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@Dexter
Note for OP
+solved @user1 @user2... to close the thread when your doubt is solved. Mention the users who helped you solve the doubt. This will be added to their stats.Can you elaborate what happen in the step before?
This forms in the first step
This is the final pdt
Okay so this looks like a base. There is a lone pair on N and another coupl3 on O. With H+ (an acid) what could happen?
N is a better base than O, so N takes H+
Wont oxygen take the H+?
it is more electronegative
it also has more free electrons
James Ashenhurst
Master Organic Chemistry
Beckmann Rearrangement
Description: The Beckmann rearrangement is a reaction of oximes that can result in either amides or nitriles, depending on the starting material. (Oximes derived from ketones
here is the whole reaction mechanism :)
OH WAITTT
ITS BECKMAN REARRANGEMENT
Ahh got it got it
Thanks, didn't recognise it before
+solved @iTeachChem
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