- -oʊl/), is a
substituted aromatic hydrocarbon with the
chemical formula C6H5CH3,
often abbreviated as PhCH3,
where Ph
stands for
phenyl group. It is a...
- acid and water, TsOH
undergoes hydrolysis to toluene: CH3C6H4SO3H + H2O →
C6H5CH3 + H2SO4 This
reaction is
general for aryl
sulfonic acids.
Tosyl Collidinium...
-
industrially by the gas-phase
photochemical reaction of
toluene with chlorine:
C6H5CH3 + Cl2 → C6H5CH2Cl + HCl In this way,
approximately 100,000
tonnes are produced...
-
reaction with
ammonia and
oxygen (or air) at 400 to 450 °C (752 to 842 °F).
C6H5CH3 + 3/2 O2 + NH3 → C6H5(CN) + 3 H2O In the
laboratory it can be prepared...
-
benzyl chloride (C6H5CH2Cl) and
followed by
benzotrichloride (C6H5CCl3):
C6H5CH3 + Cl2 → C6H5CH2Cl + HCl C6H5CH2Cl + Cl2 → C6H5CHCl2 + HCl C6H5CHCl2 + Cl2...
- Friedel–Crafts
reaction using AlCl3 as a catalyst, may
produce singly methylated (
C6H5CH3),
doubly methylated (C6H4(CH3)2), or
still more
highly methylated (C6H6−n(CH3)n)...
- (M = Ti, Zr, Hf, Mo or W; cp = cyclopentadienyl, η5-C5H5) or [AgOTeF5-(
C6H5CH3)2]2. In the
actinide series,
uranyl compounds such as
uranyl chloride (UO2Cl2)...
- hydrogenolysis: C6H5CH2NH2 + 2 RBr → C6H5CH2NR2 + 2 HBr C6H5CH2NR2 + H2 →
C6H5CH3 + R2NH
Typically a base is emplo**** in the
first step to
absorb the HBr...
-
industrially as a
byproduct of the
dealkylation of
toluene to
produce methane:
C6H5CH3 + C6H6 → C6H5−C6H5 + CH4 The
other prin****l
route is by the oxidative...
- and methane: C 6 H 5 CH 3 + H 2 ⟶ C 6 H 6 + CH 4 {\displaystyle {\ce {
C6H5CH3 + H2 -> C6H6 + CH4}}} This
irreversible reaction is
accompanied by an equilibrium...
