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  2. Bromocyclohexane - Wikipedia

    en.wikipedia.org/wiki/Bromocyclohexane

    Uses and reactions It is used to match ... Bromocyclohexane can be prepared by the free radical bromination of cyclohexane. Safety. Bromocyclohexane is an alkylating ...

  3. Halogen addition reaction - Wikipedia

    en.wikipedia.org/wiki/Halogen_addition_reaction

    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 ...

  4. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    Cyclohexane is a colourless, flammable liquid with a distinctive detergent-like odor, reminiscent of cleaning products (in which it is sometimes used). Cyclohexane is mainly used for the industrial production of adipic acid and caprolactam, which are precursors to nylon. [5] Cyclohexyl (C 6 H 11) is the alkyl substituent of cyclohexane and is ...

  5. Bromine - Wikipedia

    en.wikipedia.org/wiki/Bromine

    Bromine addition to alkene reaction mechanism. An old qualitative test for the presence of the alkene functional group is that alkenes turn brown aqueous bromine solutions colourless, forming a bromohydrin with some of the dibromoalkane also produced. The reaction passes through a short-lived strongly electrophilic bromonium intermediate.

  6. Dehalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehalogenation

    In organic chemistry, dehalogenation is a set of chemical reactions that involve the cleavage of carbon-halogen bonds; as such, it is the inverse reaction of halogenation. Dehalogenations come in many varieties, including defluorination (removal of fluorine ), dechlorination (removal of chlorine ), debromination (removal of bromine ), and ...

  7. Hofmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Hofmann_rearrangement

    The symmetrical structure [clarification needed] of α-phenyl propanamide does not change after Hofmann reaction. In the synthesis of gabapentin, beginning with the mono-amidation of 1,1-cyclohexane diacetic acid anhydride with ammonia to 1,1-cyclohexane diacetic acid mono-amide, followed by a Hofmann rearrangement [12]

  8. Cyclohexene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene

    Cyclohexene is most stable in a half-chair conformation, [11] unlike the preference for a chair form of cyclohexane. One basis for the cyclohexane conformational preference for a chair is that it allows each bond of the ring to adopt a staggered conformation. For cyclohexene, however, the alkene is planar, equivalent to an eclipsed conformation ...

  9. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    The bromine test can also be used as an indication of the degree of unsaturation for unsaturated hydrocarbons. Bromine number is defined as gram of bromine able to react with 100g of product. [18] Similar as hydrogenation, the halogenation of bromine is also depend on the number of π bond. A higher bromine number indicates higher degree of ...