Williamson Ether Synthesis Reaction Mechanism

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This organic chemistry video tutorial provides a basic introduction into the williamson ether synthesis reaction mechanism. It contains plenty of examples and practice problems.
Alcohol Reactions - HBr, PBr3, & SOCl2: • Alcohol Reactions - HB...
Free Radical Reactions:
• Free Radical Reactions
Reactions Summary:
• Organic Chemistry Reac...
Organic Chemistry 1 Final Exam Review:
• Organic Chemistry 1 Fi...
IR Spectroscopy:
• IR Spectroscopy - Basi...
Mass Spectrometry:
• Mass Spectrometry
______________________________
Proton NMR Spectroscopy:
• Proton NMR Spectroscop...
Carbon-13 NMR Spectroscopy:
• Carbon-13 NMR Spectros...
Ethers and Epoxides:
• Ether and Epoxide Reac...
Diels Alder Reaction:
• Diels Alder Reaction
Organic Chemistry 2 Final Exam Review:
• Organic Chemistry 2 Fi...

Опубликовано:

30 апр 2018

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Комментарии : 51

@TheOrganicChemistryTutor 6 месяцев назад

Final Exams and Video Playlists: www.video-tutor.net/

@omarmikha1677 4 года назад

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

@pegs9951 4 года назад

Saaaame

@petevenuti7355 2 года назад

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- Месяц назад

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

@alinamoreno9235 3 года назад

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

@prajjwalsharma1441 3 года назад

True 🥲

@avbalimane 3 года назад

You mi

@yessir1400 5 месяцев назад

did you make it?

@Jojo-kl6tx 5 лет назад

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 3 года назад

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

@rebeccaly 4 года назад

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

@jessicazwilling7456 5 лет назад

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

@rajaroychoudhuri7451 4 года назад

Favoulus explanation deserves to be best organic chemistry tutor

@maheradan8050 6 лет назад

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

@SonuKumar-me7sw Год назад

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

@saki7952 6 лет назад

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

@radicalpisces 6 месяцев назад

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

@jesusmrosario-claudio4104 3 года назад

Thank you once again.

@hanupawandwivedi6613 6 лет назад

Nice explanation

@mahmoudtony6905 6 лет назад

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

@abasabdul_salamaliqulijan1433 3 года назад

thank you for teaching

@senny- Месяц назад

thanks as always, man

@allyqi8062 6 лет назад

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

@rawanayyash3547 Год назад

thank youuuuuuu!!!!

@nejimahmed2201 6 лет назад

Thanks a lot...

@lukekeegan2374 4 года назад

Is this applicable for diphenyl ethers any help appreciated

@lukeke235 4 года назад

would this be possible to produce diphenyl ethers

@abduelrahmanelmaghraby2926 2 года назад

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

@islamicbrotherhood9574 3 года назад

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

@mackfieldgeorge 8 месяцев назад

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

@literally_ganyu 2 месяца назад

fail probably

@maxcozzini1604 Год назад

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

@BeanJuan Год назад

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

@ageunggiffarigozali3390 4 года назад

@ 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 2 года назад

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

@rekhasharma7412 10 дней назад

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

@mohamedstes5800 8 месяцев назад

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?

@user-vh4jn4vv8e 5 лет назад

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

@jujua9431 4 года назад

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

@ebrahimrampuri3690 4 года назад

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.

@user-ey3yn6vu8o 8 месяцев назад

I love you

@kacyk7824 6 лет назад

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

@yvainestelmack7196 2 года назад

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

@katurisuryanarayana9927 4 месяца назад

Example of Williamson synthesis

@keqiangpan5661 3 года назад

i do rate you for boosintg me

@michaeldepauw7446 4 года назад

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!