- -oʊl/), is a
substituted aromatic hydrocarbon with the
chemical formula C6H5CH3,
often abbreviated as PhCH3,
where Ph
stands for the
phenyl group. It is...
- acid and water, TsOH
undergoes hydrolysis to toluene: CH3C6H4SO3H + H2O →
C6H5CH3 + H2SO4 This
reaction is
general for aryl
sulfonic acids.
Tosyl Collidinium...
- 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)...
-
industrially by the gas-phase
photochemical reaction of
toluene with chlorine:
C6H5CH3 + Cl2 → C6H5CH2Cl + HCl In this way,
approximately 100,000
tonnes are produced...
-
these conditions,
toluene undergoes dealkylation to
benzene and methane:
C6H5CH3 + H2 → C6H6 + CH4 This
irreversible reaction is
accompanied by an equilibrium...
-
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...
- (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)...
-
benzyl chloride (C6H5CH2Cl) and
followed by
benzotrichloride (C6H5CCl3):
C6H5CH3 + Cl2 → C6H5CH2Cl + HCl C6H5CH2Cl + Cl2 → C6H5CHCl2 + HCl C6H5CHCl2 + Cl2...
-
chlorine radical converts toluene to the
benzyl radical: Cl2 + hν → 2 Cl·
C6H5CH3 + Cl· → C6H5CH2· + HCl C6H5CH2· + Cl· → C6H5CH2Cl
Mercaptans can be produced...
- hydrogen) on an
aromatic ring is oxidized, e.g.
toluene to
benzoic acid. 5
C6H5CH3 + 6 KMnO4 + 9 H2SO4 → 5 C6H5COOH + 14 H2O + 3 K2SO4 + 6 MnSO4
Glycols and...
