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.

Free Radical Reactions:

Reactions Summary:

Organic Chemistry 1 Final Exam Review:

IR Spectroscopy:

Mass Spectrometry:

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Proton NMR Spectroscopy:

Carbon-13 NMR Spectroscopy:

Ethers and Epoxides:

Diels Alder Reaction:

Organic Chemistry 2 Final Exam Review:
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thank you for teaching what my professor is supposed to be teaching... self-teaching organic thru online classes is hard :/

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

omarmikha
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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.☺

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

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

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

SonuKumar-mesw
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Favoulus explanation deserves to be best organic chemistry tutor

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

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

rebeccaly
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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

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

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

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

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

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

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

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

mahmoudtony
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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

islamicbrotherhood
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write reaction mechanism for benzyl-tert-butyl ether

clementchileshe
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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?

mohamedstes