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General Controls on Natural Water Chemistry

General Controls on Natural Water Chemistry Chap. 8... [Pg.268]

General Controls on Natural Water Chemistry Chap. 8 TABLE 8.10 Composition of brine in sandstones A and B in 1968 before deep-well injection, and in 1989 after both have been affected by the injection ... [Pg.300]

In the early 1960s, seminal work by Jencks and coworkers demonstrated that formation and hydrolysis of C=N bonds were proceeding via a carbinolamine intermediate, thus leading to a more general mechanism of addition reactions on carbonyl groups [17-19]. The dynamic nature of the reaction of imine formation can be exploited to drive the equilibrium either forward or backwards. Since the reaction involves the loss of a molecule of water, adding or removing water from the reaction mixture proved an efficient way to shift the equilibrium in either direction. The responsive behavior of imines to external stimuli makes the reversible reaction of imine formation perfectly suited for DCC experiments [20], Thermodynamically controlled reactions based on imine chemistry include (1) imine condensation/hydrolysis, (2) transiminations, and (3) imine-metathesis reactions... [Pg.294]


See other pages where General Controls on Natural Water Chemistry is mentioned: [Pg.266]    [Pg.266]    [Pg.614]    [Pg.199]    [Pg.69]    [Pg.509]    [Pg.161]    [Pg.71]    [Pg.645]    [Pg.98]    [Pg.22]    [Pg.347]    [Pg.283]    [Pg.115]    [Pg.352]    [Pg.408]    [Pg.79]    [Pg.1]    [Pg.712]    [Pg.243]    [Pg.301]    [Pg.301]    [Pg.228]    [Pg.410]   


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