Williamson Ether Synthesis
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- Опубликовано: 26 авг 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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one important thing that R-X must be 1 degree or elimination competes over substituion and alkene are formed
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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.
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Hello sir, amazing video! Please could you explain why in the third question you wouldn't get hydrolysis on the chloride?
I think if there's intermolecular shifting possible there's no need of hydrolysis. Moreover it can increase the chances of elimination
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is it possible that ,in the example 3, being a huge cyclic whit one more alcocide?
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is it 1 pot or should you first do the alkoxi?
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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?
Ether =💨 + β ond = more tangible compounds .
Sn2 mechanism
Do you give any courses or only youtube?
Do we have here E2 side reaction?
cheers
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.
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.
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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.
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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