Answer :
Three possible monohalogenation products for this reaction are (Z)-2-bromohex-2-ene, (R)-3-bromo-3-methylcyclohex-1-ene, and (1R,4R)-1,4-dibromocyclohexane.
A substance can be monohalogenation chemically by adding one or more halogens to it. This type of transformation is essential for the production of polymers and pharmaceuticals, among other things, due to the extensive occurrence of compounds containing halides. [1] In fact, this kind of conversion happens so frequently that it is challenging to give a whole explanation. This article's main focus is on how elemental halogens are used in halogenation (F2, Cl2, Br2, I2). Halogen acids and halide salts are commonly used to introduce halides. For the purpose of adding halogens to diverse substrates, including thionyl chloride, a wide range of specialized reagents are available. There are several ways to halogenate organic molecules, including the halogen addition process, electrophilic halogenation, free radical halogenation, and ketone halogenation. The substrate's characteristics determine the route. The halogen has an impact on the halogenation facility. Fluorine and chlorine are more vigorous halogenating agents and are more electrophilic. Iodine is the least reactive of all the halogenating agents, while bromine is weaker than both fluorine and chlorine.
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