Williamson ether synthesis | Organic chemistry | Khan Academy
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- čas přidán 7. 09. 2024
- Two-step synthesis of an ether from an alcohol, A strong base is a dded to deprotonate the alcohol, which then attacks an alkyl halide. Created by Jay.
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Organic Chemistry on Khan Academy: Carbon can form covalent bonds with itself and other elements to create a mind-boggling array of structures. In organic chemistry, we will learn about the reactions chemists use to synthesize crazy carbon based structures, as well as the analytical methods to characterize them. We will also think about how those reactions are occurring on a molecular level with reaction mechanisms. Simply put, organic chemistry is like building with molecular Legos. Let's make some beautiful organic molecules!
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you make organic chem a piece of cake. god bless you
Brilliantly explained! Very easy to understand the basic concept! Thank you!
clear, concise, and much better than my Prof.'s explanation. well done sir and thank you
thank you, this was very helpful!
Thank you so much !
I have an exam today, and this really helped :)
Understood 100%
Slow down, good sir.
Sn2 also depends on nucleophile right? Then if we have a bulky alkoxide it will be less nucleophilic, in that case chances of sn2 should decrease right?
very good one
Thanks so much this is awesome.
Thanks!
Thank you
this is really awesome
thanks
Thank you tremendously! Such a good explanation!\
Awesome!!!
Nerolin is ethoxy, not methoxy, right?
Is this willimson synthesis? but where as in our text book it is written as alkyl halide reacts with sodium or potassium alkoxide to give a ether.but what u say is quite different from the textbook.Im in confusion
Have any of you used Numerade?
if we use 3rx what the mechanism ??
nice explanation but talk a bit slow
Intentionally
like that
You spoke rather quickly. It was a bit hard to keep up with you.