Kinetics and Mechanism of the Reaction of Benzoyi Chloride with 4-(4’-N,N-Dimethylaminostyryl)pyridine N-Oxide in Acetonitrile

doi:10.1070/MC1995V005N04ABEH000507

Paper

Kinetics and Mechanism of the Reaction of Benzoyi Chloride with 4-(4’-N,N-Dimethylaminostyryl)pyridine N-Oxide in Acetonitrile

Published 1995 · G. D. Titskii, M. K. Turovskaya, A. Yakovets

Mendeleev Communications

Q3 SJR score

2

Citations

0

Influential Citations

Full textSemantic Scholar

Abstract

The reaction of benzoyl chloride with 4-(4′-N,N-dimethylaminostyryl)pyridine-N-oxide in toluene proceeds according to an addition—elimination mechanism. The rate and equilibrium constants of the individual steps were determined. An inhibiting effect of the substrate was detected.

Study Snapshot

The reaction of benzoyl chloride with 4-(4′-N,N-Dimethylaminostyryl)pyridine-N-oxide in toluene follows an addition-elimination mechanism, with the substrate showing an inhibitory effect.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Sign up to use Study Snapshot

Consensus is limited without an account. Create an account or sign in to get more searches and use the Study Snapshot.

Create an account

Kinetics and Mechanism of the Reaction of Benzoyi Chloride with 4-(4’-N,N-Dimethylaminostyryl)pyridine N-Oxide in Acetonitrile

Sign up to use Study Snapshot

References

Citations