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Acid-base reactions titration

A titration in which the reaction between the analyte and titrant is an acid—base reaction. [Pg.278]

The experimental setup for a titration is shown in Figure 4.7. The flask contains vinegar, a water solution of a weak organic add called acetic acid. A solution of sodium hydroxide of known concentration is added from a buret. The net ionic equation for the acid-base reaction that occurs is... [Pg.84]

The discussion of acid-base titrations in Chapter 4 focused on stoichiometry. Here, the emphasis is on the equilibrium principles that apply to the acid-base reactions involved. It is convenient to distinguish between titrations involving—... [Pg.394]

As described in Chapter 4, acid-base reactions that go to completion can be exploited in chemical analysis using the method of titration. Titrations can be understood in greater detail from the perspective of acid-base equilibria. Protonation of a weak base by a strong acid is a reaction that goes virtually to completion because of its large... [Pg.1290]

During the titration with the nitrogen base B (which as a titrant must be a stronger base than the solvent Py), there are the competitive acid-base reaction ... [Pg.282]

In an early work by Mertz and Pettitt, an open system was devised, in which an extended variable, representing the extent of protonation, was used to couple the system to a chemical potential reservoir [67], This method was demonstrated in the simulation of the acid-base reaction of acetic acid with water [67], Recently, PHMD methods based on continuous protonation states have been developed, in which a set of continuous titration coordinates, A, bound between 0 and 1, is propagated simultaneously with the conformational degrees of freedom in explicit or continuum solvent MD simulations. In the acidostat method developed by Borjesson and Hiinenberger for explicit solvent simulations [13], A. is relaxed towards the equilibrium value via a first-order coupling scheme in analogy to Berendsen s thermostat [10]. However, the theoretical basis for the equilibrium condition used in the derivation seems unclear [3], A test using the pKa calculation for several small amines did not yield HH titration behavior [13],... [Pg.270]

In a titration, the equivalence point is the point at which chemically equivalent amounts of reactants have reacted, whereas the end point is the point at which an indicator changes color and a titration should be stopped. So, a chemist needs to be careful when choosing an indicator in an acid-base reaction, to be certain that the pH at which the indicator changes color is close to the pH at the equivalence point of the titration. [Pg.335]

The chromophore in hydrangeas is delphinidin (X), which is a member of the anthrocyanidin class of compounds. Compound X reminds us of phenol (VII), indicating that delphinidin is also a weak acid. In fact, all pH indicators are weak acids or weak bases, and the ability to change colour is a visible manifestation of the indicator s ability to undergo reversible changes in structure. In the laboratory, only a tiny amount of the pH indicator is added to the titration solution, so it is really just a probe of the solution pH. It does not participate in the acid-base reaction, except insofar as its own structure changes with the solution pH. [Pg.274]

A common laboratory application of acid-base reactions is titration. A titration is a laboratory procedure in which we use a solution of known concentration to determine some information (such as concentration and mass) about an unknown substance. A titration may involve any type of reaction—acid-base, redox, and so on. In this section, we will only consider acid-base titrations. The... [Pg.70]

In this chapter, we investigate individual types of reactions that meet all the requirements. We will also discuss back titrations, in which some of the limitations that we may encounter are solved. Our discussions in Chapter 4 involved acid-base reactions. These reactions as well as other applicable reactions will also be discussed here. [Pg.99]

In general, titrations governed by precipitation reactions do not really constitute an appreciable number in volumetric determinations in comparison to either redox or acid-base reactions. The interaction between silver-nitrate and sodium chloride in solutions result into the precipitation of silver chloride as shown below ... [Pg.151]

For an indicator to be useful in detecting the end-point of an acid-base reaction, the pH range of the indicator must fit into the vertical part of the titration curve for that reaction. The vertical part of the titration curve will include the pH of the salt solution at the end-point. [Pg.105]

Perrone et al. (2001) modelled Ni(II) adsorp-tion to synthetic carbonate fluoroapatite (CaI0 ((P04)5(C03))(0H,F). The solid phase had a pHIEP of 6.3 and a ZPC of 6.4 with an SSA of 8.8m2/g, an estimated sorption site density of 3.1 sites/nm2. They conducted 8-day isotherms in closed vessels at Ni concentrations of 5 x 10-10 to 1 x 10 8 M, constant I (0.05, 0.1 or 0.5 M), constant solid phase concentrations of 10 g/dm3 at pH values of 4 to 12. As Ni sorption occurred, no significant release of Ca was seen. Sorption was reversible. Rather than precisely characterize surface functional groups, they elected to describe their sorbent surfaces using acid-base reactions for the average behaviour of all sites involved in protonation and deprotonation. Potentiametric titration data were used to estimate the constants with the FTTEQL computer code ... [Pg.444]

As we have covered, titration is used to determine the concentration of an unknown substance in acid-base reactions through the use of a known concentration in a solution. It can also be used in oxidation-reduction reactions for the same analytical... [Pg.159]

Acid-base reactions in non-aqueous solvents have been extensively studied. Many books and reviews are available concerning acid-base equilibria and acid-base titrations in non-aqueous solvents. References [1-3] are particularly useful. [Pg.61]

Titration of a 0.7865 g sample of pure potassium hydrogen phthalate requires 35.73 ml of a NaOH solution. Calculate the molarity of the NaOH solution. This acid-base reaction is... [Pg.196]

The neutralisation of acids with bases provides many valuable volumetric methods of chemical analysis and redox titrations are useful as well. But here we encounter an important difference between acid/base and redox reactions in solution. Acid/base reactions which involve the transfer of protons are very fast indeed they are usually instantaneous for all practical purposes. In protonic solvents, polar H-X bonds are very labile and undergo rapid proton exchange. For example, if B(OH)3 - a very weak acid - is recrystallised from D20, we obtain a fully-deuterated product. Redox reactions, on the other hand, are often very slow under ordinary conditions. To return to the analogy between acid/base and redox titrations, many readers will be familiar with the reaction between permanganate and oxalic acid the reaction is very slow at room temperature and, for titrimetric purposes, should be carried out at about 60 °C. The mechanism whereby a redox reaction takes place tends to be... [Pg.333]

Alkalinity is a measure of the acid-neutralising capacity of water and is usually determined by titration against sulphuric acid to the endpoint of the acid—base reaction. In groundwaters, the carbonate species predominate and an endpoint of... [Pg.43]

Acid-base reactions are of particular interest because one can titrate the NMR sample and observe a titration curve of chemical shifts. This is because the two forms (protonated and unprotonated) usually show chemical shift differences at one or more sites near the... [Pg.423]

Simulation Results. A onc-dimensional simulation model based on the Nernst-Planck and Poisson equations [14, in which all the acid-base reactions occurring in the membrane are taken into account, has been used to give a qualitative description of the pH step titration process. In these simulations, a pH step is applied outside a 2 mm thick stagnant layer, which is assumed to be present in front of an 8 mm thick membrane. Diffusion coefficients in the membrane are assumed to be 4/10 of those in water (this value is based on experience with ion step experiments). Lysozyme, used as a model protein, is assumed to contain 11 carboxylic groups (pKa = 4.4), 2 imidazole groups (pKa = 6.0), and 9 amino groups (pKa = 10.4) per molecule. Concern... [Pg.380]

Acid-base reactions are of particular analytical interest [10]. Titration of filmed silica with sodium hydroxide seems not to be a very exciting reaction. But the advantage of a acid-base reaction is that it distinguishes easily between the acidic silanols of silica and any other kind of monomeric, polymeric or resinous silanols. Titration may be a helpful tool to follow the degree of reaction of silica silanol groups with a variety of silylating agents. [Pg.767]

Under suitable reaction conditions the acid-base reaction provides a hydroxyl capacity or silanol group density of fumed silica of about 2 SiOH per nm. This veilue falls well between the total amount of silanol groups on fumed silica of about 2.5 SiOH per nm [11] and 1.7 SiOH per nm as reported for the content of reactive isolated silanol groups [12]. Titration seems to give a good estimation about the content of chemically reactive and available silanol groups. [Pg.768]

The analytical chemistry of redox reactions in nonaqueous solvents has received less attention than acid-base reactions in these solvents. It should be a fruitful subject for future study. Thus far the Karl Fischer titration for water has been the most... [Pg.293]

The enthalpy change of some reactions can be measured directly, but for those that do not go to completion (as is common in acid-base reactions), thermodynamic data from reactions that do go to completion can be combined using Hess s law to obtain the needed data. For example, the enthalpy and entropy of ionization of a weak acid, HA, can be found by measming (1) the enthalpy of reaction of HA with NaOH, (2) the enthalpy of reaction of a strong acid (such as HCl) with NaOH, and (3) the equilibrium constant for dissociation of the acid (usually determined from the titration curve). [Pg.193]


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