✦ LIBER ✦

Kinetic evidence for a bimolecular reaction of 2,2-diphenyl-1-picrylhydrazyl with peroxybenzoic acid

✍ Scribed by Katsumi Tokumaru; Takashi Kajiwara; Osamu Simamura

Publisher: Elsevier Science
Year: 1965
Tongue: French
Weight: 152 KB
Volume: 6
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)90108-4

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Reaction of uric acid and 3-N-ribosyluri

Reaction of uric acid and 3-N-ribosyluric acid with 1,1-diphenyl-2-picrylhydrazyl

✍ Robert C. Smith 📂 Article 📅 1982 🏛 Elsevier Science 🌐 English ⚖ 395 KB

Coordination reaction of iron(III) with

Coordination reaction of iron(III) with 8-hydroxy-7[(2-hydroxy-5-carboxyphenyl)Azo]-5- acid: Evidence for kinetic linkage isomerism

✍ Zhi-Ping Bai; Jinsai Hidaka; Hisahiko Einaga 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 490 KB

Chemical, Kinetic, and Spectroscopic Evi

Chemical, Kinetic, and Spectroscopic Evidence for the Reaction of 1-Naphthylcarbene with Acetonitrile to form a Nitrile Ylid.

✍ Robert L Barcus; Bradford B Wright; Matthew S Platz; J.C Scaiano 📂 Article 📅 1983 🏛 Elsevier Science 🌐 French ⚖ 191 KB

The Dimerization of (E)-1,3-Diphenyl-1,3

The Dimerization of (E)-1,3-Diphenyl-1,3-butadiene Proceeds Suprafacially with Respect to Both Components: Evidence for a Concerted [4 + 2] Cycloaddition

✍ Prof. Dr. Johann Mulzer; Dipl.-Chem. Katja Melzer 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 455 KB 👁 1 views

Evidence for a diradical intermediate in

Evidence for a diradical intermediate in the Diels–Alder reaction of 2-butene with cyclohexa-1,3-diene

✍ G. Huybrechts; B. Van Mele 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 English ⚖ 254 KB

Despite an extensive literature, controversy about the Diels-Alder reaction mechanism still exists. For the thermal dimerization of 1,3-butadiene, for example, a concerted one-step [I] or two-stage [2] mechanism, a mixture of orbital symmetry allowed and forbidden cycloadditions 131, as well as a tw

Further evidence for the formation of bu

Further evidence for the formation of butalene in the reaction of 1-chloro-[2.2.0]bicyclohexa-2,5-dienes[dewar chlorobenzenes] with a strong base

✍ Ronald Breslow; Pyare Lal Khanna 📂 Article 📅 1977 🏛 Elsevier Science 🌐 French ⚖ 187 KB

We have described the reaction of 1-chloro-[2.2.0]bicyclohexa-2,5-diene (I) with lithium dialkylamides to afford dialkylanilines. 1 The critical finding with regard to the mechanism of this change is that the reaction of I with lithium dimethylamide in Me2ND in the presence of diphenylisobenzofuran