The effect of ion pairing on the stereochemistry of elimination from quaternary ammonium salts
โ Scribed by J.K. Borchardt; W.H. Saunders Jr.
- Publisher
- Elsevier Science
- Year
- 1972
- Tongue
- French
- Weight
- 180 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Recent reports have called attention to the importance of ion pairing in determining the stereochemistry of elimination from cycloalkyl tosylates and
๐ SIMILAR VOLUMES
FT-IR. Two types of quaternary ammonium bromides (i.e., [4r4r4r4] and ooctanoic acid; ion-pair association; phase separation pheno-[1r1r1r13]) were used as received from Tokyo Kasei Company and Wako menon. Pure Chemical Company, respectively. Quaternary ammonium bromide aqueous solution 1 mol dm 03
## The ion pair formation between quaternary ammonium ions and various anions was studied by high voltage paper electrophoresis. There seems to be little ion pair formation in 0.1 N solutions but quite considerable interaction in I IV solutions.
266 t?o. 4 trans-and cis-olefin proportions. Therefore, we have now investigated the effect of dicyclohexyl-18-crown-6-ether (N)'\*l\* on the trans-and cis-olefin composition in reaction of the bromide I (X-Br) and the tosylate I (X=OTs) with potassium tert-butoxide in three very different sohrents