Williamson Ether Synthesis Reaction Mechanism

[@TheOrganicChemistryTutor]

Organic Chemistry - Video Lessons: www.video-tutor.net/organic-chemistry.html

[@omarmikha1677]

6:55 "so what's gonna happen here? ..I'LL tell you" lmaooooooooooo idk why that made me crack up

[@pegs9951]

Saaaame

[@petevenuti7355]

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).

[@senny-]

Yeah, i like how it feels like he's letting us in to a favorite little secret that he knows.

[@alinamoreno9235]

thank you for teaching what my professor is supposed to be teaching... self-teaching organic thru online classes is hard :/

[@prajjwalsharma1441]

True 🥲

[@avbalimane]

You mi

[@yessir1400]

did you make it?

[@Jojo-kl6tx]

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.☺

[@forouqam]

Thankyou thank you it is perfect , I hope anywhere you are , be happy as much as you make us happy 😊🌸THANK YOU AGAIN 💙

[@jessicazwilling7456]

Ahhhhmazing how you simplify everything. Orgo is not so scary after all.

[@SonuKumar-me7sw]

I'm an IIT JEE aspirant and your video is best for it 😀❤️

[@ageunggiffarigozali3390]

@ 1:59 It should be "most alcohols are MORE basic than phenol" right ? Since greater pKa means weak acid and thus a better base ?

[@petevenuti7355]

Good catch! I felt something didn't sound right there, I had to look it up though...

[@mackfieldgeorge]

I don't know what I would do without you 🤧😂

[@ffobliv]

fail probably

[@rajaroychoudhuri7451]

Favoulus explanation deserves to be best organic chemistry tutor

[@rebeccaly]

Thank you!! You make it so much easier to understand!

[@BeanJuan]

At 16:16 is that a major product of the reaction along side the cyclo molecule at the end?

[@maximocaceres4685]

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

[@ilovecows303]

does the butyl propyl ether not have an extra carbon since the last two electrons should leave with the bromine?

[@maheradan8050]

Wow thank you, we're going through that now.

[@allyqi8062]

for the part at 7:54, why does it happen again? Thank you!

[@mohamedstes5800]

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?

[@senny-]

thanks as always, man

[@jujua9431]

13:10 how can I know if the alkene will be cis or trans?

[@ebrahimrampuri3690]

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.

[@jesusmrosario-claudio4104]

Thank you once again.

[@saki7952]

Thank you sir. Would you mind uploading frequency distribution table problems Mathematics.

[@rawanayyash3547]

thank youuuuuuu!!!!

[@kacyk7824]

@15:09 What did Sodium say to Bromine at the club when he tried to hit on her ? NaBr = (Nah Bro)

[@yvainestelmack7196]

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

[@abasabdul_salamaliqulijan1433]

thank you for teaching

[@hanupawandwivedi6613]

Nice explanation

[@mahmoudtony6905]

Thank you sir you're awsome ......would you upload the marvelous carbohydrates video please?

[@maxcozzini1604]

During the intramolecular reaction, why was the bromide atom kicked off carbon 6?

[@rekhasharma7412]

Please make a separate video on Williamson continuous ether synthesis Pls pls pls

[@michaeldepauw7446]

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!

[@islamicbrotherhood9574]

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

[@23-01methsara]

Can you say me.what is this notepad software ? Please ❤

[@abduelrahmanelmaghraby2926]

Hey prof. I wanna play vid of alcohol & ether and epoxide reaction but they can't be played ... So what should I do..,?!

[@annikaphase9307]

bless you

[@lukeke235]

would this be possible to produce diphenyl ethers

[@lukekeegan2374]

Is this applicable for diphenyl ethers any help appreciated

[@nejimahmed2201]

Thanks a lot...

[@clementchileshe]

write reaction mechanism for benzyl-tert-butyl ether

[@katurisuryanarayana9927]

Example of Williamson synthesis

[@user-vh4jn4vv8e]

Please make videos on classical and quantum mechanics. A request to you sir.

[@JoudyWahbi-d4q]

I love you

[@LegecyClash]

2025 attendence 😂❤❤

[@khalifaalkhalifa1709]

وحش

[@keqiangpan5661]

i do rate you for boosintg me

[@alexchang24]