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L- -chlorid

A 60 per cent, excess of chlorosulphonic acid is used a smaller excess loads to increased formation of diphenylsulphone (CgH SOjC Hg) at the expense of the Bulphonj l chloride. [Pg.822]

Diazotization of a primary arylamine followed by treatment of the diazo mum salt with copper(l) bromide or copper(l) chloride yields the corre spending aryl bromide or aryl chloride... [Pg.973]

Chloride. Chloride is common in freshwater because almost all chloride salts are very soluble in water. Its concentration is generally lO " to 10 M. Chloride can be titrated with mercuric nitrate. Diphenylcarbazone, which forms a purple complex with the excess mercuric ions at pH 2.3—2.8, is used as the indicator. The pH should be controlled to 0.1 pH unit. Bromide and iodide are the principal interferences, whereas chromate, ferric, and sulfite ions interfere at levels greater than 10 mg/L. Chloride can also be deterrnined by a colorimetric method based on the displacement of thiocyanate ion from mercuric thiocyanate by chloride ion. The Hberated SCN reacts with ferric ion to form the colored complex of ferric thiocyanate. The method is suitable for chloride concentrations from 10 to 10 M. [Pg.231]

Typical brines received at an Arkansas bromine plant have 3—5 g/L bromide, 200—250 g/L chloride, 0.15—0.20 g/L ammonia, 0.1—0.3 g/L hydrogen sulfide, 0.01—0.02 g/L iodide, and additionally may contain some dissolved organics, including natural gas and cmde oil. The bromide-containing brine is first treated to remove natural gas, cmde oil, and hydrogen sulfide prior to introduction into the contact tower (48). [Pg.285]

Polychloroprene rubber (CR) is the most popular and versatile of the elastomers used in adhesives. In the early 1920s, Dr. Nieuwland of the University of Notre Dame synthesized divinyl acetylene from acetylene using copper(l) chloride as catalyst. A few years later, Du Pont scientists joined Dr. Nieuwland s research and prepared monovinyl acetylene, from which, by controlled reaction with hydrochloric acid, the chloroprene monomer (2-chloro-l, 3-butadiene) was obtained. Upon polymerization of chloroprene a rubber-like polymer was obtained. In 1932 it was commercialized under the tradename DuPrene which was changed to Neoprene by DuPont de Nemours in 1936. [Pg.589]

Suspension polymerization produces beads of plastic for styrene, methyl methacrviaie. viny l chloride, and vinyl acetate production. The monomer, in which the catalyst must be soluble, is maintained in droplet fonn suspended in water by agitation in the presence of a stabilizer such as gelatin each droplet of monomer undergoes bulk polymerization. In emulsion polymerization, ihe monomer is dispersed in water by means of a surfactant to form tiny particles held in suspension I micellcsK The monomer enters the hydrocarbon part of the micelles for polymerization by a... [Pg.277]

For the in situ preparation of the required arenediazonium salt from an aryl amine by application of the diazotization reaction, an acid HX is used, that corresponds to the halo substituent X to be introduced onto the aromatic ring. Otherwise—e.g. when using HCl/CuBr—a mixture of aryl chloride and aryl bromide will be obtained. The copper-(l) salt 2 (chloride or bromide) is usually prepared by dissolving the appropriate sodium halide in an aqueous solution of copper-(ll) sulfate and then adding sodium hydrogensulfite to reduce copper-(ll) to copper-(1). Copper-(l) cyanide CuCN can be obtained by treatment of copper-(l) chloride with sodium cyanide. [Pg.248]

Common salt, or sodium chloride, is also present in dissolved form in drilling fluids. Levels up to 3,000 mg/L chloride and sometimes higher are naturally present in freshwater muds as a consequence of the salinity of subterranean brines in drilled formations. Seawater is the natural source of water for offshore drilling muds. Saturated brine drilling fluids become a necessity when drilling with water-based muds through salt zones to get to oil and gas reservoirs below the salt. [Pg.682]

Azomethane. CA Registry No 503-28-6. The following supplements the article in Vol 1, A655-R under Azomethane Preparation. It has been prepd by the oxidn of N,N -dimethylhydrazine with K dichromate (Ref 2). The action of Cu(II) sulfate in aq Na acetate contg HC1, Na chloride, or Cu(II) chloride on the same hydrazine gives the Cu(l) chloride complex of azomethane (Refs 3 13)... [Pg.84]

Rhodium-catalysed addition (10) of hydridosilanes (Chapter 17) to a/3-unsaturated carbonyl compounds can be performed regioselectively, to afford either the product of 1,2-addition, or, perhaps more usefully, that of 1,4-addition, i.e. the corresponding silyl enol ether this latter process is an excellent method for the regiospecific generation of silyl enol ethers. Of all catalyst systems investigated, tris(triphenylphosphine)rhodium(l) chloride proved to be the best. [Pg.146]

Terephthaloyl Chloride-Isophthaloy l Chloride-Bisphenol-A Interfacial Polyesterification... [Pg.110]

FIGURE 11.22 When ammonia is added to a silver chloride precipitate, the precipitate dissolves. However, when ammonia is added to a precipitate of mercury(l) chloride, mercury metal and mercury(ll) ions are formed in a redox reaction and the mass turns gray. Left to right silver chloride in water, silver chloride in aqueous ammonia, mercury(l) chloride in water, and mercury(l) chloride in aqueous ammonia. [Pg.596]

Using the equilibrium constants below, calculate the concentrations of free (uncomplexed) cadmium ion in a freshwater with a chloride concentration of 15 mg/L, and in seawater containing 17 000 mg/L chloride. Ignore com-plexation with other ions. [Pg.415]

Thionyl chloride. This reagent (b.p. 76°) is generally used in excess of the theoretical quantity it cannot be employed for acet5 l chloride (b.p. 52°) because of the diflBculty of separation by fractional distillation. Excellent results are obtained, however, with butyric acid and acids of higher molecular weight, for example ... [Pg.367]

TO, a 77-year-old male nursing home resident is admitted to the hospital with a 3-day history of altered mental status. The patient was unable to give a history or review of systems. On physical examination the vital signs revealed a blood pressure of 100/60 mm Hg, pulse 110 beats per minute, respirations 14/minutes, and a temperature of 101°F (38.3°C). Rales and dullness to percussion were noted at the posterior right base. The cardiac exam was significant for tachycardia. No edema was present. Laboratory studies included sodium 160 mEq/L (160 mmol/L), potassium 4.6 mEq/L (4.6 mmol/L), chloride 120 mEq/L (120 mmol/L), bicarbonate 30 mEq/L (30 mmol/L), glucose 104 mg/dL (5.77 mmol/L), BUN 34 mg/dL (12.14 mmol/L), and creatinine 2.2 mg/dL (194.5 pmol/L). The CBC was within normal limits. Chest x-ray indicated a right lower lobe pneumonia. [Pg.416]

The injection zone contains about 7900 mg/L chloride, but less than 32 km (20 miles) northeast of the injection site, chloride concentrations are less than 250 mg/L. Under natural conditions, water... [Pg.838]

CL/L Chloride content per unit weight of lignin (mmole/g)... [Pg.203]

Table 4.1. Most commona ML compounds (L = chloride, oxide, alkyl) and number of unpaired electrons1 (eu) for group 3-12 transition metals M asterisks... Table 4.1. Most commona ML compounds (L = chloride, oxide, alkyl) and number of unpaired electrons1 (eu) for group 3-12 transition metals M asterisks...
Based on their interest in medium-size ring synthesis, Takahashi and co-workers used a copper(l) salt to mediate the [4+ 4]-reaction of zirconacyclopentadienes 82a, 82b and 82d and l,2-bis(bromomethyl)arenes (Scheme 31).85 The reaction works with substoichiometric amounts of copper(l) chloride (10 mol%), but in general higher yields and faster reaction times are observed with 2 equiv. [Pg.620]


See other pages where L- -chlorid is mentioned: [Pg.198]    [Pg.439]    [Pg.436]    [Pg.218]    [Pg.343]    [Pg.961]    [Pg.406]    [Pg.161]    [Pg.961]    [Pg.441]    [Pg.600]    [Pg.974]    [Pg.373]    [Pg.2359]    [Pg.88]    [Pg.288]    [Pg.313]    [Pg.332]    [Pg.374]    [Pg.383]    [Pg.387]    [Pg.394]    [Pg.406]    [Pg.408]    [Pg.691]    [Pg.1268]    [Pg.345]    [Pg.425]    [Pg.511]    [Pg.152]   


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1.1- Dimethyl-l- hydrazonium chloride

2-Chloro-l-methylpyridinium chloride

2-Ethoxy-l-naphthoyl chloride

2-Oxo-2,3-dihydropyrido -l,4benzoxazinium chloride

2.4.6- Trichloro-l,3,5-triazine cyanuric chloride)

4- Phenyl-l,2,3,5-dithiadiazolium chloride

4-Ethyl-2,3-dioxo-l-piperazinocarbonyl chloride

4.5- Dichloro-l,2,3-dithiazolium chloride

Adamantane-l-carboxylic acid chloride

Aluminum chloride/l-methyl-3-ethylimidazolium

D,l-10-Camphorsulfonyl chloride

Dehydrochlorination, of acid chlorides from l- -4-chloro-2butene

Dichlorobis(l,2-ethanediamine)cobalt(III) Chloride

Dichlorobis(l,2-ethanediamine)platinum(IV) Chloride

L chloride

L chloride

L-Allyl-3-methylimidazolium chloride

L-Dodecyl-3-methylimidazolium chloride

L-Hexadecyl-3-methylimidazolium chloride

L-Octyl-3-methylimidazolium chloride

L-Threonyl chloride, 2-acetyl-3,4-isopropylidene

L-butyl-3-methyl imidazolium chloride

L-butyl-3-methylimidazolium chloride

L-butyl-3-methylimidazolium chloride bmimCl)

L-ethyl-3-methyl imidazolium chloride

L-ethyl-3-methylimidazolium chloride

L-methyl-3-octylimidazolium chloride

L’oseo-rhodium salts chloride

Sulfoxides, alk-l-enyl phenyl with thionyl chloride

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