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With zinc

Prepared by treating 1,3-dibromopropane with zinc. It is a powerful gaseous anaesthetic, non-irritant and non-toxic to the liver and kidneys, but it is a respiratory depressant. [Pg.123]

CH2CI2. A colourless liquid with a chloroform-like odour b.p. 4I°C. Prepared by heating chloroform with zinc, alcohol and hydrochloric acid manufactured by the direct chlorination of methane. Decomposed by water at 200°C to give methanoic and hydrochloric acids. Largely used as a solvent for polar and non-polar substances, particularly for paint removal (30%), dissolving cellulose acetate and degreasing (10%). It is more stable than carbon tetrachloride or chloroform especially towards moisture or alkali. It is somewhat toxic. U.S. production 1981 280000 tonnes. [Pg.135]

It is prepared commercially by treating benzene diazonium chloride with sodium sulphite and then reducing the mixture with zinc dust and ethanoic acid. It can also be prepared by reduction of benzene diazonium chloride with SnCl. ... [Pg.305]

Treatment with PCI5 gives phthalyl chloride reduction with zinc and ethanoic acid or NaOH gives phthalide. Fusion with urea gives phthalimide. [Pg.312]

Gases which are high in FIjS are subject to a de-sulphurisation process in which H2S is converted into elemental sulphur or a metal sulphide. There are a number of processes based on absorption in contactors, adsorption (to a surface) in molecular sieves or chemical reaction (e.g. with zinc oxide). [Pg.254]

For example,copper has relatively good corrosion resistance under non-oxidizing conditions. It can be alloyed with zinc to yield a stronger material (brass), but with lowered corrosion resistance. Flowever, by alloying copper with a passivating metal such as nickel, both mechanical and corrosion properties are improved. Another important alloy is steel, which is an alloy between iron (>50%) and other alloying elements such as carbon. [Pg.923]

If a solid sulphite is heated with zinc dust (or carbon) the sulphite is reduced to sulphide ... [Pg.292]

It catalyses the decomposition of potassium chlorate(V). Mixed with zinc oxide, it is used as a catalyst in the manufacture of methanol. It is used as a pigment, being very resistant to weathering. [Pg.381]

Because of its resistance to corrosion, zinc may be used to coat iron. This may be done by dipping the iron into molten zinc or by spraying zinc on the iron articles, for example iron sheets. This is known as galvanising. Smaller iron articles may be coated by heating with zinc dust, a process known as sherardising, or suspensions of zinc may be used in paints. [Pg.418]

Cadmium is usually found in zinc ores and is extracted from them along with zinc (p. 416) it may be separated from the zinc by distillation (cadmium is more volatile than zinc. Table 14.2) or by electrolytic deposition. [Pg.434]

The Reformatsky Reaction consists of the interaction of an ester of an a-halogeno-acid with an aldehyde, a ketone or another ester in the presence of zinc. For example, if a mixture of ethyl bromoacetate and benzaldehyde is heated with zinc, the latter undoubtedly first combines with the ethyl bromoacetate to form a Grignard-like reagent (reaction A), which then adds on to the benzaldehyde Just as a Grignard reagent would do (reaction B). The complex so formed, on acidification gives ethyl p-phenyl-p-hydroxy-propionate (reaction C). Note that reaction A could not satisfactorily be carried out using... [Pg.286]

The Fischer Indolisation Reaction occurs when the phenylhydrazone of a suitable aldehyde or ketone undergoes cyclisation with loss of ammonia, under the influence of various reagents, such as zinc chloride, ethnnolic hydrogen chloride, or acetic acid. For example, the phenylhydrazone of acetophenone (p. 257) when heated with zinc chloride gives 2 phenylindole. ... [Pg.294]

Further reduction in alkaline solution (say, with zinc powder) leads to azobenzene and hydrazobenzene ... [Pg.628]

Reduction of nitrobenzene in methyl or ethyl alcoholic sodium hydroxide solution with zinc powder leads to azobenzene or hydrazobenzene according to the proportion of zinc powder employed ... [Pg.629]

Experimental details are given for o-phenylenedlamlne, which is conveniently prepared by the reduction of o-nitroaniline in alcoholic sodium hydroxide solution with zinc powder ... [Pg.640]

Reduction of ketones, with zinc powder and alcoholic sodium hydroxide leads to secondary alcohols, for example ... [Pg.811]

One method of preparing sulphlnic acids has already been described (diazo reaction. Section IV,65). Reduction of a sulphonyl chloride with zinc powder and water affords the zinc salt of the sulphinic acid, converted by sodium carbonate to the sodium salt (in which form it is conveniently isolated), and by hydrochloric acid into the somewhat unstable sulphinic acid, for example ... [Pg.821]

Thiophenols (or aryl mercaptans) are obtained by more vigorous reduction of sulphonyl chlorides (or of sulphinic acids), for example with zinc and dilute sulphuric acid, and are isolated by steam distillation ... [Pg.821]

When pyridine is treated with zinc dust and acetic anhydride, a type of reductive coupling occurs and the product is diacetyltetrahydrodipyridyl (I) this undergoes a curious change on heating yielding pyridine and a new diacetyl compound, 1 4 diacetyl 1 4-dihydropyridine (II). The latter is reduced by zinc and acetic acid to 4-ethylpyridine (III). [Pg.844]

Reactor-grade zirconium is essentially free of hafnium. Zircaloy(R) is an important alloy developed specifically for nuclear applications. Zirconium is exceptionally resistant to corrosion by many common acids and alkalis, by sea water, and by other agents. Alloyed with zinc, zirconium becomes magnetic at temperatures below 35oK. [Pg.56]

Indium is most frequently associated with zinc materials, and it is from these that most commercial indium is now obtained however, it is also found in iron, lead, and copper ores. [Pg.116]

Jote 2. We have also carried out this synthesis in ethanol as a solvent but the results were not reproducible. Although a series of experiments with zinc powder from one flask gave reasonable results (50-78% yields), a new flask with the same batch number gave low yields of impure products. The main impurity was probably the non-conjugated diene, H2C=CH-CH2-CH=CH-CH3, possibly resulting from reduction of the 1,2,4-triene by the zinc. The... [Pg.192]

C—C double bonds may be protected against electrophiles by epoxidation and subsequent removal of the oxygen atom by treatment with zinc and sodium iodide in acetic acid (J.A. Edwards, 1972 W. Kndll, 1975). Halogenation has often been used for protection, too. The C—C double bond is here also easily regenerated with zinc (see p. 138, D.H.R. Barton, 1976). [Pg.156]

Trichloro- and 2,2,2-tribromoethoxycarbonyl (Tceoc and Tbeoc) protecting groups are introduced with the commercially available 2,2,2-trihaloethyl chloroformates. These derivatives are stable towards CrOj and acids, but can smoothly be cleaved by reduction with zinc in acetic acid at 20 °C to yield 1,1-dihaloethene and CO. Several examples in lipid (F.R. Pfeiffer, 1968, 1970) and nucleotide syntheses (A.F. Cook, 1968) have been described. [Pg.158]


See other pages where With zinc is mentioned: [Pg.74]    [Pg.169]    [Pg.294]    [Pg.306]    [Pg.312]    [Pg.314]    [Pg.315]    [Pg.375]    [Pg.386]    [Pg.433]    [Pg.383]    [Pg.142]    [Pg.451]    [Pg.571]    [Pg.748]    [Pg.748]    [Pg.748]    [Pg.69]    [Pg.114]    [Pg.245]    [Pg.44]    [Pg.109]    [Pg.268]    [Pg.326]    [Pg.335]   
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Acids zinc with hydrochloric acid

Addition Reactions with Copper-Zinc Reagents

Alloys with zinc

Allylic chlorides, reaction with zinc-copper

Association with zinc

BINOL zinc complexes with

Binding Motifs with Zinc Ions

Bronze compared with zinc

CS Modified with Zinc, Titanium, and Zirconium Oxides

Cadmium interactions with zinc

Cathodic protection with zinc paints

Chelation with zinc borohydride

Chloro ketones reduction with zinc

Chlorophosphines, reaction with zinc

Cobalt, alloy with zinc

Complexes with zinc compounds

Copper compared with zinc

Copper ions reactions with zinc metal

DNA complex with zinc finger protein

Dehalogenation, with zinc

Di-2-pyridylamine with zinc

Dialkyl zincs, alkylations with

Diastereoselectivity, with zinc borohydride

Diethyl zinc, reaction with carbenes

Dimethyl zinc, reaction with

Dimethyl zinc, reaction with cobalt

Dimethyl zinc, reaction with cobalt complexes

Dimethylformamide with zinc

Dispersant with zinc

Dissolving metal reductions with zinc

Electroplating with zinc

Eliminations with zinc

Enones reaction with zinc ester enolates

Esters with zinc permanganate

Grignard reagent zinc halide reaction with

Humidity with zinc carbonate

Hydrochloric acid reaction with zinc

Hydrochloric acid reaction with zinc sulfide

Hydrochloric acid with zinc

Hydrochloric acid zinc reacting with

Hydrogen chloride zinc reaction with dissolved form

Hydrogen chloride, reaction with zinc

Insulin association with zinc

Iodine reaction with zinc

Iodoethane, reaction with zinc

Iodomethane reaction with zinc

Ketones, reaction with zinc borohydride

Light with zinc carbonate

Lithium salt of 2- -l,2thiaborolide, reaction with ruthenium and zinc complexes

Lithium, zinc oxide doped with

Mercury amalgamation with zinc

Neutralization with zinc acetate

Nitric acid reaction with zinc

Nitro-ketones, reduction with zinc

Operation with Zinc Oxide

Organometallic compounds with zinc

Oxygen reaction with zinc sulfide

Phenols distillation with zinc

Preparation with zinc/copper couple

Propionic acid, a-bromoethyl ester reaction with zinc

Propylene with zinc oxide

Reaction with zinc metal

Reactions with Aryl Zinc Compounds

Reactions with zinc ester dieneolates

Reactions with zinc ester dienolates

Reactions with zinc oxide

Reduction of an a,-Unsaturated y-Diketone with Zinc

Reduction with amalgamated zinc the Jones reductor

Reduction with zinc powder

Reduction with zinc/copper couple

Reduction, by amalgamated zinc and with simultaneous amination

Reductions with Zinc

Reductive decarboxylation with zinc-copper

Reductive elimination with zinc copper couple

Silver® ions, reaction with zinc

Spraying with zinc

Spraying with zinc mixed metal coatings

Spraying with zinc sealing

Substitution Reactions with Copper-Zinc Reagents

Substitution reactions asymmetric, with zinc compounds

Substitution reactions with zinc compounds

Sulfonyl chlorides reduction with zinc

Sulfur reaction with zinc

Sulfur removal with zinc oxide

Sulfur zinc with

Synthesis applications with zinc reagents

Thiocarbamates with zinc

Three-dimensional structures with zinc finger protein

Vinyl halides cross-coupling with zincs

Vitamin interaction with zinc

Zinc , redox with complexes

Zinc Amalgam reduction with

Zinc Oxide Ointment with Vitamin E and Aloe

Zinc Phosphates with Extra-large Pores and Chiral Open Frameworks

Zinc alkyls reactions with

Zinc aryls reactions with

Zinc borohydride reduction with

Zinc catalysis addition with

Zinc cation, interactions with coordinating

Zinc chloride compound with

Zinc chloride compound with hydrocyanic acid

Zinc chloride, acetonation catalyst with

Zinc chloride, acetonation catalyst with acetic acid

Zinc chloride, reaction with phenylmagnesium bromide

Zinc compared with nickel

Zinc complex, with octaethylporphyrin

Zinc complexes with

Zinc coordination, functionalized with amides

Zinc cyanide reaction with aromatic compounds

Zinc determination with the graphite-tube technique (Furnace method)

Zinc diethyl-: Simmons-Smith reaction with

Zinc doped with aluminium

Zinc ester enolates reaction with conjugated enones

Zinc halides reactions with

Zinc halides, allylreactions with silylated alkynes

Zinc hydrides reactions with

Zinc interface with oxygen

Zinc oxide reaction with, phosgene

Zinc oxide reactions with propylene

Zinc porphyrin, complex with

Zinc powder distillation with

Zinc reaction with hydrochloric

Zinc reagents cross-coupling with alkyl halides

Zinc reagents with aryls

Zinc reagents with n-bound ligands

Zinc with EDTA

Zinc with permanganate

Zinc, 2-pentenylbromoreaction with diisobutyl ketone

Zinc, alkynylchlororeaction with alkenyl halides

Zinc, alkynylchlororeaction with alkenyl halides palladium-catalyzed

Zinc, allylbromoreaction with aldoxime ethers

Zinc, allylbromoreaction with aldoxime ethers dependence of product ratio on solvent

Zinc, allylchlororeaction with aldehydes

Zinc, allylreaction with aldehydes

Zinc, arylchlorocoupling reactions with alkenyl bromides

Zinc, bis hydride donor reaction with phenyl isopropyl ketone

Zinc, bis reaction with benzaldehyde

Zinc, bromo reaction with alkynes

Zinc, chloro-2-furylcoupling reactions with alkenyl iodides

Zinc, cinnamylreactions with aldehydes

Zinc, crotylreaction with aldehydes

Zinc, crotylreaction with aldehydes regioselectivity

Zinc, crotylreaction with aldehydes syn-anti selectivity

Zinc, diallylreactions with a-alkoxyaldehydes

Zinc, diallylreactions with a-alkoxyaldehydes stereoselectivity

Zinc, diallylreactions with oximes

Zinc, diallylreactions with oximes diastereoselective

Zinc, dibutylreaction with benzaldehyde

Zinc, dicrotylreactions with aldehydes

Zinc, dicrotylreactions with aldehydes stereoselectivity

Zinc, diethylSubject reaction with 1,2-diketones

Zinc, diethylSubject reaction with benzaldehyde

Zinc, homoallylcoupling reactions with aromatic halides

Zinc, homopropargylcoupling reactions with aromatic halides

Zinc, organo- reagents reactions with

Zinc, propargylreactions with aldimines

Zinc, propargylreactions with aldimines Knoevenagel reaction

Zinc, propargylreactions with aldimines catalyst

Zinc, reaction with alkyl halides

Zinc-copper reagents reactions with acid chlorides

Zincs reactions with

Zinc—carbon bonds reactions with

Zinc—copper reactions with

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