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A halogen addition reaction is a simple organic reaction where a halogen molecule is added to the carbon–carbon double bond of an alkene functional group. [1] The general chemical formula of the halogen addition reaction is: C=C + X 2 → X−C−C−X (X represents the halogens bromine or chlorine, and in this case, a solvent could be CH 2 ...
Illustrative of the bromination of an alkene is the route to the anesthetic halothane from trichloroethylene: [6] 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.
General overview of addition reactions. Top to bottom: electrophilic addition to alkene, nucleophilic addition of nucleophile to carbonyl and free-radical addition of halide to alkene. Depending on the product structure, it could promptly react further to eject a leaving group to give the addition–elimination reaction sequence.
Alkenes reliably add bromine without catalysis to give the vicinal dibromides: RCH=CH 2 + Br 2 → RCHBrCH 2 Br. Aromatic compounds undergo bromination simultaneously with evolution of hydrogen bromide. Catalysts such as AlBr3 or FeBr3 are needed for the reaction to happen on aromatic rings.
In addition, bromine water is commonly used to test for the presence of an alkene which contains a double covalent bond, reacting with the bromine water, changing its color from an intense yellow to a colorless solution. Bromine water is also commonly used to check for the presence of an aldehyde group in compounds. In this reaction, the color ...
In organic chemistry, syn-and anti-addition are different ways in which substituent molecules can be added to an alkene (R 2 C=CR 2) or alkyne (RC≡CR).The concepts of syn and anti addition are used to characterize the different reactions of organic chemistry by reflecting the stereochemistry of the products in a reaction.
The year’s surprise sensation, Alison Espach’s improbably fun novel follows the adventures of a severely bummed out young woman who finds herself accidentally crashing a lavish wedding at a ...
Adding the hydrogen ion to one carbon atom in the alkene creates a positive charge on the other carbon, forming a carbocation intermediate. The more substituted the carbocation, the more stable it is, due to induction and hyperconjugation. The major product of the addition reaction will be the one formed from the more stable intermediate.