| Bulletin of the Korean chemical society | |
| Correlation of the Rates of Solvolysis of Phenyl Chlorodithioformate | |
| Jin Soon Yang1  In Sun Koo1  T. W. Bentley1  Jun Mi Cho1  Ikchoon Lee1  Kiyull Yang1  Sun Kyoung An1  Jong Pal Lee1  | |
| 关键词: Chlorodithioformate; Ionizing power; Nucleophilicity; Solvolysis; | |
| DOI : | |
| 学科分类:化学(综合) | |
| 来源: Korean Chemical Society | |
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【 摘 要 】
Solvolytic rate constants at 25 �? are reported for solvolysis of chlorodithioformate (1) in binary mixtures of water with acetone, ethanol, methanol, methanol-d, 50%methanol-d/50%D2O, and 2,2,2-trifluroethanol (TFE), and also in TFE-ethanol mixtures. The Grunwald-Winstein plot shows that the three aqueous mixtures exhibit dispersions into separate line. The correlation is improved only slightly by additional parameters NT for solvent nucleophilicity and/or I for aromatic ring parameter. Rate ratios in solvents of the same YCl value, having different nucleophilicity provide measures of the minimum extent of nucleophilic solvent assistance, and the value of 3.35 for [k40EW/k97TFE]Y (EW = ethanol-water), is consistent with an essentially SN1 reaction mechanism. This study has shown that the magnitude of l, m and h values associated with a change of solvent composition is able to predict the SN1 reaction mechanism. log(k/ko) = mY + lN + hI
【 授权许可】
Unknown
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO201912010238371ZK.pdf | 103KB |
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