so perfumers should not call the product a schiff base.
i am not confused with the mechanism, i only explained the attack from a primary amine use
the second deprotonation comes from one of the hydrogen electrons in the adjacent carbon, when using a secondary amine
i didnt say your diagram was wrong......
i suppose it might have been much easier to simply say that perfumers
shouldn't call the product in your diagram a schiff base, rather than trying to explain why
that's all ......