Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Acidity and conjugate base

Product acids and bases such as those formed in this process are termed conjugate acids and conjugate bases. Thus, all acid-base reactions can be written as... [Pg.85]

Use curved arrows to track electron movement and identify the acid base con jugate acid and conjugate base... [Pg.35]

Hydrogen was recognized as the essential element in acids by H. Davy after his work on the hydrohalic acids, and theories of acids and bases have played an important role ever since. The electrolytic dissociation theory of S. A. Arrhenius and W. Ostwald in the 1880s, the introduction of the pH scale for hydrogen-ion concentrations by S. P. L. Sprensen in 1909, the theory of acid-base titrations and indicators, and J. N. Brdnsted s fruitful concept of acids and conjugate bases as proton donors and acceptors (1923) are other land marks (see p. 48). The di.scovery of ortho- and para-hydrogen in 1924, closely followed by the discovery of heavy hydrogen (deuterium) and... [Pg.32]

The concentration of the acid is usually of the order 0.05-0.2 mol L" Similar remarks apply to weak bases. It is clear that the greater the concentrations of acid and conjugate base in a buffer solution, the greater will be the buffer capacity. A quantitative measure of buffer capacity is given by the number of moles of strong base required to change the pH of 1 litre of the solution by 1 pH unit. [Pg.48]

Step 4 Find the concentrations of acid and conjugate base from fj] = Hj/V, where the total volume is V = Vanalvte +... [Pg.581]

Aufbau principle See building-up principle. autoionization See autoprotolysis. autoprotolysis A reaction in which a proton is transferred between two molecules of the same substance. The products are the conjugate acid and conjugate base of the substance. Example ... [Pg.941]

C17-0119. Aqueous solutions of Na2 SO3 and CH3 CO2 H are mixed, (a) List the major species in each solution, (b) Write the net ionic reaction that occurs on mixing, (c) Identify the acid, base, conjugate acid, and conjugate base. [Pg.1269]

Buffer capacity is determined by the amounts of weak acid and conjugate base present in the solution. If enough H3 O is added to react completely with the conjugate base, the buffer is destroyed. Likewise, the buffer is destroyed if enough OH is added to consume all of the weak acid. Consequently, buffer capacity depends on the overall concentration as well as the volume of the buffer solution. A buffer solution whose overall concentration is 0.50 M has five times the capacity as an equal volume of a buffer solution whose overall concentration is 0.10 M. Two liters of 0.10 M buffer solution has twice the capacity as one liter of the same buffer solution. Example includes a calculation involving buffer capacity. [Pg.1284]

The Henderson-Hasselbach equation, Equation (6.50), relates the pH of a buffer solution to the amounts of conjugate acid and conjugate base it contains ... [Pg.270]

As base is added, a mixture of weak acid and conjugate base is formed. This is a buffer solution and can be treated as one in the calculations. Determine the moles of acid consumed from the moles of titrant added—that will be the moles of conjugate base formed. Then calculate the molar concentration of weak acid and conjugate base, taking into consideration the volume of titrant added. Finally, apply your buffer equations. [Pg.224]

Three experimental methods that are capable of determining dissociation constants with a precision of the order of tenths of 1% have been most commonly used. Each of these methods—the cell potential method (2), the conductance method (3), and the optical method (4)—provides data that can be treated approximately, assuming that the solutions obey Henry s law, or more exactly on the basis of the methods developed in Chapter 19. We will apply the more exact procedures. As the optical method can be used only if the acid and conjugate base show substantial differences in absorption of visible or ultraviolet light, or differences in raman scattering or with the use of indicators, we shall limit our discussion to the two electrical methods. [Pg.472]

The amino acids in question are the basic amino acids lysine, arginine, and histidine, and the acidic amino acids aspartic acid and glutamic acid. The side-chain functions of these amino acids, ionized at pH 7 (see Box 4.7), act as acids or bases. In a reverse sequence, protons may be acquired or donated to regenerate the conjugate acids and conjugate bases. [Pg.517]

The most effective acid-base catalyst is one whose pATa is 7.0, since at pH 7.0 the concentrations of acid and conjugate base are equal (see Section 4.9). With just a slight decrease in pH it would become... [Pg.517]

You re given a pH and a which suggests that you need to use the Henderson-Hasselbalch equation. You have the total concentration of acid and conjugate base, but you don t know either of the concentrations in the equation individually, so begin by solving for their ratio ... [Pg.246]

Equation 2.6 is the familiar Henderson-Hasselbalch equation, which defines the relationship between pH and the ratio of acid and conjugate base concentrations. The Henderson-Hasselbalch equation is of great value in buffer chemistry because it can be used to calculate the pH of a solution if the molar ratio of buffer ions ([A-]/[HA]) and the pKa of HA are known. Also, the molar ratio of HA to A- that is necessary to prepare a buffer solution at a specific pH can be calculated if the pKa is known. [Pg.40]

In addition to changing the pH of the water, the uptake and release of CO2 alter the buffer capacity of the water. The effect upon buffer capacity is the result of two factors (1) the dependence of buffer capacity on the hydrogen ion concentration, and (2) the dependence of buffer capacity on the total concentration of weak acid and conjugate base in solution (67, 68). The precipitation of CaCO in natural waters reduces the buffer capacity to a value lower than that predicted on the basis of pH change and respiratory or photosynthetic changes in COL content of the water. [Pg.335]

The pH of a buffer solution does not depend on the volume of the solution. Because a change in solution volume changes the concentrations of the acid and base by the same amount, the [base]/[acid] ratio and the pH remain unchanged. As a result, the volume of water used to prepare a buffer solution is not critical, and you can dilute a buffer without a change in pH. The pH depends only on pKa and on the relative molar amounts of weak acid and conjugate base. [Pg.676]

A solution of a weak acid and its conjugate base is called a buffer solution because it resists drastic changes in pH. The ability of a buffer solution to absorb small amounts of added H30+ or OH- without a significant change in pH (buffer capacity) increases with increasing amounts of weak acid and conjugate base. The pH of a buffer solution has a value close to the pKa (— log Ka) of the weak acid and can be calculated from the Henderson-Hasselbalch equation ... [Pg.708]

SOLUTION The acid-base equilibrium for this reaction is shown in the following figure. Determining the relative amounts of the acid and conjugate base requires direct substitutions in the Henderson-Hasselbalch equation (Equation 9.1). The pH is 7.0, and the pk-., is 4.2. The equation evaluates to reveal that the ratio of the conjugate base to the acid is 630 1. As a check on this result, since pH 7.0 is more basic than the pKa of benzoic acid, the conjugate base should predominate. [Pg.222]

COSMO models [27-30] were compared with the SM approach [22] by Klamt [43] and by Cramer and Truhlar [44]. A very recent paper by Klamt and coworkers [45] shows that improved calculated pKa values are obtained for the limited domain of strong to moderately weak acids by a cluster-continuum method in which the acid and conjugate base are each associated with one or a few solvent molecules and this cluster is then continuum-calculated with COSMO-RS. The authors point out, however, that for the calculation of pKa a consistent and generally applicable method is still lacking . This paper clarifies the problem raised in [41]. The matter is under study.1... [Pg.531]

Barker et al. (1961) found such a correlation for Malachite Green cations. It is not necessary, however, that the acid and conjugate base frequency shifts should separately be related to the substituent a-values in this way for a good correlation to be obtained between a and the difference in their frequency shifts, i.e. the difference in their frequency maxima and hence in p (Sj)—pAT(S0). Figure 10 shows a plot of Av against a for substituted 5-phenylazotropolones, the acid and base forms of which separately showed very erratic... [Pg.192]

Sample In the chemical reaction shown below, identify the Bronsted-Lowry acid, Bronsted-Lowry base, conjugate acid, and conjugate base ... [Pg.317]

Write an equation that shows the reaction between hypochlorous acid and water. Identify the acid, base, conjugate acid, and conjugate base in this reaction. [Pg.19]


See other pages where Acidity and conjugate base is mentioned: [Pg.50]    [Pg.270]    [Pg.14]    [Pg.229]    [Pg.434]    [Pg.225]    [Pg.257]    [Pg.369]    [Pg.667]    [Pg.128]    [Pg.131]    [Pg.140]    [Pg.154]    [Pg.674]    [Pg.124]    [Pg.152]    [Pg.72]    [Pg.187]    [Pg.189]   
See also in sourсe #XX -- [ Pg.53 ]

See also in sourсe #XX -- [ Pg.53 ]

See also in sourсe #XX -- [ Pg.53 ]




SEARCH



Bases conjugate

Bases conjugate base

Conjugate acid and

Conjugate acids and bases

© 2024 chempedia.info