Conjugate base, definition Conjugated

The Brensted-Lowry acid-base definition does not require that bases contain OH or that acid-base reactions occur in aqueous solution. It defines an acid as a species that donates a proton and a base as one that accepts It. An acid and a base act together in proton transfer. When an acid donates a proton, it becomes the conjugate base when a base accepts a proton, it becomes the conjugate acid. In an acid-base reaction, acids and bases form their conjugates. A stronger acid has a weaker conjugate base, and vice versa. Thus, the reaction proceeds in the net direction in which a stronger acid and base form a weaker base and acid. 

In the Bronsted-Lowry acid-base definition, a base is any species that accepts a proton therefore, there are many more Bronsted-Lowry bases than Arrhenius bases. When base B accepts a proton from acid HA, the species BH and A" form. HA and A" are a conjugate acid-base pair, as are BH and B. Thus, an acid-base reaction is a proton-transfer process between two conjugate acid-base pairs, with the stronger acid and base forming the weaker base and acid. (Section 18.3)... 

Br0nsted-Lowry acid-base definition (588) proton donor (588) proton acceptor (588) conjugate acid-base pair (589) Section 18.4... 

Buffers are solutions that tend to resist changes in their pH as acid or base is added. Typically, a buffer system is composed of a weak acid and its conjugate base. A solution of a weak acid that has a pH nearly equal to its by definition contains an amount of the conjugate base nearly equivalent to the weak acid. Note that in this region, the titration curve is relatively flat (Figure 2.15). Addition of H then has little effect because it is absorbed by the following reaction ... 

The products of proton transfer in aqueous solution may also react with water. For example, the CIST ion produced when HCN loses a proton to water can accept a proton from a water molecule and form HCN again. Therefore, according to the Bronsted definition, CN is a base it is called the conjugate base of the acid HCN. In general, a conjugate base of an acid is the species left when the acid donates a proton ... 

By definition, every carbanion possesses an unshared pair of electrons and is therefore a base. When a carbanion accepts a proton, it is converted to its conjugate acid (see Chapter 8). The stability of the carbanion is directly related to the strength of the conjugate acid. The weaker the acid, the greater the base strength and the lower the stability of the carbanion. Here, by stability we mean stability toward a proton donor the lower the stability, the more willing the carbanion is to accept a... 

There is little information for fluoro-substituted sulfinyl groups. Values of a and ffp for SOCFj based on benzoic acid ionization are 0.63 and 0.69 respectively , compared with values of about 0.52 and 0.49 for SOMe (Table 3). Thus the electronegative fluorine somewhat enhances the electron-attracting influence of the sulfinyl function and makes the order more definitely sulfur lone pair to engage in 7t(pp) conjugation. Values of and ffp for SOCF3 based on anilinium ion dissociation are 0.76 and 1.05 respectively . An increase of 0.13 as between and [Pg.509]

Regression analyses revealed systematic differences between experimental log P and log P calculations based on the summation of fragment values. These differences could be attributed to chemical characteristics of the molecules, which in turn allowed the definition of correction rules such as chain conjugation, electronegativity facing bulk or the proximity effect, which describes the presence of electronegative centers in a molecule separated by one or two carbons. Correction values needed for log P calculation were shown to represent multiples of a constant value of 0.289, which is known as the magic constant (CM). 

The chlorine ion can now accept a proton (and become hydrochloric acid again). If the chlorine can accept a proton, according to the Bronsted-Lowry definition, it is a base. Chemists actually call this chlorine ion the conjugate base of hydrochloric acid. Any time an acid gives up its proton, the substance that is left over can act as a base. So every acid has a conjugate base. 

The p/<, of a base is actually that of its conjugate acid. As the numeric value of the dissociation constant increases (i.e., pKa decreases), the acid strength increases. Conversely, as the acid dissociation constant of a base (that of its conjugate acid) increases, the strength of the base decreases. For a more accurate definition of dissociation constants, each concentration term must be replaced by thermodynamic activity. In dilute solutions, concentration of each species is taken to be equal to activity. Activity-based dissociation constants are true equilibrium constants and depend only on temperature. Dissociation constants measured by spectroscopy are concentration dissociation constants." Most piCa values in the pharmaceutical literature are measured by ignoring activity effects and therefore are actually concentration dissociation constants or apparent dissociation constants. It is customary to report dissociation constant values at 25°C. 

By definition, an acid will donate a proton to a base, and it is converted into its conjugate base. Conversely, a base will accept a proton from a... 

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