Alkanes chloride

Silicon, unlike carbon, does notiorm a very large number of hydrides. A series of covalently bonded volatile hydrides called silanes analogous to the alkane hydrocarbons is known, with the general formula Si H2 + 2- I uf less than ten members of the series have so far been prepared. Mono- and disilanes are more readily prepared by the reaction of the corresponding silicon chloride with lithium aluminium hydride in ether ... 

Direct Borohydride Reduction of Alcohols to Alkanes with Phosphonium Anhydride Activation N-Proovlbenzene. To a solution of 5.56 g (20 mmol) of triphenylphosphine oxide in 30mL of dry methylene chloride at CfC was added dropwise a solution of 1.57 mL (10 mmol) of triflic anhydride in 30mL of dry methylene chloride. After 15 min when the precipitate appeared, a solution of 1.36g (10 mmol) of 3-phenyl-1-propanol in 10 mL of dry methylene chloride was added and the precipitate vanished in 5 min. An amount of 1.5g (40 mmol) of sodium borohydride was added as a solid all at once and the slurry was stirred at room temperature for... 

Ethylene oxide Acids and bases, alcohols, air, 1,3-nitroaniline, aluminum chloride, aluminum oxide, ammonia, copper, iron chlorides and oxides, magnesium perchlorate, mercaptans, potassium, tin chlorides, alkane thiols... 

ALKYLATION OF ALIPHATIC COMPOUNDS The first reported alkylation of branched-chain alkanes by ethylene, over aluminum chloride (69), made it possible to alkylate alkanes (except methane and ethane) with straight chain or branched alkenes. 

Reaction conditions depend on the reactants and usually involve acid or base catalysis. Examples of X include sulfate, acid sulfate, alkane- or arenesulfonate, chloride, bromide, hydroxyl, alkoxide, perchlorate, etc. RX can also be an alkyl orthoformate or alkyl carboxylate. The reaction of cycHc alkylating agents, eg, epoxides and a2iridines, with sodium or potassium salts of alkyl hydroperoxides also promotes formation of dialkyl peroxides (44,66). Olefinic alkylating agents include acycHc and cycHc olefinic hydrocarbons, vinyl and isopropenyl ethers, enamines, A[-vinylamides, vinyl sulfonates, divinyl sulfone, and a, P-unsaturated compounds, eg, methyl acrylate, mesityl oxide, acrylamide, and acrylonitrile (44,66). 

Simultaneous treatment of an alkane with sulfur dioxide and chlorine affords a sulfonyl chloride, eg, hexylsulfonyl chloride [14532-24-2] and is referred to as chlorosulfonation or the Reed reaction (247,248). 

Poly(vinyl nitrate) has been prepared and studied for use in explosives and rocket fuel (104,105). Poly(vinyl alcohol) and sulfur trioxide react to produce poly(vinyl sulfate) (106—111). Poly(vinyl alkane sulfonate)s have been prepared from poly(vinyl alcohol) and alkanesulfonyl chlorides (112—114). In the presence of urea, poly(vinyl alcohol) and phosphoms pentoxide (115) or phosphoric acid (116,117) yield poly(vinyl phosphate)s. 

Chemical Properties. Like neopentanoic acid, neodecanoic acid, C2QH2QO2, undergoes reactions typical of carboxyHc acids. For example, neodecanoic acid is used to prepare acid chlorides, amides (76), and esters (7,11,77,78), and, like neopentanoic acid, is reduced to give alcohols and alkanes (21,24). One area of reaction chemistry that is different from the acids is the preparation of metal salts. Both neopentanoic acid and neodecanoic acid, like all carboxyHc acids, can form metal salts. However, in commercial appHcations, metal salt formation is much more important for neodecanoic acid than it is for neopentanoic acid. 

A substantial portion of fhe gas and vapors emitted to the atmosphere in appreciable quantity from anthropogenic sources tends to be relatively simple in chemical structure carbon dioxide, carbon monoxide, sulfur dioxide, and nitric oxide from combustion processes hydrogen sulfide, ammonia, hydrogen chloride, and hydrogen fluoride from industrial processes. The solvents and gasoline fractions that evaporate are alkanes, alkenes, and aromatics with relatively simple structures. In addition, more complex... 

Mechanism The reaction of and A -steroids with nitrosyl fluoride to form ni trimines is best discussed in conjunction with the nitrosyl chloride reaction leading tothe5a-chloro-6 -nitro steroids (33). Since nitroso alkanes are oxidized with nitrosyl chloride to nitro alkanes it is believed that 5a-chloro-6j5-nitro steroids are formed in this way from an initially formed 5a-chloro-6 -nitroso adduct. The same is true for nitrosyl fluoride up to the stage of the nitroso fluoride (56). Since NOF is a weaker oxidizing agent than NOCl the nitroso fluoride tautomerizes to the fluoro oxime (57) at a rate... 

Deep fluorinalion of alkanes, ethers, acid fmlides, esters, alkyl chlorides, most ketones, ketals, orthoesters, and combinations of these functional groups produces principally the perfluonnated analogues (Table 2) Chlorine substituents (or chloro groups) usually survive fluorination... 

Chlorine gas reacts directly and highly exothermically with alkanes, giving rise to alkyl chlorides and hydrogen chloride, e.g., for addition to methane. 

Wojtkonski [185] has also reported on three series of melt spinnable thermotropic aromatic-aliphatic polyimines. The polyimines were prepared by reaction of 1,2-bis(4-formylphenoxy) ethane, terephthalaldehyde, or 4,4 -biphenyldicarboxaldehyde, respectively, with l,n-bis(4-amino-3-methylphenoxy) alkanes where n = 1-10, 12, 14, and 16 in dry DMAC containing 5% dry lithium chloride. The polymers decomposed at 400°C, and as the length of the flexible aliphatic segments increased, melting points decreased. Polymers with an odd... 

I Substitution reactions occur when two reactants exchange parts to give two new products. An example is the reaction of an alkane with Cl2 in the presence of ultraviolet light to yield an alkyl chloride. A Cl atom from Cl2 substitutes for an H atom of the alkane, and two new products result. 

Infrared radiation, electromagnetic spectrum and, 419, 422 energy of. 422 frequencies of, 422 wavelengths of, 422 Infrared spectroscopy, 422-431 acid anhydrides, 822-823 acid chlorides, 822-823 alcohols. 428, 632-633 aldehydes, 428. 730-731 alkanes, 426-427 alkenes, 427 alkynes, 427 amides. 822-823 amines, 428, 952 ammonium salts, 952-953 aromatic compound, 427-428, 534 bond stretching in, 422... 

The complex 8, formed by the addition of 2-propenylmagnesium chloride to 7, adds to aromatic aldehydes, 1-alkanals, a-branched and unbranched alkanals uniformly from the 7 c-face leading to hoinoallylic alcohols with 88-94% ee35 (Method A). After hydrolytic workup, both components can be recycled. Allyl complexes 10, generated from 9, prefer 67-attack and lead to the ent-homoallylic alcohols with excellent enantioselectivity36 (Method B) (Table 8). 

Sulfmyl radicals have also been invoked in the synthetically useful reaction of alkane-and arenesulfinyl chlorides with activated zero-valent metals (Ag, Cu, Zn) to give the corresponding symmetrical thiosulfonates21. 

Although reaction 6 is essentially a diffusion-controlled process for all kinds of substituents, the small differences observed in the rate constants through the series alkane-, amino- and alkoxy-sulfonyl chlorides have been attributed to the increased importance of polar effects to the transition state11. 

Typically, the saponification is run with 10% sodium hydroxide solution in a reactor cascade at 95-98°C under stringent pH control. The saponification mixture is separated in a settler. The upper phase consists of alkanes with a small proportion of chloroalkanes, which is removed by oleum refining or dehydrochlorination and high-pressure hydrogenation. The refined alkanes can be recycled to the reactor. In the aqueous lower phase are alkanesulfonates, sodium chloride, and between 4 and 8 wt % hydrotropically dissolved alkanes. An optimal separation can be approached at 95 °C, and residence times of less than 60 min if Fe(III) ions are added and pH values of 3-5 are maintained. 

After cooling of the aqueous mixture to 5-10°C an upper viscous phase is separated, which contains 45-47% alkanesulfonates and 1.0-1.3% sodium chloride, while the lower phase is a 7-8% brine with a small quantity of alkane-monosulfonates but 1.5-2.0 wt % di- and polysulfonates. The hydrotropically dissolved alkanes (neutral oil) are found entirely in the upper phase. Because of the small density differences, the separation of the two phases needs 15-20 h. The lower phase can be separated by membrane technology [13]. 

Impurities consist of unreacted material, including alkanes and internal or branched alkenes, and other material which can be detected in the neutral oil fraction of AOS. Examination of this fraction also indicates the amount of unhydrolyzed material (sulfonate esters and sultones) and byproducts (secondary alcohols, unsaturated and 2-chloro-y-sultones) in the sample. Salt calculations are made to determine inorganic sulfates and sodium chloride. Determinations for alkalinity, color, and water are required to meet product... 

A solution of sample in carbon tetrachloromethane is injected directly into the column and alkane- and monochloroalkanesulfonyl chloride determined as chloroalkane and dichloroalkane, respectively. 

The injected sulfonyl chlorides decompose instantaneously to give peaks of monochloroalkanes and 1-alkenes from alkanesulfonyl chlorides and dichloro-alkanes, and monochloro- 1-alkenes from monochloroalkane sulfonyl chlorides ... 

Nitro-olefine werden von Zinn(II)-chlorid in waBrigem Methanol zu einem Ge-misch aus Nitro-alkan und Oxim (s. Bd. X/4, S. 153) reduziert. 

Vicinale Dihalogen-alkane lassen sich durch das System Titan(III)-chlorid/Lithiumala-nat bzw. Titan(IV)-chlorid/Lithiumalanat unter Eliminierung der Halogen-Atome in guten Ausbeuten zu Alkenen reduzieren (die Ausbeuten liegen hoher als bei den Reduk-tionen mit Zink und die Reaktion verlauft einfacher als mit Natrium in flussigem Ammo-niak)7 ... 

Bei Alkanal-acetalen wird bei der Reduktion mit Titan(IV)-chlorid/Lithiumalanat se-lektiv eine Alkoxy-Gruppe reduktiv entfernt3 z. B. ... 

Auch primare und sekundare Nitro-alkane werden durch Chrom(II)-chlorid iiber die Imine in die entsprechenden Carbonyl-Verbindungen umgewandelt1 ... 

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