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For example, ethene + bromine → 1,2-dibromoethane: C 2 H 4 + Br 2 → BrCH 2 CH 2 Br. This takes the form of 3 main steps shown below; [3] Forming of a π-complex The electrophilic Br-Br molecule interacts with electron-rich alkene molecule to form a π-complex 1. Forming of a three-membered bromonium ion
The bromide ion acquires a positive formal charge. At this moment the halogen ion is called a "bromonium ion" or "chloronium ion", respectively. When the first bromine atom attacks the carbon–carbon π-bond, it leaves behind one of its electrons with the other bromine that it was bonded to in Br 2. That other atom is now a negative bromide ...
Ethane can react with the halogens, especially chlorine and bromine, by free-radical halogenation. This reaction proceeds through the propagation of the ethyl radical: [36] Cl 2 → 2 Cl• C 2 H 6 • + Cl• → C 2 H 5 • + HCl C 2 H 5 • + Cl 2 → C 2 H 5 Cl + Cl• Cl• + C 2 H 6 → C 2 H 5 • + HCl
Iodination and bromination can be effected by the addition of iodine and bromine to alkenes. The reaction, which conveniently proceeds with the discharge of the color of I 2 and Br 2, is the basis of the analytical method. The iodine number and bromine number are measures of the degree of unsaturation for fats and other organic compounds.
An element in a free form has OS = 0. In a compound or ion, the sum of the oxidation states equals the total charge of the compound or ion. Fluorine in compounds has OS = −1; this extends to chlorine and bromine only when not bonded to a lighter halogen, oxygen or nitrogen. Group 1 and group 2 metals in compounds have OS = +1 and +2 ...
Since phenols are acidic, they readily react with a strong base like sodium hydroxide to form phenoxide ions. The phenoxide ion will then substitute the –X group in the alkyl halide, forming an ether with an aryl group attached to it in a reaction with an S N 2 mechanism. C 6 H 5 OH + OH − → C 6 H 5 –O − + H 2 O C 6 H 5 –O − + R ...
NBS reacts with alkenes in aqueous solvents to give bromohydrins. The preferred conditions are the portionwise addition of NBS to a solution of the alkene in 50% aqueous DMSO, DME, THF, or tert-butanol at 0 °C. [3] Formation of a bromonium ion and immediate attack by water gives strong Markovnikov addition and anti stereochemical selectivities ...
The anion reacts with bromine in an α-substitution reaction to give an N-bromoamide. Base abstraction of the remaining amide proton gives a bromoamide anion. The bromoamide anion rearranges as the R group attached to the carbonyl carbon migrates to nitrogen at the same time the bromide ion leaves, giving an isocyanate.