-
bases than
aliphatic amines.
Aniline reacts with
strong acids to form the
anilinium (or phenylammonium) ion (C6H5−NH+3). Traditionally, the weak basicity...
-
Anilinium chloride is the
organic compound with the
formula C6H5NH+3Cl−. A
white solid, it is the
chloride salt of
anilinium,
which is the
conjugate acid...
-
synthesis of this compound.
Direct nitration of
aniline is
inefficient since anilinium is
produced instead.
Nitration of
acetanilide gives only
traces of 2-nitro...
- in
equilibrium with the more
abundant but less
reactive (deactivated)
anilinium ion (ArNH3+),
which may
explain this
reaction product distribution. According...
-
dehydrates to the sultam. Via the
Bucherer reaction,
heating periacid with
anilinium salts gives the N-phenyl derivative,
precursor to Acid Blue 113. Gerald...
- hydrazinium, or diazanium, H2N−NH+3 (protonated hydrazine, a.k.a. diazane)
anilinium (a.k.a. phenylammonium), C6H5−NH+3 (protonated aniline, a.k.a. phenylamine...
- 230 nm, but in
dilute aqueous acid λmax is 203 nm. In the
latter case the
anilinium cation is
formed and the lone pair is no
longer available for conjugation...
- used due to the
reactivity of aniline. (i.e. It can be
protonated to
anilinium or
oxidized easily.)
Instead the
acetyl protection should be used. Compared...
-
ethylenediamine salt; Mo 4O2− 13 in the pot****ium salt; Mo 5O2− 16 in the
anilinium (C 6H 5NH+ 3) salt; Mo 6O2− 19 (hexa-molybdate) in the tetramethylammonium...
- Busseron, E. (2008). "A New
Glycorotaxane Molecular Machine Based on an
Anilinium and a
Triazolium Station". Chem. Eur. J. 14 (16): 4784–4787. doi:10.1002/chem...
