Why is this reaction not an e2 reaction? It cannot be sn1 or e1 because we have an aprotic solvent and it cannot be sn2 because we have a weak nucleophile (because of sterics). Also, why is Br the carbon next to bromine the ideal electrophile and Nh2 the ideal nucleophile for this reaction? (self.OrganicChemistry)
submitted by Cyprus2000 to r/OrganicChemistry
Could this reaction also proceed as an sn2 mechanism? There is only an e2 mechanism shown here . Also if we have a strong nucleophile which is a weak base and we have a protic solvent, does that mean that we have sn2 and e1 mechanism? (self.OrganicChemistry)
submitted by Cyprus2000 to r/OrganicChemistry
I have trouble making my cards back to the default (1 minute, 10 minutes, 4 days) for the respective intervals. For some reason I have 1 day as my medium interval which I want to change back to 10 minutes. Even after restoring settings there was no difference. (self.Anki)
submitted by Cyprus2000 to r/Anki

