the carbonyl doesn't get attacked, this is considered a weaker attacker and follows a 1,4 addition mechanism. (Review Michael addition for this.)
As for latent polarity, I'm sorry but I don't have a video on this.
@@Leah4sci Ah brilliant, thanks for the reply :)
Awesome
thank you!
Can you tell us how to make a video like this? Can you share what devices you use
Let's keep the comments relevant to the video topic please.
thanks,by the way can u tell me the product of this reaction?:C3H5RCOOH+H2O->?
I'm sorry, but I don't offer tutoring over social media. For help with questions like this and more, I recommend joining the organic chemistry study hall. Details: leah4sci.com/join or contact me through my website leah4sci.com/contact/
What are your best organic chemistry books reference ❤
I prefer my own resources over any textbook! Find my entire free Orgo collection on my website at Leah4sci.com/syllabus.
Or, for details on my membership site and resources, visit Leah4sci.com/join or contact me at Leah4sci.com/contact
I am really struggling in physical chemistry can you pls help me
I'm sorry, but I don't offer tutoring over social media. Additionally, I am not a Physical Chemistry tutor. I help students with Organic Chemistry through my Organic Chemistry Study Hall.
Details for that found at leah4sci.com/join or contact me through my website leah4sci.com/contact/
Reaction with acid chloride shoul be addition and elimination... Therefore first acetone will form..
Are you implying there's a mistake in the video? If yes, thank you for bringing it to my attention. which reaction? (what time in the video?)
@@Leah4sci reaction with acid halide ang grignard reagent... It should be addition via elimination... I mean grignard will react untill u use water... In first step u did not use water.. So first acetone will form... Then again grirnard nucleoplhilic addition occur..
@@Leah4sci in the thumble given...
@@Leah4sci otherwise u r wright... The answer will be decided by the given question....
@@techofbengal3137 I still don't see an error in the video. Water was not added until after the second addition of the Grignard reagent to form the alcohol. An acid halide reacts with excess Grignard reagent to form a tertiary alcohol, NOT a ketone.
Hi mam which software is using to create this animation video
Let's keep the comments relevant to the video topic please. Thanks!
@@Leah4sci not only you are creating the chemistry video in you tube. You thought all science and everything is in your mind, actually you got from alone.
Anyway I got your software by the helps of artificial intelligence, I just paste your video link and asked to artificial intelligence, like below.
Hi their, can you just tell me which software is used to create this video, here I am pasting the youtube video link.
Lol Suddenly with in fractions of second the AI gave me the answer.
😂