The gas-phase reaction of Cl atoms with benzene has been studied using both
experimental and computational methods. The bulk of the kinetic data were
obtained using steady-state photolysis of mixtures containing Cl-2, C6H6, a
nd a reference compound in 120-700 Torr of N-2 diluent at 296 K. Reaction o
f Cl atoms with C6H6 proceeds via two pathways; (a) I-I-atom abstraction an
d (b) adduct formation. At 296 K the rate constant for the abstraction chan
nel is k(1a) = (1.3 +/- 1.0) x 10(-16) cm(3) molecule(-1) s(-1). Phenyl rad
icals produced via H-atom abstraction from C6H6 react with Cl-2 to give chl
orobenzene. The main fate of the C6H6-Cl adduct is decomposition to reform
C6H6 and Cl atoms. A small fraction of the C6H6-Cl adduct undergoes reactio
n with Cl atoms via a mechanism which does not lead to the production of C6
H5Cl, or the reformation of C6H6. As the steady-state Cl atom concentration
is increased, the fraction of the C6H6-Cl adduct undergoing reaction with
Cl atoms increases causing an increase in the effective rate constant for b
enzene removal and a decrease in the chlorobenzene yield. Thermodynamic cal
culations show that a rapid equilibrium is established between Cl atoms, C6
H6, and the C6H6-Cl adduct, and it is estimated that at 296 K the equilibri
um constant is K-c,K-1b = [C6H6-Cl]/[C6H6][Cl] and lies in the range (1-2)
x 10(-18) cm(3) molecule.(1) Flash photolysis experiments conducted using C
6H6/Cl-2 mixtures in 760 Torr of either N-2 or O-2 diluent at 296 K did not
reveal any significant transient UV absorption; this is entirely consisten
t with results from the steady-state experiments and the thermodynamic calc
ulations. The C6H6-Cl adduct reacts slowly (if at all) with O-2 and an uppe
r limit of k(C6H6-Cl + O-2) < 8 x 10(-17) cm(3) molecule(-1) s(-1) was esta
blished. As part of this work a value of k(Cl + CF2ClH) = (1.7 +/- 0.1) x 1
0(-15) cm(3) molecule(-1) s(-1) was measured. These results are discussed w
ith respect to the available literature concerning the reaction of Cl atoms
with benzene.