Steric effect of o-methyl groups on the ionization constants of phenols. The influence of the solvent
โ Scribed by C. L. de Ligny
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 126 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0165-0513
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The alkyIation of enaminoltetones, I. warr reported by Leonad and Adamcik 1.2 to give rise too-alkylated salts, II. The latter was found to be readily displaced by nucleophiles (amines, thiola, etc. ) at the ring carbon to give a variety of substituted iminium salts, III. Ia a program a-d at studyin
longer of thrend-like shnpe niid hencc the viscosities of aqueous solutions of low-moleculnr starches will not follow Stnudingcr's rnlc. (3) The abore diKerences between solutions of highand lorn-molecular stnrclics linre been erplnined on the basis of t.hc structure of tlic starch nincromolcculc r
With a rlew to syntheslsing trarrs lactones of the desmotroposantonln series, van Tamelen and his associates' studied the Interactions of the anions generated from diethyl malonate and dlethyl methylmalonate with the epoxlde(T) in refluxing ethanolic solution. The lactonic products thus isolated wer