I need help figuring out the mechanism with which aldahydes and ketones oligermize when the imine is being synthesized via ammonia ...for example formaldahyde and ammonia oligermizes to hexamine
specifically im looking for the oligermized product of ammonia and acetone ..and the relative stabilty of the imine formed previous to the oligermization because i need the imine for sythesis of another compound
Thanks
Mina