Introduction to Organometallic Compounds
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- Опубликовано: 3 окт 2024
- This organic chemistry video tutorial provides a basic introduction into organometallic compounds. It discusses grignard reagents, organolithium reagents, DIBAH, LiALH4, LiAl(OR)3H, and gilman reagents. It explains how to use the gilman reagents to displace halides to form carbon-carbon bonds. It also explains how to convert acid chlorides and esters to alcohols, aldehydes and ketones.
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I’m so overwhelmed with all these orgo 2 videos! They are great! I just finished it this semester and although I didn’t have these to help me through the class I feel it is so well taught and can help future students.
I love u so much I swear
@@omarmaher1 why do you?
I was literally just reading about electronic waste and how researchers are using organic electronics to reduce waste. Perfect timing! Keep up the great work.
This doesn't have anything to do with that
your explanations are so awesome. I am really grateful about finding your channel. Thank you!
thank you sir i am writing this to you during my final exam. thanks for helping me through school
i gues this was a serious exam bro
Could you please do more Organometallic Videos? Love your explanations! ❤️
Could you do more organometallic videos like suzuki, alkene metathesis, etc
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It really helps me for strong basics (thank you )
that's a work of a genius, thanks for the teaching.
i need your help man
For the first time, a video of yours is confusing me 😩
You can make a grignard in e.g. benzene and toluene, especially if you start from bromo benzene, and other aromatic halogenids
Sir make other organomettalic compounds videos
Great explanation sir
Why oxyrane and oxetane ethers cannot be used in case of organometallic compound
Why not start from definition,classification and nomenclature 😔 because this is confusing
Thats on you to go back and watch those, not him to go from ~Lecture 10 back to Lecture 1.
My guy, that's O-chem 1 lol.
You should definitely know that if you’re watching this video bud
Brother your explanation was so good
But more electronegativity difference means more ionic character which means stronger electrostatic attraction which means it is less easy to break which means it will be less reactive. 9:07
I am in doubt here. Can anyone clear my doubt. Thanks!
Because polar reagents react react with polar compounds here alkyl halide and all these reagents are polar so like dissolve like
Thank you once again.
Which mechanism does it follows
Did you mean to say Mg at 1:10? You put the partial positive charge above it and not Br
I was looking for this comment
Kindly share with me the recommended books for Organic chemistry II, I want reaction mechanisms
Plz what's the ordre of reactivity between n - butyl lithium and s - butyl lithium !!!
13:41 how did you form the ether if there was no other place to grab a and attack a methyl?
nvm its a negative charge that attacks the proton on acid and you said it in the audio. my b
This is orgo 2?? I'm learning this in orgo 1 rb
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@@donnaa7640 bro didnt you hear him hes learning this in ochem 1
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Is it “grin-it” or “gring yard” reaction? Phonetically…
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What's the name of this reagent" c-cd "?
Anybody knows ?
16:39
My DIDDLE UPLOADED
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