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Bulletin of the Korean Chemical Society (BKCS)

ISSN 0253-2964(Print)
ISSN 1229-5949(Online)
Volume 18, Number 11
BKCSDE 18(11)
November 20, 1997 

Mechanism for the Reaction of Substituted Phenacyl Arenesulfonates with Substituted Pyridines under High Pressures
Heon-Young Park, Ki-Joo Son, Duck-Young Cheong, Soo-Dong Yoh*
The rates for the reaction of (Z)-phenacyl (X)-benzenesulfonates with (Y)-pyridines in acetone were measured by an electrical conductivity method at 1-2000 bars and 45 ℃. The magnitudes of the Hammett reaction constants, ρX, ρY and ρZ, represent the degree of Nu-C bond formation and that of C-L bond breaking. The magnitude of correlation interaction term ρij can be used to determine the structure of the transition state (TS) for the SN reaction. As the pressure is increased, the Hammett reaction constants, ρX,
1179 - 1182
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