Ion weak acid

The Br0nsted theory expands the definition of acids and bases to allow us to explain much more of solution chemistry. For example, the Brpnsted theory allows us to explain why a solution of ammonium chloride tests acidic and a solution of sodium acetate tests basic. Most of the substances that we consider acids in the Arrhenius theory are also acids in the Bronsted theory, and the same is true of bases. In both theories, strong acids are those that react completely with water to form ions. Weak acids ionize only slightly. We can now explain this partial ionization as an equilibrium reaction of the ions, the weak acid, and the water. A similar statement can be made about weak bases ... 

Strategy Recall that strong acids and strong bases are strong electrolytes. They are completely ionized in solution. An ionic equation will show strong acids and strong bases in terms of their free ions. Weak acids and weak bases are weak electrolytes. They only ionize to a small extent in solution. Weak acids and weak bases are shown as molecules in ionic and net ionic equations. A net ionic equation shows only the species that actually take part in the reaction. 

CH3COOH] = 1.0 M, (negligible ions, weak acid) 0 unit... 

Weak adds are molecular compounds that have a weak tendency for producing H ions weak acids are incompletely ionized in aqueous solution. The vast majority of acids are weak acids. The ionization of a weak acid is best described in terms of a reversible reaction that does not go to completion. As described on page 156, the ionization reaction for acetic acid, CH3COOH, may be represented as... 

K2 is called the hydrolysis constant for sodium ethanoate. Hydrolysis occurs when salts involving weak acids or bases are dissolved in water. It is often also found with metal ions in solution. The ion [M(H20) ] dissociates to the hydroxy species [M(H20) , (OH)]f 1. ... 

Thus, ihe strongly basic oxide ion attacks the weakly acidic SiOj in a molten salt as solvent (p. 187 ... 

Pure hydrazoic acid is a colourless liquid, b.p. 310 K. It is very ready to detonate violently when subjected to even slight shock, and so is used in aqueous solution. It is a weak acid, reacting with alkali to give azides, which contain the ion Nj. 

The bond dissociation energy of the hydrogen-fluorine bond in HF is so great that the above equilibrium lies to the left and hydrogen fluoride is a weak acid in dilute aqueous solution. In more concentrated solution, however, a second equilibrium reaction becomes important with the fluoride ion forming the complex ion HFJ. The relevant equilibria are ... 

Chloric(III) acid is a fairly weak acid, and is an oxidising agent, for example it oxidises aqueous iodide ion to iodine. Sodium chlorate(III) (prepared as above) is used commercially as a mild bleaching agent it bleaches many natural and synthetic fibres without degrading them, and will also bleach, for example, oils, varnishes and beeswax. 

Writing the equation in the usual way directs too much attention to the atoms and not enough to the electrons We can remedy that by deleting any spec tator ions and by showing the unshared electron pairs and covalent bonds that are made and broken Both sodium hydroxide and sodium fluoride are com pletely ionized in water therefore Na" which ap pears on both sides of the equation is a spectator ion Hydrogen fluoride is a weak acid and exists as undissociated HF molecules in water... 

Example The pK s for the first and second ionizations of sulfuric acid are —48 and 2 0 respectively Sulfuric acid (HOSO2OH) is a strong acid hydrogen sulfate ion (H0S020 ) is a weak acid... 

Example A common misconception is that the conjugate base of a weak acid is strong This is sometimes but not always true It is true for example for ammo nia which is a very weak acid (pK 36) Its conjugate base amide ion (H2N ) is a much stronger base than HO It is not true however for acetic acid both acetic acid and its conjugate base acetate ion are weak The conjugate base of a weak acid will be strong only when the acid is a weaker acid than water... 

Although acetylene and terminal alkynes are far stronger acids than other hydro carbons we must remember that they are nevertheless very weak acids—much weaker than water and alcohols for example Hydroxide ion is too weak a base to convert acety lene to its anion m meaningful amounts The position of the equilibrium described by the following equation lies overwhelmingly to the left... 

Carbonic acid is formed when carbon dioxide reacts with water Hydration of car bon dioxide is far from complete however Almost all the carbon dioxide that is dis solved m water exists as carbon dioxide only 0 3% of it is converted to carbonic acid Carbonic acid is a weak acid and ionizes to a small extent to bicarbonate ion... 

Citing amine basicity according to the of the conjugate acid permits acid-base reac tions involving amines to be analyzed according to the usual Brpnsted relationships For example we see that amines are converted to ammonium ions by acids even as weak as acetic acid... 

Weak acid (Section 1 16) An acid that is weaker than 1130" Weak base (Section 1 16) A base that is weaker than HO Williamson ether synthesis (Section 16 6) Method for the preparation of ethers involving an Sfj2 reaction between an alkoxide ion and a primary alkyl halide... 

Carboxylate exchangers contain —COOH groups which have weak acidic properties and will only function as cation exchangers when the pH is sufficiently high (pH > 6) to permit complete dissociation of the —COOH site. Outside this range the ion exchanger can be used only at the cost of reduced capacity. 

Note that the concentration of H2O is omitted from the expression because its value is so large that it is unaffected by the dissociation reaction.The magnitude of provides information about the relative strength of a weak acid, with a smaller corresponding to a weaker acid. The ammonium ion, for example, with a Ka of 5.70 X 10 °, is a weaker acid than acetic acid. 

Positive-Tone Photoresists based on Dissolution Inhibition by Diazonaphthoquinones. The intrinsic limitations of bis-azide—cycHzed mbber resist systems led the semiconductor industry to shift to a class of imaging materials based on diazonaphthoquinone (DNQ) photosensitizers. Both the chemistry and the imaging mechanism of these resists (Fig. 10) differ in fundamental ways from those described thus far (23). The DNQ acts as a dissolution inhibitor for the matrix resin, a low molecular weight condensation product of formaldehyde and cresol isomers known as novolac (24). The phenoHc stmcture renders the novolac polymer weakly acidic, and readily soluble in aqueous alkaline solutions. In admixture with an appropriate DNQ the polymer s dissolution rate is sharply decreased. Photolysis causes the DNQ to undergo a multistep reaction sequence, ultimately forming a base-soluble carboxyHc acid which does not inhibit film dissolution. Immersion of a pattemwise-exposed film of the resist in an aqueous solution of hydroxide ion leads to rapid dissolution of the exposed areas and only very slow dissolution of unexposed regions. In contrast with crosslinking resists, the film solubiHty is controUed by chemical and polarity differences rather than molecular size. 

Because of the small size of the fluoride ion, F participates in coordination stmctures of high rank. Tantalum and niobium form stable hexafluorotantalate and hexafluoroniobate ions and hydrogen fluoride attacks these usually acid-resistant metals. Hydrogen fluoride in water is a weak acid. Two dissociation constants are... 

Because they are weak acids or bases, the iadicators may affect the pH of the sample, especially ia the case of a poorly buffered solution. Variations in the ionic strength or solvent composition, or both, also can produce large uncertainties in pH measurements, presumably caused by changes in the equihbria of the indicator species. Specific chemical reactions also may occur between solutes in the sample and the indicator species to produce appreciable pH errors. Examples of such interferences include binding of the indicator forms by proteins and colloidal substances and direct reaction with sample components, eg, oxidising agents and heavy-metal ions. 

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