See my comment.... I could see a spoof made from this video by strategic clipping of his words to make some really badass dialog! You might say his tone doesn't fit, wouldn't work, but I think the relaxed tone would just give the impression of being both cavalier and amused by a stressful situation(if that's the kind of dialog you edit together).
Dude, you are AWESOME. Thank you so much. We wrote it down kinda weird in the lecture, so I really couldn't figure the steps out by myself. Your videos are always a great help.☺
so, basically: SN2 reaction your substrate is R'X- and your nucleophile is ROH strong nucleophile required primary carbon, or else you'll also get an E2 if the nucleophile is also a base
At about 2:20 you say hydroxide is strong eneough to deprotonate a phenol but not to deprotonate 1-butanol. Dont you mean water or H2O? Or am i mistaken?
But i think rate of ether synthesis should not be affected by structure of alkoxide...as it has to attack the position and bulkiness of halide will determine the major product
Two boys were fighting in class about whose girlfriend was best. Boy 1: Your girlfriend stinks! Boy 2: Well unlike yours mine's not an atom with 67 protons! Chemical symbol for Holmium: Ho
It depends with E2 reactions. For E2 reactions, Beta hydrogen, and leaving group have to be anti-periplanar which can give us cis alkene. However, usually, the more stable alkene formed is E alkene where largest groups are trans to each other.
At 14:45, you have an error. The H- ion is generally considered a very poor nucleophile and will not act in the way you describe. I love your videos and find them very useful for sharing with my students, but I thought you'd want to maybe correct that little mistake. Thanks!
Organic Chemistry - Video Lessons: www.video-tutor.net/organic-chemistry.html
6:55 "so what's gonna happen here? ..I'LL tell you" lmaooooooooooo idk why that made me crack up
Saaaame
See my comment.... I could see a spoof made from this video by strategic clipping of his words to make some really badass dialog! You might say his tone doesn't fit, wouldn't work, but I think the relaxed tone would just give the impression of being both cavalier and amused by a stressful situation(if that's the kind of dialog you edit together).
Yeah, i like how it feels like he's letting us in to a favorite little secret that he knows.
thank you for teaching what my professor is supposed to be teaching... self-teaching organic thru online classes is hard :/
True 🥲
You mi
did you make it?
Dude, you are AWESOME. Thank you so much. We wrote it down kinda weird in the lecture, so I really couldn't figure the steps out by myself. Your videos are always a great help.☺
Thankyou thank you it is perfect , I hope anywhere you are , be happy as much as you make us happy 😊🌸THANK YOU AGAIN 💙
Ahhhhmazing how you simplify everything. Orgo is not so scary after all.
I'm an IIT JEE aspirant and your video is best for it 😀❤️
so, basically:
SN2 reaction
your substrate is R'X- and your nucleophile is ROH
strong nucleophile required
primary carbon, or else you'll also get an E2 if the nucleophile is also a base
Favoulus explanation deserves to be best organic chemistry tutor
@ 1:59 It should be "most alcohols are MORE basic than phenol" right ? Since greater pKa means weak acid and thus a better base ?
Good catch! I felt something didn't sound right there, I had to look it up though...
I don't know what I would do without you 🤧😂
fail probably
does the butyl propyl ether not have an extra carbon since the last two electrons should leave with the bromine?
Thank you!! You make it so much easier to understand!
Wow thank you, we're going through that now.
At 16:16 is that a major product of the reaction along side the cyclo molecule at the end?
At about 2:20 you say hydroxide is strong eneough to deprotonate a phenol but not to deprotonate 1-butanol. Dont you mean water or H2O? Or am i mistaken?
for the part at 7:54, why does it happen again? Thank you!
During the intramolecular reaction, why was the bromide atom kicked off carbon 6?
But i think rate of ether synthesis should not be affected by structure of alkoxide...as it has to attack the position and bulkiness of halide will determine the major product
@15:09 What did Sodium say to Bromine at the club when he tried to hit on her ? NaBr = (Nah Bro)
Two boys were fighting in class about whose girlfriend was best.
Boy 1: Your girlfriend stinks!
Boy 2: Well unlike yours mine's not an atom with 67 protons!
Chemical symbol for Holmium: Ho
Thank you sir. Would you mind uploading frequency distribution table problems Mathematics.
thanks as always, man
Thank you once again.
13:10 how can I know if the alkene will be cis or trans?
It depends with E2 reactions. For E2 reactions, Beta hydrogen, and leaving group have to be anti-periplanar which can give us cis alkene. However, usually, the more stable alkene formed is E alkene where largest groups are trans to each other.
At 14:45, you have an error. The H- ion is generally considered a very poor nucleophile and will not act in the way you describe. I love your videos and find them very useful for sharing with my students, but I thought you'd want to maybe correct that little mistake. Thanks!
thank you for teaching
Please make a separate video on Williamson continuous ether synthesis
Pls pls pls
Thank you sir you're awsome ......would you upload the marvelous carbohydrates video please?
Nice explanation
Hey prof. I wanna play vid of alcohol & ether and epoxide reaction but they can't be played ... So what should I do..,?!
thank youuuuuuu!!!!
Can you say me.what is this notepad software ? Please ❤
would this be possible to produce diphenyl ethers
Is this applicable for diphenyl ethers any help appreciated
write reaction mechanism for benzyl-tert-butyl ether
Example of Williamson synthesis
Thanks a lot...
Please make videos on classical and quantum mechanics. A request to you sir.
bless you
2025 attendence 😂❤❤
I love you
i do rate you for boosintg me
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