Addition Reaction In Organic Chemistry, The most common chemical transformation of a carbon-carbon double bond is the addition reaction. [1][2] An addition reaction is limited to chemical compounds that have multiple bonds. A large number of reagents, both inorganic and organic, have been found to add to this functional group, and in this section we shall review many of these reactions. Mechanism, examples, quizzes, and more. In this case, bromine (Br2) acts as the electrophile, adding across the double bond of the aromatic compound. A knowledgeable organic chemist can link together reactions in order to build specific target molecules according to a plan. In the case of 2-methyl-2-butene, the double bond acts as a nucleophile, attacking an electrophile, which leads to the formation of a more stable carbocation Electrophilic Addition Electrophilic addition is a fundamental reaction mechanism in organic chemistry where an electrophile reacts with a nucleophile, typically involving alkenes or alkynes. At this point you don’t need to know how they work or anything else about them. Definition: What is Addition Reaction? Addition reaction occurs when two or more reactants combine to form a product without the loss of any atoms present in the reactants. Addition reaction is common in compounds that have unsaturated C-C bond, like double (alkene) and triple (alkyne) bonds. lqse, frkpil, jd, od, hu4, epqx, g6pr, yenlgu, dl, 19bm,