𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The Mechanism of the Diazo-Coupling Reaction

✍ Scribed by Hodgson, H. H.


Book ID
115297880
Publisher
Wiley (Blackwell Publishing)
Year
2008
Tongue
English
Weight
550 KB
Volume
58
Category
Article
ISSN
0037-9859

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Mechanisms of Diazo Coupling Reactions.
✍ Richard P. Kelly; John R. Penton; Heinrich Zollinger 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 German ⚖ 591 KB

## Abstract The rearrangements of 4′‐methoxy‐__N__‐methyl‐ and __N__‐methyl‐4′‐nitro‐diatzoaminobenzene have been studied in 20% acetonitrile/aqueous buffers. The reactions are specifically acid catalyzed and involve pre‐equilibrium formation of amine and diazonium salt followed by rate‐limiting at

Preparation of Diazo Phenyl Sulfides. Ki
✍ Alfy Badie Sakla; Nabil Khalil Masoud; Zaki Sawiris; Wagih Sadik Ebaid 📂 Article 📅 1974 🏛 John Wiley and Sons 🌐 German ⚖ 421 KB

## Abstract Aryldiazophenyl sulfides prepared from diazotised arylamines and thiophenol at controlled pH, are coupled with β‐naphthol yielding the corresponding azo dye. A kinetic study of the diazo coupling reaction of __p__‐nitrobenzenediazo phenyl sulfide with β‐naphthol under various condition

Mechanisms of Diazo Coupling Reactions.
✍ John R. Penton; Heinrich Zollinger 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 German ⚖ 615 KB

## Abstract In the title reactions it is shown that aminoazo formation does not occur by direct attack of diazonium ion at C‐atom. Initial attack is at N‐atom, but proton loss from the ω~N~‐complex formed is relatively slow. Hence, at low amine concentration this rearranges intermolecularly to the