Benzene/EAS Complete the Reaction and Synthesis Examples
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- เผยแพร่เมื่อ 13 ต.ค. 2024
- joechem.io/vid... for video on jOeCHEM and attached worksheet + solution (below video on jOeCHEM aka the link)
Worksheet: worksheets.joec...
Worksheet Solution: worksheets.joec...
Worksheet Solution Walkthrough: joechem.io/vid...
Study Guide: (To be created, but Joe's working on it!)
In this video, we do synthesis practice with benzene and EAS reactions.
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This was loki actually rlly helpful.
good video bro but at the end w the synthesis i didnt understand the need for protecting the NH2 and reacting with SO3, i thought i could just add a acid chloride ortho to the benzene with NH2 and be chilling
hey @smalliver365! First off, thanks for watching and the kind words.
So it *is* necessary because of the strong basic character of the -NH2 group. Feel free to give this video section a watch (th-cam.com/video/Xvt6yAqwsQ8/w-d-xo.htmlsi=HRmo3kjeg3jhc0rT&t=391), but the short summary is that whenever you expose an -NH2 group to acidic conditions, the very basic nitrogen in the NH2 will be tempted to grab H+, thus transforming the group into an ammonium ion aka -NH3+.
Once the -NH2 group gets protonated and becomes -NH3+, you now have a deactivating, meta director group. So you have to be careful when you have an -NH2 group, so protecting it helps make it LESS basic, allows you to safely introduce acidic conditions for adding the SO3 group, and then you can deprotect it.
After adding NH2 in the benzene ring, would I be wrong to just go straight to sulfonation then acylation and add H3O to remove the SO3H group.
If you go with the sulfonation first, you're going to introduce an acidic environment to the NH2 group, which is basic. The NH2 will be tempted and grab H+, turning it into NH3+, and effectively becoming a deactivating meta group. So I would avoid doing that.
Why would the water molecule not act as the nucleophile when the carbocation is formed?
Hey Mckaila! Which problem are you referring to? If you could provide a time in the video that would also be helpful (also, thanks for watching!)
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