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Benzenesulfonate ion

Addition-elimination reactions occur on treatment of 2,3-diphenylthiirene 1,1-dioxide with benzenesulfonate ion or with trisubstituted phosphines (Scheme 86) (75JQC3189). [Pg.161]

Eschenmoser and co-workers have provided strong evidence that the transition state in an Sn2 reaction must be linear. Base treatment of methyl a-tosyl-o-toluenesulfonate (4) gives the o-(l-tosylethyl)benzenesulfonate ion (6). The role of... [Pg.392]

Zinc benzenesulfonate, Zn(C6H5S03)2,6H20, is prepared in aqueous solution and has a structure containing alternate layers of [Zn(H20)6]21 and benzenesulfonate ions. They can be compared to layered metal phosphonates 43... [Pg.1182]

For our example, this means that the benzenesulfonate ions are adsorbed in a surface layer and that the sodium ions form an atmosphere of counter ions in which their concentration gradually decreases with the distance from the benzenesulfonate layer. A small separation between the negative and the positive charges has been created at the interface between the mobile and the stationary phases. As in a plate capacitor, this charge separation creates a difference in electrostatic potential between the charged stationary phase and the surrounding mobile phase. By convention, the surface has a negative electrostatic potential in this case. [Pg.422]

Table I. Equilibrium Constants for Methylation of Benzenesulfonate Ion (KXr) and Identity Rates (k ) for Neutral Methylation Agents in Sulfolane at 35 °C... Table I. Equilibrium Constants for Methylation of Benzenesulfonate Ion (KXr) and Identity Rates (k ) for Neutral Methylation Agents in Sulfolane at 35 °C...
Some interesting consequences of the neglect of the quadratic term result. The equation then becomes equation 4, and when equilibrium constants KXr and KYr with a reference nucleophile (such as benzenesulfonate ion in Table I) are available, we can write... [Pg.45]

These gave good films for the pure polymer and could be used to cast films of the polymer blends. Of the various forms of polyanisidine, those containing the benzenesulfonate ion and the trifluoroacetate ion were soluble in DMF, dimethylsulfoxide (DMSO), and NMP. They were slightly soluble in chloroform, acetonitrile, acetone, methanol, ethanol, ethyl acetate and THF. [Pg.176]

A proton is removed from the arenium ion to form the benzenesulfonate ion. [Pg.683]

The benzenesulfonate ion accepts a proton to become benzenesulfonic acid. [Pg.683]


See other pages where Benzenesulfonate ion is mentioned: [Pg.886]    [Pg.479]    [Pg.886]    [Pg.761]    [Pg.886]    [Pg.886]    [Pg.611]    [Pg.761]    [Pg.485]    [Pg.462]    [Pg.462]    [Pg.917]    [Pg.82]   
See also in sourсe #XX -- [ Pg.917 ]




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