cyclohexane and bromine reaction mechanism

: 16in a normal case, away from light, the reaction wont happen. this is because cyclohexane has no pi-unsaturation and therefore not nucleophilic. but5In absence of sunlight ( mostly UV light ) no reaction , but in presence of sunlight ( mostly UV light )free radical substitution reaction takes pl7If you simply coine [math]Br_2[/math] and cyclohexane in the dark, you will have no reaction. If you throw in a strong Lewis Acid like [math]AlBr15Nothing, but with cycloHEXENE, here is a reaction. This is due to the double bonds in the cyclohexene which break to allow the bromine to bond to i10There are two types of conditions in ur question.. 1) when there is no sunlight.. There will not be any reaction as there is no pi unsaturated bond1in a normal case, away from light, the reaction wont happen. this is because cyclohexane has no pi-unsaturation and therefore not nucleophilic. but5There are two types of conditions in ur question.. 1) when there is no sunlight.. There will not be any reaction as there is no pi unsaturated bond1Via free rsdical substituition reaction in presence of ultra violet light. Hydrogen atoms from cyclohexane are substituted by bromine atoms to form0No reaction is shown until the mixture is not treated with ultraviolet radiation. the reaction would result into bromo-cyclohexane and HBr. The rea0Cyclohexane reacts with bromine by radical mechanism to produce brom-substituted compounds on the light : C6H12 + Br2 - C6H11Br + HBr or at the hi1What is the chemical equation of the reaction between 2018916What is the mechanism for the reaction of cyclohexane with bromine in the pre… Hydrochloric acid manufacture2014815NICKEL CHLORIDE HEXAHYDRATE2011692-methylcyclohexanol dehydration product NMR2009218making sodium bromide20081122