conversion in amines
just wanna know what happens and the logic between them . and if theres any short trick to do this conversion. thanks
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@Dexter
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Master Organic Chemistry
Reactions of Diazonium Salts: Sandmeyer and Related Reactions
Aromatic amines react with nitrous acid to give diazonium salts. These can undergo further reactions (such as the Sandmeyer reaction) giving useful products
Check diazo coupling
Basically addition of electrophile (here diazonium salt) on the benzene ring, for phenol and aniline, para position coupling is exclusively major pdt, like in this pic, it takes place in mild basic medium, but only for aniline it's mild acidic, they are mild not strong note that, or else for example aniline would take up a hydrogen with it's lone pair in strong acidic medium, which ruins the coupling, these are some basic stuff
sorted?
yes thanks
Nice
+solved @Aguilar
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