Bromide aluminum reaction with bromine

Photochlorination of tetrachloroethylene, observed by Faraday, yields hexachloroethane [67-72-1]. Reaction with aluminum bromide at 100°C forms a mixture of bromotrichloroethane and dibromodichloroethane [75-81-0] (6). Reaction with bromine results in an equiUbrium mixture of tetrabromoethylene [79-28-7] and tetrachloroethylene. Tetrachloroethylene reacts with a mixture of hydrogen fluoride and chlorine at 225—400°C in the presence of zirconium fluoride catalyst to yield l,2,2-trichloro-l,l,2-trifluoroethane [76-13-1] (CFG 113) (7). 

Mole ratios You have seen that the coefficients in a chemical equation indicate the relationships among moles of reactants and products. For example, return to the reaction between iron and oxygen described in Table 12-1. The equation indicates that four moles of iron react with three moles of oxygen. It also indicates that four moles of iron react to produce two moles of iron(III) oxide. How many moles of oxygen react to produce two moles of iron(III) oxide You can use the relationships between coefficients to write conversion factors called mole ratios. A mole ratio is a ratio between the numbers of moles of any two substances in a balanced chemical equation. As another example, consider the reaction shown in Figure 12-2. Aluminum reacts with bromine to form aluminum bromide. Aluminum bromide is used as a catalyst to speed up a variety of chemical reactions. 

At 225—275°C, bromination of the vapor yields bromochloromethanes CCl Br, CCl2Br2, and CClBr. Chloroform reacts with aluminum bromide to form bromoform, CHBr. Chloroform cannot be direcdy fluorinated with elementary flourine fluoroform, CHF, is produced from chloroform by reaction with hydrogen fluoride in the presence of a metallic fluoride catalyst (8). It is also a coproduct of monochlorodifluoromethane from the HF—CHCl reaction over antimony chlorofluoride. Iodine gives a characteristic purple solution in chloroform but does not react even at the boiling point. Iodoform, CHI, may be produced from chloroform by reaction with ethyl iodide in the presence of aluminum chloride however, this is not the route normally used for its preparation. 

Allylmagnesium bromide, 41, 49 reaction with acrolein, 41, 49 5-Allyl-l,2,3,4,5-pentachlorocyclopen-tadiene, 43, 92 Allyltriphenyltin, 41, 31 reaction with phenyllithium, 41, 30 Aluminum chloride, as catalyst, for isomerization, 42, 9 for nuclear bromination and chlorination of aromatic aldehydes and ketones, 40, 9 as Friedel-Crafts catalyst, 41, 1 Amidation, of aniline with maleic anhydride, 41, 93... 

When the metallic additive to the intermediate 374 was zinc dihalide (or another Lewis acid, such as aluminum trichloride, iron trichloride or boron trifluoride), a conjugate addition to electrophilic olefins affords 381 . In the case of the lithium-zinc transmetallation, a palladium-catalyzed Negishi cross-coupling reaction with aryl bromides or iodides allowed the preparation of arylated componnds 384 ° in 26-77% yield. In addition, a Sn2 allylation of the mentioned zinc intermediates with reagents of type R CH=CHCH(R )X (X = chlorine, bromine) gave the corresponding compounds 385 in 52-68% yield. ... 

Reactions, e.g., with alkyl halides in ether using Ziegler-Natta catalyst form alkyl aluminum halides, R3AI2X3, [R2A1X]2 and [RA1X]2 with bromine vapor forms anhydrous aluminum bromide,... 

Exercise 22-14 Aluminum chloride is a much more powerful catalyst than ferric bromide for bromination of benzene. Would you expect the combination of aluminum chloride and bromine to give much chlorobenzene in reaction with benzene Explain. 

Thiiranes can be formed directly and stereospecifically from 1,2-disubstituted alkenes by addition of trimethylsilylsulfenyl bromide, formed at -78 C from reaction of bromine with bis(trimethylsilyl) sulfide (Scheme 7).12 A two-step synthesis of thiiranes can be achieved by addition of succinimide-A/-sulfe-nyl chloride or phthalimide-A -sulfenyl chloride to alkenes followed by lithium aluminum hydride cleavage of the adducts (Scheme 8).13 Thiaheterocycles can also be formed by intramolecular electrophilic addition of sulfenyl chlorides to alkenes, e.g. as seen in Schemes 914 and 10.13 Related examples involving sulfur dichloride are shown in Schemes 1116 and 12.17 In the former case addition of sulfur dichloride to 1,5-cyclooctadiene affords a bicyclic dichloro sulfide via regio- and stereo-specific intramolecular addition of an intermediate sulfenyl chloride. Removal of chlorine by lithium aluminum hydride reduction affords 9-thiabicyclo[3.3.1]nonane, which can be further transformed into bicyclo[3.3.0]oct-1,5-ene.16... 

Aluminum bromide can be prepared by reacting small pieces of aluminum foil with liquid bromine at room temperature. The reaction is accompanied by flashes of red light. 

In a flask, 10.3 g of aluminum reacted with 100.0 g of liquid bromine to form aluminum bromide. After the reaction, no aluminum remained, and 8.5 grams of bromine remained unreacted. How many grams of bromine reacted How many grams of compound were formed ... 

In support of this hypothesis it has been observed that when aluminum bromide is treated with oxygen a reaction occurs which liberates bromine,48 and further, the halogen atoms rather than the hydroxyl group are responsible for the catalytic activity of HOAlBr2. Thus when the compound DOAlBr2 is prepared, the hydrogen-deuterium exchange with n-butane is not at all proportional to isomerization.4 ... 

Attempts to brominate benzo[h]quinolizinium bromide (3) with liquid bromine gave an addition product (Section II,B). Bromination with bromine and aluminum bromide in dimethylformamide gave 1 l-bromobenzo[b]-quinolizinium bromide (137).71 Sulfuryl chloride and aluminum chloride under similar reaction conditions gave the chlorobenzquinolizinone (139), presumably from the 6,11-dichlorobenzquinolizinium salt (138).71 Without... 

CARBINOL (67-56-1) Forms explosive mixture with air (flash point 50°F/10°C). Violent reaction with strong oxidizers, acetyl bromide, alkyl aluminum salts, beryllium dihydride, bromine, chromic acid, l-chloro-3,3-difluoro-2-methoxycyclopropene, cyanuric chloride, di-ethylzinc, isophthaloyl chloride, nitric acid, perchloric acid, potassium-fert-butoxide, potassium sulfur diimide, Raneynickel catalysts, 2,4,6-trichlorotriazine, triethylaluminum,... 

MERCURIO (Italian, Spanish) (7439-97-6) Violent reaction with alkali metals, aluminum, acetylenic compounds, azides, boron phosphodiiodide (vapor explodes), bromine, 3-bromopropyne, chlorine, chlorine dioxide, ethylene oxide, lithium, metals, methyl silane (when shaken in air), nitromethane, peroxyformic acid, potassium, propargyl bromide, rubidium, sodium, sodium carbide. Forms sensitive explosive products with acetylene, ammonia (anhydrous), chlorine, picric acid. Increases the explosive sensitivity of methyl azide. Mixtures with hot sulfuric acid can be explosive. Incompatible with calcium, sodium acetylide, nitric acid. Reacts with copper, silver, and many other metals (except iron), forming amalgams. 

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