Williamson Ether Synthesis
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- čas přidán 30. 07. 2024
- We know what ethers are, so now let's go over one very simple way to make them. That's the Williamson Ether Synthesis. It's pretty much just SN2, so let's check it out!
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Please do more Organic Chem 2 reactions. Your videos are so much more clear than our lectures. Seems like you're speaking English, and my professor is speaking Chinese.
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You uploaded just in time 😆We just started studying about ethers so this will help a lot!
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No way. It can't be this simple :O I thought this synthesis was very hard to understand until I watched your video.
fantastic
Hello sir, amazing video! Please could you explain why in the third question you wouldn't get hydrolysis on the chloride?
is it possible that ,in the example 3, being a huge cyclic whit one more alcocide?
Thank you for you video! I have a question on the 3. Example. I paused the video to solve it by myself. And i wanted to ask you, if it is possible to get an NaCl as a sideproduct instead of Cl- just leaving?
one important thing that R-X must be 1 degree or elimination competes over substituion and alkene are formed
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is it 1 pot or should you first do the alkoxi?
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Do we have here E2 side reaction?
What exactly is the role of the water in the third example reaction? It's not really participating in the reaction, is it? So wouldn't the same reaction also take place in a non-aqueous system?
This is a great question that I think Leah4Sci helped to answer for me. I think the idea is that if your solvent is the conjugate acid of the Nphile/Base, then it doesn’t solvate said molecule too much. But it can still stabilize carbocations and whatnot. Weigh in Davedawg?
h2o is the product of OH- attacking the alkoholic group.
In the 3rd problem,will the -OH displace-Cl by sn2 since it's a strong base and primary alkyl halide?
Very strong base, will do acid-base reaction much faster than coordinating.
Thank you so much sir
Why doesn't the Na+ ion react to the O- part of the hydrocarbon in the beginning???
It'll hang out by the oxyanion until it reacts.
I am a simple student who cheated his way out of grade 11 and grade 12. You're helping me in my university exams now lol
Hi
Sn2 mechanism
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Is possible to make ether from alkyl halide?
that's what would be explained in this video you're commenting on.
Ether =💨 + β ond = more tangible compounds .
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Good morning form Queensland Australia 30AUG2018
So if I drink it I’ll smell like it? So just huff you say?
Wrong ether? Dam I’m over here trying to meme and I’m learning like a nerd
You ether get it or you don't I guess.
I think it's not hard to not able to guess it
By - Williamson