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Negatively charged species

It will become apparent that fluorine not directly attached to the carbanionic carbon 1.18B is strongly stabUising but, when directly attached as in 1.18A and 1.19A, it has either a moderate stabilising effect compared with hydrogen, or it definitely destabilises, depending on the stereochemistry of the carbanion. [Pg.16]

in MO terms, this would be described as interaction of the filled p-orbital on carbon with ct -orbitals associated with C—F bonds. [Pg.16]


Solvent Effects on the Rate of Substitution by the S l Mechanism Table 8 6 lists the relative rate of solvolysis of tert butyl chloride m several media m order of increasing dielectric constant (e) Dielectric constant is a measure of the ability of a material m this case the solvent to moderate the force of attraction between oppositely charged par tides compared with that of a standard The standard dielectric is a vacuum which is assigned a value e of exactly 1 The higher the dielectric constant e the better the medium is able to support separated positively and negatively charged species 8olvents... [Pg.345]

Putting it another way, the adds in successive steps become progressively weaker. This is reasonable it should be more difficult to remove a positively charged proton, H+, from a negatively charged species like H2P04- than from a neutral molecule like H3PO4. [Pg.367]

These arise either by an analogous process to that described above for Cl, i.e. the adduction of a negatively charged species such as Cl , and the abstraction of a proton to generate an (M — H) ion, or by electron attachment to generate an M ion. The ions observed in the mass spectrum are dependent on the species generated by the reagent gas and the relative reactivities of these with each other and with the analyte molecule. [Pg.56]

Neutral atoms or molecules can also capture electrons, producing negatively charged species, which scientists distinguish from their neutral counterparts by adding superscript minus signs to the chemical symbols ... [Pg.103]

The first step is so fast that it can hardly be measured experimentally, while the second step is much slower (probably as a result of the repulsion of negatively charged species, R and R2-, in the negatively charged diffuse electric layer). The reduction of an isolated benzene ring is very difficult and can occur only indirectly with solvated electrons formed by emission from the electrode into solvents such as some amines (see Section 1.2.3). This is a completely different mechanism than the usual interaction of electrons from the electrode with an electroactive substance. [Pg.396]

Negatively charged species such as carboxylic acid group in acid-treated CNTs can attract positively charged enzymes from solution as long as the pH value of the enzyme solution is controlled to be lower than the iso-electric point of the enzyme thus, multilayer films of the enzyme can be formed by the layer-by-layer technique. For example, five layers of GOx can be immobilized on the electrode surface by alternatively dipping a poly(diallyldimethylammonium chloride (PDDA))-functionalized GC into a CNT solution and a GOx solution (pH 3.8). Figure 15.15 illustrates the preparation process for the formation of a multilayer film of GOx on the electrode. [Pg.502]

Bacteria that live in the dark must derive the free energy to move electrons around in chemistry and a series of reactions based on the iron pyrite surfaces have been shown to be exoergic (Figure 9.13). The cationic pyrite surface serves as the catalyst for the binding of negatively charged species, perhaps tagged with... [Pg.278]

This is exactly the same as the experimental rate law. It is reasonable that the first step be slow since it involves two negatively charged species coming together. We know that like charges repel, and thus this should not be an easy or rapid process. [Pg.339]

A negatively charged species will attract a positively charged proton and act as a base. [Pg.366]

Although interesting, the anion-molecule interactions have not been treated as extensively by ab initio methods as cation-molecule interactions. This may be partially due to convergence difficulties which frequently arise in H. F. calculations including negatively charged species. The only anions discussed in some detail are... [Pg.85]

As noted earlier, positively charged species such as the ammonium ion, NH4+, are known as cations and negatively charged species such as the chloride ion, Cl , are known as anions. The point here is that spermidine (and putrescine and cadaverine) is a base that is, it has the capacity to add a proton. In fact, it has three sites to which a proton might be added, the three amino nitrogen atoms. In principle, it could add three protons and end up with three positive charges. In fact, under the conditions of most living cells, it adds two protons and exists as a dication (dye-cation) ... [Pg.71]


See other pages where Negatively charged species is mentioned: [Pg.79]    [Pg.219]    [Pg.516]    [Pg.1500]    [Pg.380]    [Pg.593]    [Pg.210]    [Pg.214]    [Pg.88]    [Pg.398]    [Pg.99]    [Pg.131]    [Pg.64]    [Pg.212]    [Pg.41]    [Pg.567]    [Pg.8]    [Pg.807]    [Pg.369]    [Pg.189]    [Pg.279]    [Pg.283]    [Pg.201]    [Pg.36]    [Pg.161]    [Pg.402]    [Pg.107]    [Pg.50]    [Pg.950]    [Pg.228]    [Pg.166]    [Pg.298]    [Pg.20]    [Pg.203]    [Pg.64]    [Pg.54]    [Pg.425]   


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Charged species

Negative charge

Negatively charge

Negatively charged

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