>>11618856Maybe it can happen, but it sure as shit ain't favorable.
Carbanions don't form on their own spontaneously, they need strong bases, even in conjugated systems. You also draw the carbanion next to an oxygen, this is unfavorable as oxygen in electron donating and thus prefers to form a carbonyl.
The way you draw your arrows makes no fucking sense. You draw them moving towards each other, by doing so your imply that electron pairs are moving towards each other. Classical physics tells us that two negatively charged objects repel. Also how the fuck does,what I assume is a primary amide, have a positive charge under basic conditions ?
This whole fucking page is a mess m8. It breaks both chemical conventions and common sense.