fn the classic lmestigations of C. K. Ingold and MS coworke~3~, solvolysis of benzbydryl type halides in aqueous acetone was interpreted with the sid of only Olle variety of C8fbOAiMil ion irIteI?x?diate, the ais-8OCi8ted cation, R 83 , at3 in equation (1). In the m-called me8 law effect ROK (canon
Racemization and radio-chloride exchange of p-chlorobenzhydryl chloride in acetone
โ Scribed by S. Winstein; John S. Gall
- Publisher
- Elsevier Science
- Year
- 1960
- Tongue
- French
- Weight
- 369 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Inreamxugmieut, exchange and solwlyeis reactions of neutral organic eubstratee proceeding by way of carbouium ions, it is important to dietiuguishbetweeniouiaatiou and dissociation and to consider explicitly the role of different ionic intermediates representing various stages of ioni~atiou-dieaociatiou2*3. In fact, a coueiderable body of iufonuation is now available anthe intimate couree of carboniumion reactions of allyllc,hoBMllylic~variouerat~~~~giag~t~ 2~3. we have now compare6 the rate6 of racemisation and radio-chloride exchange of pchlorabenshydrglchlorideinacetone rolvent. Three differ by a eubetantial factor and therefore give ccneiderable ineight into the behavior of the ionic intermediates inwlved.
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