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Hydrochloric acid ionization

Gertner, B. J., and J. T. Hynes, Molecular Dynamics Simulation of Hydrochloric Acid Ionization at the Surface of Stratospheric Ice, Science, 271, 1563-1566 (1996). [Pg.714]

A solution containing 1 mol of hydrochloric acid ionizes as represented by the following equation. [Pg.462]

A double end point, acid—base titration can be used to determine both sodium hydrosulfide and sodium sulfide content. Standardized hydrochloric acid is the titrant thymolphthalein and bromophenol blue are the indicators. Other bases having ionization constants in the ranges of the indicators used interfere with the analysis. Sodium thiosulfate and sodium thiocarbonate interfere quantitatively with the accuracy of the results. Detailed procedures to analyze sodium sulfide, sodium hydro sulfide, and sodium tetrasulfide are available (1). [Pg.211]

Epichlorhydrin (ECH) detection starts with detecting epoxide cycle using hydrochloric acid in combination with sodium chloride the reaction product - 1,3-dichlorhydrin - is extracted in diethyl ether and concentrated by removing the latter. Gas-liquid chromatography with a flame-ionization detector is used to detect glycerin 1,3-dichlorhydrin. The sensitivity of the method is 0.01 mg/dm. ... [Pg.389]

A few binary molecular compounds containing H atoms ionize in water to form H+ ions. These are called acids. One such compound is hydrogen chloride, HC1 in water solution it exists as aqueous H+ and Cl- ions. The water solution of hydrogen chloride is given a special name It is referred to as hydrochloric acid. A similar situation applies with HBr and HI ... [Pg.42]

Szabo S, Nagy F. 1978. Investigations of bismuth adsorption via the ionization of hydrogen adsorbed on platinized platinum in hydrochloric acid solutions. J Electroanal Chem 87 261-265. [Pg.244]

Macerated plant material is homogenized with a mixture of methanol and 1.2N hydrochloric acid (HCl) in water (4 1, v/v) and then with methanol. An internal standard solution is added to the filtrate and the filtrate is adjusted to a constant volume. A portion of the filtrate is rotary evaporated to dryness and hexane is added to the extract before a Florisil cleanup procedure is performed. The extract is dissolved in toluene for analysis by GC/MS in the negative chemical ionization (NCI) mode. [Pg.1283]

The authors studied, as they call it, "acid-base equilibria in glacial acetic acid however, as they worked at various ratios of indicator-base concentration to HX or B concentration, we are in fact concerned with titration data. In this connection one should realize also that in solvents with low e the apparent strength of a Bronsted acid varies with the reference base used, and vice versa. Nevertheless, in HOAc the ionization constant predominates to such an extent that overall the picture of ionization vs. dissociation remains similar irrespective of the choice of reference see the data for I and B (Py) already given, and also those for HX, which the authors obtained at 25° C with I = p-naphthol-benzein (PNB) and /f B < 0.0042, i.e., for hydrochloric acid K C1 = 1.3 102, jjrfflci 3 9. IQ-6 an jjHC1 2.8 10 9 and for p-toluenesulphonic acid Kfm° = 3 7.102( K ms 4 0.10-6) Kmt = 7 3.10-9... [Pg.279]

Arrhenius proposed the idea that when an acid dissolves in water, it dissociates, or breaks, into its ions. This process is called ionization or disassociation. For example, the compound hydrogen chloride dissociates into a positive hydrogen ion and a negative chlorine ion when dissolved in water. This disassociation forms hydrochloric acid. [Pg.16]

Ans. One can add sodium acetate and hydrochloric acid. The reverse of the ionization reaction occurs, yielding acetic acid ... [Pg.313]

The addition of a cation to an olefin to produce a carbonium ion or ion pair need not end there but may go through many cycles of olefin addition before the chain is eventually terminated by neutralization of the end carbonium ion. Simple addition to the double bond is essentially the same reaction stopped at the end of the first cycle. The addition of mineral acids to produce alkyl halides or sulfates, for example, may be prolonged into a polymerization reaction. However, simple addition or dimerization is the usual result with olefins and hydrogen acids. The polymerization which occurs with a-methyl-styrene and sulfuric acid or styrene and hydrochloric acid at low temperatures in polar solvents is exceptional.291 Polymerization may also be initiated by a carbonium ion formed by the dissociation of an alkyl halide as in the reaction of octyl vinyl ether with trityl chloride in ionizing solvents.292... [Pg.152]

The ions that conduct the electrical current can result from a couple of sources. They may result from the dissociation of an ionically bonded substance (a salt). If sodium chloride (NaCl) is dissolved in water, it dissociates into the sodium cation (Na+) and the chloride anion (CL). But certain covalently bonded substances may also produce ions if dissolved in water, a process called ionization. For example, acids, both inorganic and organic, will produce ions when dissolved in water. Some acids, such as hydrochloric acid (HC1), will essentially completely ionize. Others, such as acetic acid (CH3COOH), will only partially ionize. They establish an equilibrium with the ions and the unionized species (see Chapter 13 for more on chemical equilibrium). [Pg.183]

Mercuric acetate It is essentially added to prevent the interference of the hydrochloric acid displaced through the formation of the relatively un-ionized HgCl2, thereby making a predominant shift in the equilibrium so that the titrimetric reaction is quantitative. [Pg.112]

It is therefore apparent that dissociation constants may only be compared in the same solvent. Ammonia is a stronger donor than water, but liquid ammonia has a much lower dielectric constant than the latter. The acidity constant of hydrochloric acid in liquid ammonia is much lower than in water, in which it is completely ionized and completely dissociated, whereas the complete ionization in liquid ammonia is not followed by extensive ionic dissociation due to its low dielectric constant. On the other hand, the acidity constant of acetic acid is somewhat higher in liquid ammonia than in water since in the latter if Ion is much lower than in liquid ammonia, in which complete ionization is achieved. [Pg.81]

Hydrochloric acid is a colorless to yellowish liquid (the yellow coloration may be due to traces of iron, chlorine or organics contaminants) fumes in air refractive index of 1.0 N solution 1.3417 density of commercial concentrated acid (37.8 g/lOOg solution) 1.19 g/mL, and constant boiling solution (20.22 g/lOOg solution) 1.096 g/mL at 25°C forms a constant boiling azeotrope with water at HCl concentration 20.22% the azeotrope boils at 108.6°C several metal chlorides can be salted out of their aqueous solutions by addition of HCl the addition of CaCL can break the azeotrope the pH of the acid at 1.0, 0.1 and 0.01 N concentrations are 0.10, 1.1, and 2.02, respectively a 10.0 M solution ionizes to 92.6% at 18°C. [Pg.358]

Bipyridine is likewise reduced to 4,4 -bipiperidine by sodium and amyl alcohol and by catalytic hydrogenation. " 2,2 -Dimethyl-4,4 -bipyridine is reduced to 2,2 -dimethyl-4,4 -bipiperidine. Electrochemical reduction of 4,4 -bipyridine affords 4,4 -bipiperidine and some partly reduced 4,4 -bipyridines. Further work on the electroreduction of 4,4 -bipyridine has been reported. Reduction of 4,4 -bipyridine by tin and hydrochloric acid " or by controlled catalytic hydrogenation - gives l,2,3,4,5,6-hexahydro-4,4 -bipyridine. 4,4 -Bipyridine is reduced to its 1,4-dihydro derivative by bisdihydropyridyl metal complexes and to its radical anion by alkali metals and related processes. " " The ionization constant of the radical anion has been determined. ... [Pg.332]

Table XII.—Molecular Conductivities and Degree of Ionization of Hydrochloric Acid at Different Temperatures. Table XII.—Molecular Conductivities and Degree of Ionization of Hydrochloric Acid at Different Temperatures.

See other pages where Hydrochloric acid ionization is mentioned: [Pg.14]    [Pg.826]    [Pg.11]    [Pg.48]    [Pg.14]    [Pg.826]    [Pg.11]    [Pg.48]    [Pg.71]    [Pg.515]    [Pg.271]    [Pg.482]    [Pg.58]    [Pg.611]    [Pg.622]    [Pg.60]    [Pg.105]    [Pg.149]    [Pg.157]    [Pg.187]    [Pg.521]    [Pg.333]    [Pg.303]    [Pg.393]    [Pg.98]    [Pg.352]    [Pg.267]    [Pg.161]    [Pg.262]    [Pg.603]    [Pg.93]    [Pg.132]    [Pg.191]    [Pg.195]    [Pg.234]   
See also in sourсe #XX -- [ Pg.182 ]

See also in sourсe #XX -- [ Pg.182 ]




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Acid ionization

Acids hydrochloric acid

Hydrochloric

Hydrochloric acid

Ionization of hydrochloric acid

Ionized acids

Reactions hydrochloric acid ionization

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