## Abstract The following reactions have been studied kinetically: 1. Solvolysis of 1‐, 3‐ and 8‐chloromethylfluoranthene with (a) water 20,5%‐dioxane 79,5%, (b) water 6,1%‐dioxane 39,8%‐formic acid 54,1%.
Etudes cinétiques dans le domaine des dérivés polycycliques aromatiques. X. Application de la méthode des orbitales moléculaires à l'étude de la réactivité de dérivés chlorométhylés du fluoranthène
✍ Scribed by G. Geuskens; G. Klopman; J. Nasielski; R. H. Martin
- Publisher
- John Wiley and Sons
- Year
- 1960
- Tongue
- German
- Weight
- 283 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The potential barriers of some nucleophilic substitutions have been estimated by simple LCAO‐MO treatment.
📜 SIMILAR VOLUMES
## Abstract ARRHENIUS parameters have been determined for the solvolysis of a series of acid chlorides of polycyclic aromatic hydrocarbons in methanol‐acetone (1:1) (Table 11). The fact that the solvolyses were carried out at an average temperature (275°K)situated above the isokinetic temperature (
## Abstract ARRHENIUS parameters have been determined (a) for the solvolysis of 1‐,3‐ and 4‐chloromethylpyrene in different solvents (Table 11) and (b) for the S,2 reaction of 1‐ and 4‐chloromethylpyrene with KI in acetone (Table IV). Taking into account previous results, it is shown that 3‐chlorom
## Abstract Les paramètres d'__Arrhenius__ de l'hydrolyse par la soude caustique, dans l'éthanol à 85%, des esters suivants: benzoate d'éthyle, naphtoates‐1 et ‐2 d'éthyle, phénanthroates‐9, ‐2 et ‐3 d'éthyle et anthroate‐9 d'éthyle ont été déterminés.