Ammonium ions water

The previous calculation assumed that the solvation energy of ammonium was equal the solvation energy of a single water molecule times the number of water binding sites. Is this a valid assumption Compare the electrostatic potential maps of ammonium ion and ammonium ion+water. For which are the exposed hydrogens more acidic Did the calculation underestimate or overestimate the difference in solvation energies ... 

Figure 4.8 Tetrahedral recognition the soccer ball cryptand as a receptor for ammonium ion, water or chloride, depending on the pH of the medium.

In base the tetrahedral intermediate is formed m a manner analogous to that pro posed for ester saponification Steps 1 and 2 m Figure 20 8 show the formation of the tetrahedral intermediate m the basic hydrolysis of amides In step 3 the basic ammo group of the tetrahedral intermediate abstracts a proton from water and m step 4 the derived ammonium ion dissociates Conversion of the carboxylic acid to its corresponding carboxylate anion m step 5 completes the process and renders the overall reaction irreversible... 

In addition to hydrogen bonding between the two polynucleotide chains the double helical arrangement is stabilized by having its negatively charged phosphate groups on the outside where they are m contact with water and various cations Na" Mg and ammonium ions for example Attractive van der Waals forces between the... 

Anhydrous aluminum triduotide, A1F., is a white crystalline soHd. Physical properties are Hsted ia Table 2. Aluminum duotide is spatingly soluble ia water (0.4%) and iasoluble ia dilute mineral acids as well as organic acids at ambient temperatures, but when heated with concentrated sulfuric acid, HF is hberated, and with strong alkah solutions, aluminates are formed. A1F. is slowly attacked by fused alkahes with the formation of soluble metal duotides and aluminate. A series of double salts with the duotides of many metals and with ammonium ion can be made by precipitation or by soHd-state reactions. 

In addition to cost, several factors influence the choice of salt for a particular appHcation. The ammonium salt is the most soluble in water, but for some apphcations the presence of the ammonium ion maybe undesirable. The sodium salt is almost as soluble as the ammonium salt at ambient temperatures and above. The potassium salt is much less soluble. 

Addition of a salt can transform the shale by cation exchange to a less sensitive form of clay, or reduce the osmotic swelling effect by reducing the water activity in the mud below that which occurs in the shale. These effects depend on the salt concentration and the nature of the cation. Salts containing sodium, potassium, calcium, magnesium, and ammonium ions ate used to varying degrees. 

Complex Ion Formation. Phosphates form water-soluble complex ions with metallic cations, a phenomenon commonly called sequestration. In contrast to many complexing agents, polyphosphates are nonspecific and form soluble, charged complexes with virtually all metallic cations. Alkali metals are weakly complexed, but alkaline-earth and transition metals form more strongly associated complexes (eg, eq. 16). Quaternary ammonium ions are complexed Htde if at all because of their low charge density. The amount of metal ion that can be sequestered by polyphosphates generally increases... 

Aluminum Sulfate (Alum). Alum, a double sulfate of potassium and aluminum having twelve waters of crystallization, KA1(S0 2 12H20, is the earliest referenced aluminum containing compound. It was mentioned by Herodotus in the fifth century BC. The Egyptians used alum as a mordant and as a medicine the Romans used it for fireproofing. Some alums contain sodium or ammonium ions in place of potassium. 

Ammonia and ammonium ions in industrial water streams, including waste-water streams, can be determined by either of two methods (ASTM Procedure D1426). In the first, the sample is buffered to a pH of 7.4 and distilled into a solution of boric acid where the ammonia nitrogen is deterrnined colorimetricaHy with Nessler reagents or titrated using standard sulfuric acid. 

There are a considerable number of stable crystalline salts of the ammonium ion [14798-03-9] NH. Several are of commercial importance because of large scale consumption in fertiliser and industrial markets. The ammonium ion is about the same size as the potassium and mbidium ions, so these salts are often isomorphous and have similar solubiUty in water. Compounds in which the ammonium ion is combined with a large, uninegative anion are usually the most stable. Ammonium salts containing a small, highly charged anion generally dissociate easily into ammonia (qv) and the free acid (1). At about 300°C most simple ammonium salts volatilize with dissociation, for example... 

Of the cations (counterions) associated with polar groups, sodium and potassium impart water solubiUty, whereas calcium, barium, and magnesium promote oil solubiUty. Ammonium and substituted ammonium ions provide both water and oil solubiUty. Triethanolammonium is a commercially important example. Salts (anionic surfactants) of these ions ate often used in emulsification. Higher ionic strength of the medium depresses surfactant solubihty. To compensate for the loss of solubiUty, shorter hydrophobes ate used for appHcation in high ionic-strength media. The U.S. shipment of anionic surfactants in 1993 amounted to 49% of total surfactant production. 

The chromate(VI) salts containing the tetrahedral CrO ion are a very important class of Cr(VI) compounds. Only the alkah metal, ammonium ion, and magnesium chromates show considerable water-solubiHty. Some cations, eg,, and, are so insoluble that they precipitate from... 

In Table 11 data were given ou the proton transfer from the ammonium ion to a water molecule... 

Substituted Ammonium Ions. Like NH4C1 the substance NH3-(CH3JCI, where a CH3 group has been substituted for one hydrogen, forms a crystalline solid and so do the substances NH2(CH3)2C1 and NH(CH3)3C1. When one of these substances is dissolved in water, it is completely dissociated into Cl- ions and molecular positive ions corresponding to (NH4)+. Suppose now that such a solution contains an NH3 molecule, and consider the following proton transfer... 

These equations say that the Kh of an amine multiplied by the of the corresponding ammonium ion is equal to Kw, the ion-product constant for water (1.00 x 10 14). Thus, if we know Ka for an ammonium ion, we also know for the corresponding amine base because /stronger base has an ammonium ion with a larger p... 

It s often possible to lake advantage of their basicity to purify amines. For example, if a mixture of a basic amine and a neutral compound such as a ketone or alcohol is dissolved in an organic solvent and aqueous acid is added, the basic amine dissolves in the water layer as its protonated salt, while the neutral compound remains in the organic solvent layer. Separation of the water layer and neutralization of the ammonium ion by addition of NaOH then provides the pure amine (Figure 24.2). 

Notice that in each case the oxygen or nitrogen atom is surrounded by eight valence electrons. In each species, a single electron pair is shared between two bonded atoms. These bonds are called single bonds. There is one single bond in the OH- ion, two in the H20 molecule, three in NH3, and four in NH4+. There are three unshared pairs in the hydroxide ion, two in the water molecule, one in the ammonia molecule, and none in the ammonium ion. 

Cations. The ammonium ion, NH,+, behaves as a weak acid in water a 0.10 M solution of NH4CI has a pH of about 5. The process by which the NH4+ ion lowers the pH of water can be represented by the (Bransted-Lowry) equation ... 

Acidic ion Ion that forms H+ ions in water. The ammonium ion is acidic because of the reaction NHi+(flq) — ... 

Two types of compounds, crystalline and amorphous, can be precipitated from tantalum or niobium solutions by an initial ammonia solution containing ammonium ions, with an interface at about pH = 10. Such solutions are used for the stripping of tantalum or niobium from TBP extracts. In the case of pure fluorotantalic or fluoroniobic acids that result from the stripping process with water, the interface occurs at a lower pH level. 

The salt ammonium sulfate, (NH4>2S04, dissolves in water to form a conducting solution containing ammonium ions, NH, and sulfate ions,... 

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