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The general chemical equation for the hydration of alkenes is the following: RRC=CH 2 + H 2 O → RRC(OH)-CH 3. A hydroxyl group (OH −) attaches to one carbon of the double bond, and a proton (H +) adds to the other. The reaction is highly exothermic. In the first step, the alkene acts as a nucleophile and attacks the proton, following ...
A distinct exothermic reaction makes a reactant "spring-loaded". ... The tetrazole-alkene "photoclick" reaction is another dipolar addition that Huisgen first ...
The hydrogenation of alkenes to alkanes is exothermic.The amount of energy released during a hydrogenation reaction, known as the heat of hydrogenation, is inversely related to the stability of the starting alkene: the more stable the alkene, the lower its heat of hydrogenation.
In organosulfur chemistry, the thiol-ene reaction (also alkene hydrothiolation) is an organic reaction between a thiol (R−SH) and an alkene (R 2 C=CR 2) to form a thioether (R−S−R'). This reaction was first reported in 1905, [ 1 ] but it gained prominence in the late 1990s and early 2000s for its feasibility and wide range of applications.
During alkyl radical disproportionation, an alkane and an alkene are the end products and the bond order of the products increases by one over the reactants. [1] Thus the reaction is exothermic (ΔH = 50–95 kcal/mol (210–400 kJ/mol)) and proceeds rapidly. [6]
As alkenes can polymerize in somewhat straightforward radical reactions, they form useful compounds such as polyethylene and polyvinyl chloride (PVC), [3] which are produced in high tonnages each year [3] due to their usefulness in manufacturing processes of commercial products, such as piping, insulation and packaging.
An overall process of disproportionation can be observed, where "light", hydrogen-rich products are formed at the expense of heavier molecules which condense and are depleted of hydrogen. The actual reaction is known as homolytic fission and produces alkenes, which are the basis for the economically important production of polymers. [6]
Ozone adds across the carbon–carbon double bond of the alkene to form a molozonide, which then decomposes to produce a carbonyl (RR'CO) and a carbonyl oxide. The latter is known as the Criegee intermediate. [8] The alkene ozonolysis reaction is extremely exothermic, releasing about 50 kilocalories per mole (210 kJ/mol) of excess energy.