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Acids metals reacting with

Lead azide tends to hydrolyze at high humidities or in the presence of materials evolving moisture. The hydrazoic acid formed reacts with copper and its alloys to produce the sensitive cupric azide [14215-30-6] Cu(N2)2- Appropriate protection must be provided by hermetic sealing and the use of noncopper or coated-copper metal. [Pg.10]

The mote electropositive metals react with cryohte, Hberating aluminum or aluminum monofluotide (22,23). The reduction of cryohte by magnesium is a current method for removal of magnesium in the refining of aluminum. Upon contact with strong acids cryohte Hberates hydrogen fluoride. [Pg.143]

The most important appHcation of metal alkoxides in reactions of the Friedel-Crafts type is that of aluminum phenoxide as a catalyst in phenol alkylation (205). Phenol is sufficientiy acidic to react with aluminum with the formation of (CgH O)2Al. Aluminum phenoxide, when dissolved in phenol, greatiy increases the acidic strength. It is beheved that, similar to alkoxoacids (206) an aluminum phenoxoacid is formed, which is a strong conjugate acid of the type HAl(OCgH )4. This acid is then the catalyticaHy active species (see Alkoxides, metal). [Pg.564]

Metals. Most metals react with aqueous HCl foUowing equation 22. The reaction rate is dependent on the concentration of the acid, oxidi2ing, reducing, or complexing agents, and corrosion inhibitors, in addition to the metallurgical characteristics of the material and the prevailing hydrodynamic conditions (see Corrosion and corrosion control). [Pg.446]

Reactions of the Hydroxyl Group. The hydroxyl proton of hydroxybenzaldehydes is acidic and reacts with alkahes to form salts. The lithium, sodium, potassium, and copper salts of sahcylaldehyde exist as chelates. The cobalt salt is the most simple oxygen-carrying synthetic chelate compound (33). The stabiUty constants of numerous sahcylaldehyde—metal ion coordination compounds have been measured (34). Both sahcylaldehyde and 4-hydroxybenzaldehyde are readily converted to the corresponding anisaldehyde by reaction with a methyl hahde, methyl sulfate (35—37), or methyl carbonate (38). The reaction shown produces -anisaldehyde [123-11-5] in 93.3% yield. Other ethers can also be made by the use of the appropriate reagent. [Pg.505]

Manganese metal reacts with many compounds (21). Although Mn is fairly stable against water at room temperature, a slow reaction accompanied by the evolution of hydrogen takes place at 100°C. Most dilute acids dissolve manganese at a fast rate. At 350—875°C, anhydrous ammonia converts Mn... [Pg.503]

Aromatic amines form addition compounds and complexes with many inorganic substances, such as ziac chloride, copper chloride, uranium tetrachloride, or boron trifluoride. Various metals react with the amino group to form metal anilides and hydrochloric, sulfuric, or phosphoric acid salts of aniline are important intermediates in the dye industry. [Pg.229]

Pyrrole is soluble in alcohol, benzene, and diethyl ether, but is only sparingly soluble in water and in aqueous alkaUes. It dissolves with decomposition in dilute acids. Pyrroles with substituents in the -position are usually less soluble in polar solvents than the corresponding a-substituted pyrroles. Pyrroles that have no substituent on nitrogen readily lose a proton to form the resonance-stabilized pyrrolyl anion, and alkaU metals react with it in hquid ammonia to form salts. However, pyrrole pK = ca 17.5) is a weaker acid than methanol (11). The acidity of the pyrrole hydrogen is gready increased by electron-withdrawing groups, eg, the pK of 2,5-dinitropyrrole [32602-96-3] is 3.6 (12,13). [Pg.354]

Whereas the addition of early metal soaps to a coating for the specific purpose of improving the drying performance did so, the compounds lacked uniformity of composition and therefore did not give predictable results. Even if all of the metal reacted with the acid to give an expected metal ion concentration, which seldom happened, the ions were subject to oxidation, which resulted in loss of solubiUty in the vehicle and therefore a loss of activity. [Pg.217]

Oxidation of SO2 is slow in a mixture of pure gases, but the rate is increased by light, NO2, oxidants, and metallic oxides which act as catalysts for the reaction. The formed acids can react with particulate matter or ammonia to form salts. [Pg.31]

Chemical Reactivity - Reactivity with Water Reacts violently and may cause flashes of fire. Hydrochloric acid fumes are fonned in the reaction Reactivity with Common Materials Corrodes most common constmction materials. Reacts with water to form hydrochloric acid, which reacts with most metals to form flammable hydrogen gas Stability During Transport Stable Neutralizing Agents for Acids and Caustics Flush with water neutralize acids formed with lime or soda ash Polymerization Not pertinent Inhibitor of Polymerization Not pertinent. [Pg.317]

The metals react with most non-metals especially if heated, but resist alkali attack and are less reactive towards acids than might be expected. Concentrated HCl probably reacts most rapidly, but even here insoluble residues remain in the cases of Th (black). Pa (white) and U (black). Those of Th and U have the approximate compositions HThO(OH) and UH(OH)2. Concentrated HNO3 passivates Th, U and Pu, but the addition of F ions avoids this and provides the best general method for dissolving these metals. [Pg.1264]

Acetylenes are sufficiently acidic to react with sodium metal to generate acetylides, useful nucleophiles in the formation of carbon-carbon bonds. The reaction is classically carried out in liquid ammonia, which is a good solvent for alkali metals but which is troublesome to handle. Two convenient modifications of the acetylide generation reaction overcome this difficulty and are discussed below along with the classical method. [Pg.121]

Thus for the equilibrium attained when zinc metal reacts with acid,... [Pg.331]

Not all metals react with aqueous acids. Among the common metals, magnesium, aluminum, iron, and nickel liberate H2 as zinc does. Other metals, including copper, mercury, silver, and gold, do not produce measurable amounts of hydrogen even though we make sure that the equilibrium state has been attained. With these metals, hydrogen is not produced and it is surely not just because of slow reactions. Apparently... [Pg.203]

Aluminum metal reacts with aqueous acidic solutions to liberate hydrogen gas. Write the two half-reactions and the net ionic reaction. [Pg.222]

Many heavy metals react with dithiol to give coloured precipitates, e.g. bismuth, iron(III), copper, nickel, cobalt, silver, mercury, lead, cadmium, arsenic, etc. molybdate and tungstate also react. Of the various interfering elements, only arsenic distils over with the tin when a mixture is distilled from a medium of concentrated sulphuric acid and concentrated hydrobromic acid in a current of carbon dioxide. If arsenic is present in quantities larger than that of the tin it should be removed. [Pg.695]

PET is the polyester of terephthalic acid and ethylene glycol. Polyesters are prepared by either direct esterification or transesterification reactions. In the direct esterification process, terephthalic acid is reacted with ethylene glycol to produce PET and water as a by-product. Transesterification involves the reaction of dimethyl terephthalate (DMT) with ethylene glycol in the presence of a catalyst (usually a metal carboxylate) to form bis(hydroxyethyl)terephthalate (BHET) and methyl alcohol as a by-product. In the second step of transesterification, BHET... [Pg.527]

Magnesium metal reacts with aqueous acid solution to generate hydrogen gas. The expanded views are molecular pictures of each phase. [Pg.63]

C04-0105. Iron metal reacts with hydrochloric acid to give H2 gas and Fe ions. If 5.8 g of iron is to be... [Pg.269]

Magnesium, a Group 2 metal, reacts with acids to generate +2 cations ... [Pg.323]

Metals do not dissolve in water, because they contain extensive delocalized bonding networks that must be disrupted before the metal can dissolve. A few metals react with water, and several reacf with aqueous acids, but no metal will simply dissolve in water. Likewise, metals do not dissolve in nonpolar liquid solvents. [Pg.841]

C17-0028. Sodium metal reacts with ammonia to form an ionic salt, NaNH2, that contains NH2 anions. Is this salt acidic or basic, and why What reaction occurs if this salt is placed in water ... [Pg.1251]

Boron trihalides are strong Lewis acids that react with a wide collection of Lewis bases. Many adducts form with donor atoms from Group 15 (N, P, As) or Group 16 (O, S). Metal fluorides transfer F ion to BF3 to give tetrafluoroborate salts LiF + BF3 LiBF4 Tetrafluoroborate anion is an important derivative of BF3 because it is nonreactive. With four <7 bonds, [BF4 ] anion has no tendency to coordinate further ligands. Tetrafluoroborate salts are used in synthesis when a bulky inert anion is necessary. [Pg.1522]

Although it has been known since 19051 that very pure chromium metal reacts with acids, under oxygen-free conditions, to produce large quantities of chromium (II), this approach to the preparation of chromium(II) compounds has not been developed. Rather, syntheses generally involved (1) reduction of chro-mium(III), either by electrolytic means or by chemical agents (for example Zn/Hg), or (2) metathetical procedures. Both methods are inefficient and often lead to impure products. Recently2-8 extensive use of reactions between electrolytic chromium and various acids has led to the synthesis of a wide variety of chromium (II) complexes which would be considerably more difficult to prepare by other methods.9-11... [Pg.31]

Although aliphatic alcohols are not normally acidic, the OH group is sufficiently acidic to react with very active metals such as sodium. The reaction can be written as... [Pg.300]

Reactions of selected metal complexes of multidentate amines with formaldehyde and a range of carbon acids (such as nitroethane) have led to ring-closure reactions to yield a series of three-dimensional cage molecules (see Chapter 3). Condensations of this type may also be used to produce two-dimensional macrocycles (Comba et al., 1986) - see [2.20], In such cases, it appears that imine intermediates are initially produced by condensation of the amines with formaldehyde as in the Curtis reaction. This is followed by attack of the conjugate base of the carbon acid on an imine carbon. The resulting bound (new) carbon acid then reacts with a second imine in a cis site to yield chelate ring formation. [Pg.40]

The standard reduction potential for Be2+ is the least negative of the elements in the group and by the same token beryllium is the least electropositive and has the greatest tendency to form covalent bonds. The bulk metal is relatively inert at room temperature and is not attacked by air or water at high temperatures. Beryllium powder is somewhat more reactive. The metal is passivated by cold concentrated nitric acid but dissolves in both dilute acid and alkaline solutions with the evolution of dihydrogen. The metal reacts with halogens at 600°C to form the corresponding dihalides. [Pg.115]

Hydrogen sulfide is a weak acid that reacts with most heavy metals and produces a corresponding metal sulfide with a low solubility in water. With a divalent metal, the total reaction is as follows ... [Pg.148]


See other pages where Acids metals reacting with is mentioned: [Pg.74]    [Pg.98]    [Pg.164]    [Pg.386]    [Pg.445]    [Pg.516]    [Pg.505]    [Pg.28]    [Pg.47]    [Pg.23]    [Pg.156]    [Pg.258]    [Pg.486]    [Pg.566]    [Pg.1417]    [Pg.30]    [Pg.42]    [Pg.107]    [Pg.458]    [Pg.471]    [Pg.575]    [Pg.240]   


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