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Acid-base, generally

Many solution reactions are catalyzed by hydrogen or hydroxyl ions and consequently may undergo accelerated decomposition upon the addition of acids or bases. The catalysis of a reaction by hydrogen or hydroxyl ions is known as acid-base specific catalysis. In many cases, in addition to the effect of pH on reaction rate, there may be catalysis by one or more species of the buffer system. This type of catalysis is known as the acid-base general catalysis. Solutions of vitamin were found to be... [Pg.351]

Chem. Descrip. Short oil aikyd resin in Rule 66 exempt solvent blend Uses Aikyd for lacquers, baking and air dry industrial coatings Features Tall oil fatty acid-based general purpose Properties Gardner 6 max. color dens. 8.12 Ib/gai vise. (Gardner-Hoidt) Z1-Z3 acid no. 5-10 60% NV Setal 11-1390 [Akzo Nobel Resins]... [Pg.732]

As an adjective applied to metals base represents the opposite of noble, i.e. a base metal would be attacked by mineral acids, base exchange An old term used to describe the capacity of soils, zeolites, clays, etc. to exchange their cations (Na, K, Ca ) for an equivalent of other cations without undergoing structural change. An example of the general process of ion exchange. ... [Pg.52]

When an amine, or a solution of its hydrochloride, is added to an aqueous solution of chloroplatinic acid, a salt of the base with the cliloroplatinic acid, of general formula BjiHiPtCle (where B is one molecule of the base) is formed and usually crystallises out, for these chloroplatinates hai e normally a rather low solubility in cold water. The chloroplatinate can be filtered off, dried, and then analysed by direct ignition, when only the metallic platinum ultimately remains. Knowing the percentage of platinum in the chloroplatinate, the molecular weight of the latter, and hence of the constituent base, can readily be calculated. [Pg.449]

The Lewis definitions of acids and bases provide for a more general view of acid-base reactions than either the Arrhenius or Br0nsted-Lowry pic ture A Lewis acid is an electron pair acceptor A Lewis base is an electron pair donor The Lewis approach incorporates the Br0nsted-Lowry approach as a subcategory m which the atom that accepts the electron pair m the Lewis acid is a proton... [Pg.50]

These relationships are general Hydroxyl substituted purines and pyrimidines exist in their keto forms ammo substituted ones retain structures with an ammo group on the ring The pyrimidine and punne bases m DNA and RNA listed m Table 28 1 follow this general rule Beginning m Section 28 7 we 11 see how critical it is that we know the cor rect tautomeric forms of the nucleic acid bases... [Pg.1157]

Although this treatment of buffers was based on acid-base chemistry, the idea of a buffer is general and can be extended to equilibria involving complexation or redox reactions. For example, the Nernst equation for a solution containing Fe + and Fe + is similar in form to the Henderson-Hasselbalch equation. [Pg.170]

The titration curve in Figure 9.1 is not unique to an acid-base titration. Any titration curve that follows the change in concentration of a species in the titration reaction (plotted logarithmically) as a function of the volume of titrant has the same general sigmoidal shape. Several additional examples are shown in Figure 9.2. [Pg.276]

Although many quantitative applications of acid-base titrimetry have been replaced by other analytical methods, there are several important applications that continue to be listed as standard methods. In this section we review the general application of acid-base titrimetry to the analysis of inorganic and organic compounds, with an emphasis on selected applications in environmental and clinical analysis. First, however, we discuss the selection and standardization of acidic and basic titrants. [Pg.298]

Sensitivity For an acid-base titration we can write the following general analytical equation... [Pg.312]

As with acid-base and complexation titrations, redox titrations are not frequently used in modern analytical laboratories. Nevertheless, several important applications continue to find favor in environmental, pharmaceutical, and industrial laboratories. In this section we review the general application of redox titrimetry. We begin, however, with a brief discussion of selecting and characterizing redox titrants, and methods for controlling the analyte s oxidation state. [Pg.341]

Determination of Equilibrium Constants Another important application of molecular absorption is the determination of equilibrium constants. Let s consider, as a simple example, an acid-base reaction of the general form... [Pg.407]

In developing this treatment for determining equilibrium constants, we have considered a relatively simple system in which the absorbance of HIn and Im were easily measured, and for which it is easy to determine the concentration of H3O+. In addition to acid-base reactions, the same approach can be applied to any reaction of the general form... [Pg.409]

The yield of acrylonitrile based on propylene is generally lower than the yield of acryhc acid based on the dkect oxidation of propylene. Hence, for the large volume manufacture of acrylates, the acrylonitrile route is not attractive since additional processing steps are involved and the ultimate yield of acrylate based on propylene is much lower. Hydrolysis of acrylonitrile can be controUed to provide acrylamide rather than acryhc acid, but acryhc acid is a by-product in such a process (80). [Pg.155]

Acid-Base Behavior. The relative acidity-basicity of the filler, generally determined by measuring the pH value of a slurry of a specific mass of filler in 100 mL of deionized water, can influence the behavior of a filler in some systems. For example, the curing behavior of some elastomers is sensitive to the pH value of carbon black. [Pg.367]

Ethylene glycol was originally commercially produced in the United States from ethylene chlorohydrin [107-07-3J, which was manufactured from ethylene and hypochlorous acid (eq. 8) (see Chlorohydrins). Chlorohydrin can be converted direcdy to ethylene glycol by hydrolysis with a base, generally caustic or caustic/bicarbonate mix (eq. 9). An alternative production method is converting chlorohydrin to ethylene oxide (eq. 10) with subsequent hydrolysis (eq. 11). [Pg.358]

The general manufacturing scheme for phosphate salts is shown in Figure 11. Condensed phosphates are prepared from the appropriate orthophosphate or mixture of orthophosphates, so the preparation of orthophosphates must be considered first for the manufacture of any phosphate salt. Phosphoric acid is neutralized to form a solution or slurry with a carefully adjusted acid/base ratio according to the desired orthophosphate product. The orthophosphate may be recovered either by crystallization from solution, or the entire solution or slurry may be evaporated to dryness. The dewatering (qv) method is determined by the solubihty properties of the product and by its desired physical properties such as crystal size and shape, bulk density, and surface area. Acid orthophosphate salts may be converted to condensed phosphates by thermal dehydration (calcination). [Pg.340]

Carboxyhc acid ester, carbamate, organophosphate, and urea hydrolysis are important acid/base-catalyzed reactions. Typically, pesticides that are susceptible to chemical hydrolysis are also susceptible to biological hydrolysis the products of chemical vs biological hydrolysis are generally identical (see eqs. 8, 11, 13, and 14). Consequentiy, the two types of reactions can only be distinguished based on sterile controls or kinetic studies. As a general rule, carboxyhc acid esters, carbamates, and organophosphates are more susceptible to alkaline hydrolysis (24), whereas sulfonylureas are more susceptible to acid hydrolysis (25). [Pg.218]

With pteridine (1) the covalent hydration is a complex matter since the general acid-base catalyzed reaction provides a good example of a kinetically controlled addition to the... [Pg.286]

Aromatic pyrazoles and indazoles, in the broad sense defined in Sections 4.04.1.1.1 and 4.04.1.1.2, will be discussed here. Tautomerism has already been discussed (Section 4.04.1.5) and acid-base equilibria will be considered in Section 4.04.2.1.3. These two topics are closely related (Scheme 10) as a common anion (156a) or a common cation (156b) is generally involved in the mechanism of proton transfer (e.g. 78T2259). For aromatic pyrazoles with exocyclic conjugation there is also a common anion (157) for the three tautomeric forms... [Pg.217]

The tilkalinity and acidity is generally controlled, based on the timounts itnd also by maintaining the pH vtilue of the effluent discharge between. 1.5. and 9,0. the ideal being tirotind 7.5. as far tis possible. The pH can be checked w ith the help of a pH meter. [Pg.417]

The formation of oximes, hydrazones, and related imine derivatives is usually catalyzed by both general acids and general bases. General base catalysis of dehydration of the tetrahedral intermediate involves nitrogen deprotonation concerted with elimination of hydroxide ion. ... [Pg.460]


See other pages where Acid-base, generally is mentioned: [Pg.448]    [Pg.98]    [Pg.448]    [Pg.98]    [Pg.242]    [Pg.1298]    [Pg.97]    [Pg.144]    [Pg.311]    [Pg.815]    [Pg.70]    [Pg.399]    [Pg.226]    [Pg.512]    [Pg.172]    [Pg.235]    [Pg.398]    [Pg.459]    [Pg.162]    [Pg.414]    [Pg.13]    [Pg.14]    [Pg.2423]    [Pg.344]    [Pg.14]    [Pg.20]    [Pg.192]    [Pg.4]    [Pg.38]   


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Acid-base theory generalized

Acid-base, generally equilibria, characteristics

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Catalysis, acid-base generalized

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Experimental studies of general acid—base catalysis

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General Acid-Base Catalysis in Model Systems

General Properties of Acids and Bases

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General acid base catalysis intramolecular

General acid-base catalysis mechanisms

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General acid-base catalysis, determination

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General base

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General concepts of acids and bases

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