Gencralizcd Hartrce-Fock (CHF) calculations Indicate that the aromatic substitutiou reaction kr the ground state CXI bc classified into three types: (A) nonradical ionic (S N2, SE2) reaction, where the closed-shell character is always retained; (B) electron-transfer type I (ET I) reaction, where the
Mechanisms of substitution reactions of pentacyanoaquocobaltate (III)
β Scribed by L. Viaene; J. D'Olieslager; S. De Jaegere
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Weight
- 490 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0037-9646
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β¦ Synopsis
Abstract
The thermal and the photochemical reactions of Co(CN)~5~H~2~O^2β^ with azide, iodide, hydroazoic acid and hydrocyanic acid are investigated. Data on the photochemical aquation of Co(CN)^3β^~6~ as a function of the chemical properties of the medium are also reported. On the basis of these kinetic data a reaction mechanism is proposed which takes into account the important role of the solvent cage surrounding the reacting complex.
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The reactions of 4-(4'-nitrophenyl)-4-X-butan-2-one (1-X; X = Cl, OTs) with added bases/nucleophiles exhibit second-order kinetics. These substitution and elimination reactions are concluded to be of concerted S N 2 type and irreversible E1cB type, respectively. The spontaneous formation of alkene f
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