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Group 15 atoms reaction mechanisms

Our first three chapters established some fundamental principles concerning the structure of organic molecules and introduced the connection between structure and reactivity with a review of acid-base reactions In this chapter we explore structure and reactivity m more detail by developing two concepts functional groups and reaction mechanisms A functional group is the atom or group m a molecule most respon sible for the reaction the compound undergoes under a prescribed set of conditions How the structure of the reactant is transformed to that of the product is what we mean by the reaction mechanism... [Pg.142]

According to the mechanism cited, it is easy to understand why polyethylsiloxane is more easily destroyed than polymethylsiloxane the -CH2- group of the ethyl radical and the silicon atom is oxidized more readily than the CH3-group. This reaction mechanism permits us to predict the thermal stability of polyorganosiloxanes on the basis of the structure of the organic radical or group at the silicon atom. [Pg.302]

After deposition of 0.5 nm of copper onto plasma modified polyimide, the peaks due to carbon atoms C8 and C9 and the oxygen atoms 03 and 04 were reduced in intensity, indicating that new states formed by the plasma treatment were involved in formation of copper-polyimide bonds instead of the remaining intact carbonyl groups. Fig. 28 shows the proposed reaction mechanism between copper and polyimide after mild plasma treatment. [Pg.277]

Several distinct mechanisms are possible for aliphatic nucleophilic substitution reactions, depending on the substrate, nucleophile, leaving group, and reaction conditions. In all of them, however, the attacking reagent carries the electron pair with it, so that the similarities are greater than the differences. Mechanisms that occur at a saturated carbon atom are considered first. By far the most common are the SnI and Sn2 mechanisms. [Pg.389]


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