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Historical developments groups

Carbonyl reactions are extremely important in chemistry and biochemistry, yet they are often given short shrift in textbooks on physical organic chemistry, partly because the subject was historically developed by the study of nucleophilic substitution at saturated carbon, and partly because carbonyl reactions are often more difhcult to study. They are generally reversible under usual conditions and involve complicated multistep mechanisms and general acid/base catalysis. In thinking about carbonyl reactions, 1 find it helpful to consider the carbonyl group as a (very) stabilized carbenium ion, with an O substituent. Then one can immediately draw on everything one has learned about carbenium ion reactivity and see that the reactivity order for carbonyl compounds ... [Pg.4]

The historically developed nomenclature of the compounds classified as the bornane group in this report contributes much more confusion to the terpene literature than the common tetpene names of the compounds belonging to the thujane, carane, and pinane groups. Campbane (Formula 75, Chart 13) is a logical name for the saturated parent hydrocarbon of camphor, which differs from this parent only in that it has an oxo group instead of two hydrogens attached to ring carbon No. 2. [Pg.52]

Grubbs group [31, 32] developed another type of Ni-based catalyst. This neutral Ni-catalyst, based on salicylaldimine ligands, is active in ethene polymerisation without any co-activator and originated from the Shell higher olefin process (SHOP). Shortly thereafter another active neutral P,0-chelated nickel catalysts for polymerisation of ethene in emulsion was developed by Soula et al. [33, 34, 35]. The historical development of single site catalysts is represented in Fig. 1. [Pg.3]

The book is designed to introduce fundamental knowledge in three areas the history of the atom, the periodic table and radioactivity. We will study the historical development of atomic structure theories, the tendencies of elements in periods and groups, and the types of emissions and uses of radioactivity. [Pg.3]

Although the concept of pharmacophores constituting a simple representation of molecules and chemical groups in certain order was introduced nearly a century ago [1], there has been increasing interest and focus on pharmacophores in recent years following the advances in computational chemistry research. The historical development of the pharmacophore concept has recently been reviewed [2],... [Pg.18]

So far the historical development of ionic liquids has mainly been driven by combining imidazolium, pyridinium, ammonium and phosphonium cations with different classes of anions. Chloroaluminate ionic liquids were the first more detailed studied ionic liquids. As early as 1948 they were synthesized by Hurley and Wier at the Rice Institute in Texas as bath solutions for electroplating aluminum [1], Later in the seventies and eighties, these systems were further developed by the groups of Osteryoung [2], Wilkes [3], Hussey [4] and Seddon [4c, 5], Due to their chemical nature, chloroaluminate ionic liquids must be classified as extremely hygroscopic and labile towards hydrolysis. [Pg.105]

A symposium in print, Physical Organic Chemistry for the 21st Century, has appeared under the auspices of IUPAC Commission III.2.439 Some twenty distinguished authors or groups of authors have tried to foresee the way in which the various parts of the subject may develop in the next decade or so. Tidwell has provided a prologue on the first century of physical organic chemistry and many of the articles reflect on the historical development of the subject. [Pg.120]

The historical development of the chemistry of organosilicon compounds is closely related to organometallic chemistry. In Bansen s laboratory about the middle of the nineteenth century, Frankland was investigating the reactions of C2HsI with Zn to withdraw the iodine from the C2H5I and form free C2H5 radicals. The product formed was diethyl zinc. It was soon discovered that an ethyl group could be transferred to other elements from this compound if the reaction were favored by the formation of a salt. [Pg.46]


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