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Bromine ion

Kinetic studies of molecular bromination have been carried out using a variety of solvents other than acetic acid. The bromination of 2-nitroanisole by bromine in water revealed that molecular bromine is the reactive species and that the tribromide ion is very unreactive191. By making allowance for the concentration of free bromine (which differs from the stoichiometric concentration through reaction with bromine ion), good second-order rate coefficients were obtained by application of equation (133) with k2 = 0.062 at 25 °C the dominance of the bimolecular mechanism is to be expected here in view of the trend observed on making acetic acid media more aqueous. [Pg.120]

For the determination of bromine ions add to the solution 5-10 drops of a 0-1 per cent aqueous solution of eosin sodium. In this... [Pg.75]

No bromine ion is liberated when the analogous experiment is performed with bromobenzene (next preparation). Distinction between halogen in aliphatic and aromatic combination. [Pg.103]

Pure bromobenzene loses no bromine ions when boiled with potassium hydroxide solution. Check this. [Pg.105]

The relationships between rate of cleavage, bond strength and radical-anion redox potential can be combined in one concept. In this, cleavage rate is dependent on a reaction driving force, defined as the difference between the redox potential of the substrate radical-anion and the redox potential of the product anion in equ-librium with the coiresponding radical (E° for bromine ion, bromine radical as an example). [Pg.94]

TABLE 8.14 Aqueous-Phase Chemistry Involving S(IV) and Reactive Chlorine and Bromine Ions... [Pg.321]

Also two salts are known of molecular formula Co(NH3)5Br(S04) one is reddish violet in colour, and a freshly prepared aqueous solution contains sulphate ions the other is red in colour, and a freshly prepared aqueous solution contains bromine ions but no sulphate ions. The former substance is bromo-pentammino-cobaltie sulphate, [Co(NH3)5Br]S04 the latter is sulphato-pentammino-cobaltie bromide, [Co(NH3)5S04]Br.2 It is interesting to note that in the second compound the sulphate radicle occupies one co-ordinate position, but it also requires two principal valencies, and thus the complex ion is monovalent. [Pg.130]

Ionic crystals can form solid solutions, too. KBr, in the presence of KG1, will form crystals, in which some of the Br ions are substituted by Cl ions. If KC1 is in excess, a KC1 crystal is formed with some of the chlorine ions replaced by bromine ions. Smaller ions, like F , or larger, like I"", do not replace Br ions in KBr in considerable quantities KF and KBr do not form solid solutions, unless at high temperature or between very narrow limits. In chloride bromide systems the composition of the solid solution may range from pure chloride to pure bromide. [Pg.97]

What gets reduced as bromine ions, Br, on photographic film are oxidized by light ... [Pg.383]

Trimethyl tellurium bromide, (CH3)3TeBr, is obtained from the /3-base and hvdrobromic acid. It forms large, transparent, colourless tablets, slowly decomposing between 250° and 280° C., readily soluble in cold water but almost insoluble in organic solvents. The neutral solution in water contains bromine ions, and gives no precipitate or coloration with colourless hydriodic acid. It unites with ferric chloride. giving a complex which crystallises as salmon-coloured needles and forms a complex salt with stannic bromide. [Pg.174]

When the alcohol is protonated by the hydrobromic acid, the attached bromine attacks the adjacent carbon, ejecting the leaving group to form a bromonium ion. The bromine ion is then equally likely to attach via pathway a or b in Figure I. Both the formation of the bromonium ion and attachment of the bromine ion are similar to an N2 mechanism where attachment of the nucleophile and detachment of the leaving group occur in a single step. [Pg.111]

I > is correct. The bromine ion is a negatively charged intermediate looking for a positive charge. Question What s a halophile Answer Who cares No one taking the MCAT. Answer choice A is a trap. [Pg.131]

This formula is not intended to show that the acetone acts directly as a depolarizer of the bromine ion. The reaction mechanism has not yet been completely elucidated. [Pg.72]

On the reaction of halogen with butadiene both 1,4 and 1,2 addition occur simultaneously. The first step is again the reaction with a positive bromine ion with butadiene in configuration I (or III p. 215) leading to the resonating configurations ... [Pg.263]

One of the simplest reactions of a saturated molecule is the exchange between an alkyl bromide and a (radioactive) bromine ion. In this reaction Br + RBr—> BrR + Br the (radioactive) bromine atom is attached at the side opposite to the expelled atom since the reaction with an optically active alkyl bromide is associated with racemization (WALDEN-in-version). The transition state is, therefore, in this case a state with both bromine atoms at equal distances from the carbon atom and the three hydrogen atoms in a plane perpendicular... [Pg.264]

Remember the mnemonic device, An Ox, and that oxidation occurs at the anode. This means that the half reaction at the anode will show a loss of electrons. The negatively charged bromine ions will serve this purpose. The half reaction must also be written correctly as well. [Pg.255]

After the reaction is over the excess of bromine is boiled off, stirring to prevent local overheating, and the golden yellow solution is cooled and the volume measured. Bromine ion is then determined in an aliquot portion, after which the calculated amount of lead carbonate, ground to a thin paste with water, is added in small portions, with stirring. An appreciable excess of lead carbonate is to be avoided, as lead gluconate is... [Pg.59]


See other pages where Bromine ion is mentioned: [Pg.2750]    [Pg.83]    [Pg.1090]    [Pg.123]    [Pg.94]    [Pg.42]    [Pg.253]    [Pg.65]    [Pg.97]    [Pg.98]    [Pg.104]    [Pg.106]    [Pg.107]    [Pg.111]    [Pg.112]    [Pg.115]    [Pg.13]    [Pg.462]    [Pg.375]    [Pg.104]    [Pg.312]    [Pg.28]    [Pg.400]    [Pg.148]    [Pg.55]    [Pg.81]    [Pg.183]    [Pg.60]    [Pg.79]    [Pg.307]    [Pg.325]   
See also in sourсe #XX -- [ Pg.218 ]




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Bromination metal ions

Bromination pyridinium ions

Bromine with carboxylate ions

Bromine/ions/salts

Bromonium ions aromatic bromination

Bromonium ions, bromination

Bromonium ions, bromination without

Nucleophilic Displacement of Bromine or Chlorine Atoms with the Fluoride Ion

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