An ammonium imine is another name for amine imide - any of a class of organic compounds formally derived from an amine and a nitrene - of general formula R3N+-N-R..
due to the imine bond
ammonium perchlorate
ammonium hydroxide, ammonium nitrate, ammonium sulphate, uranium diuranate, ammonium chloride, ammonium carbonate, ammonium fluoride, ammonium bromide, etc.
Formaldehyde when reacted with glycine in a completely neutral solution forms CH2NCH2COO- imine. The formation of this imine permanently blocks the completely ampholytic nature of glycine in an acid solution, when otherwise it would have formed HOOC-CH2-NH3+. Here both the solutions of formaldehyde as well as glycine have to be completely neutral or slightly basic , to ensure that all NH2 gets converted to imine.
Ammonium Chloride
An acyliminium is an acyl iminium ion - an ion of iminium, a form of quaternary ammonium formed by an imine.
Yes. Imine is derived from ammonia and containing an NHgroup attached by a double bond to a carbon atom in another group.
An imine is a functional group or chemical compound containing a carbon-nitrogen double bond. An imine can be synthesised by the nucleophilic addition of an amine to a ketone or aldehyde giving a hemiaminal -C(OH)(NHR)- followed by an elimination of water to yield the imine. However, the equilibrium in this reaction usually lies in favor of the free carbonyl compound and amine, so that azeotrope distillation or use of a dehydrating agent such as molecular sieves is required to push the reaction in favor of imine formation. For more details, see the links on the left side of this column.
due to the imine bond
ammonium perchlorate
Iminazole, iminent, iminourea, imine, and imino.
An aldimine is an imine derived from an aldehyde, with a general formula RCH=NR.
ammonium hydroxide, ammonium nitrate, ammonium sulphate, uranium diuranate, ammonium chloride, ammonium carbonate, ammonium fluoride, ammonium bromide, etc.
Formaldehyde when reacted with glycine in a completely neutral solution forms CH2NCH2COO- imine. The formation of this imine permanently blocks the completely ampholytic nature of glycine in an acid solution, when otherwise it would have formed HOOC-CH2-NH3+. Here both the solutions of formaldehyde as well as glycine have to be completely neutral or slightly basic , to ensure that all NH2 gets converted to imine.
Ammonium bisulfite is NH4HSO3 Ammonium bisulfide is NH4SH Ammonium bisulfate is NH4HSO4
it is a base because of its weak basic imine group
NH4Cl is ammonium chloride.