The rates of formation and yields of products from the dediazoniation of p-nitrobenzenediazonium tetrafluoroborate (PNBD) in aqueous solutions over a range of HCl, NaCl and CuCl 2 concentrations at 60 °C were examined. Two main products were observed: p-nitrophenol (ArOH) and p-nitrochlorobenzene (A
Electrochemical determination of rate constants and product yields for the spontaneous dediazoniation of p-nitrobenzenediazonium tetrafluoroborate in acidic aqueous solution
✍ Scribed by Ma Emma Romero-Nieto; Carlos Bravo-Díaz; Beatriz Malvido-Hermelo; Elisa González-Romero
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 288 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
✦ Synopsis
We have examined the kinetics and mechanisms of the dediazoniation of p-nitrobenzenediazonium tetrafluoroborate in acidic aqueous solutions by employing differential pulse polarography (DPP) and differential pulse voltammetry (DPV) on a glassy carbon electrode combined with the use of a coupling reaction to quench unreacted p-nitrobenzenediazonium ion. These electrochemical techniques show an effective sensitivity and selectivity for detecting arenediazonium ions and arenedediazoniation products under the appropriate experimental conditions (pH, solvent, electrolyte), which allows simultaneous monitoring of the rates of arenediazonium ion loss and product formation and determination of product yields.
📜 SIMILAR VOLUMES