-
Hydrolysis (X− = OH−) is a
special case of
protonolysis.
Compounds susceptible to
hydrolysis often undergo protonolysis. The
borohydride anion is susceptible...
-
Preparation of
crystal violet by
protonolysis of the
tertiary alcohol....
- of a
group from
boron to the
electrophilic α position.
Oxidation or
protonolysis of the
resulting organoboranes generates many
organic products, including...
-
reducing agent in
organic synthesis. This
colourless salt is
prepared by
protonolysis of
sodium borohydride with
acetic acid: Na[BH4] + 3 CH3COOH → Na[(CH3COO)3BH]...
-
Trimethylaluminium is one of the
simplest examples of an
organoaluminium compound.
Despite its name it has the
formula Al2(CH3)6 (abbreviated as Al2Me6...
-
carbonyl oxygen,
addition of the
alcohol to the
protonated carbonyl,
protonolysis of the
resulting hemiacetal or hemiketal, and
addition of the second...
-
Sodium borohydride, also
known as
sodium tetrahydridoborate and
sodium tetrahydroborate, is an
inorganic compound with the
formula NaBH4 (sometimes written...
-
ortho product:
Protodeboronation is a
chemical reaction involving the
protonolysis of a
boronic acid (or
other organoborane compound) in
which a carbon-boron...
- TBAF
gives carbanions that can be
trapped with
electrophiles or
undergo protonolysis. Li, ****-Yin; Sun, Haoran; DiMagno,
Stephen G. (2007). "Tetrabutylammonium...
- In
organophosphorus chemistry,
aminophosphines are
compounds with the
formula R3−nP(NR2)n
where R is a
hydrogen or
organic substituent, and n = 0, 1, or...
