Reaction of alkenes with H2 with metal catalyst

Reactions of Alkenes:
Electrophilic Additions
HBr
Br2
H2O/H+ >
KMnO4 H2O
H2 / Pt (metal)
The Formation of an Alkane
 

Here the alkene goes through a transfer of electrons as well as atoms, an example of reduction. Oxidation is always accompanied by oxidation and although the metal is not formally oxidized, its ease of access to oxidative steps allows the reaction to take place. Here, the alkene gains bonds to hydrogen and clearly is reduced. Since there are electrons being transferred, we cannot draw reaction paths very easily. There is still a useful picture that explains the chemistry of this reaction quite well. Most chemists imagine that the H-H on the metal surface is synchronously joined to the carbons of the double bond. Hydrogenation, the reaction of hydrogen gas with alkenes, is most famous in the saturation of some unsaturated fats. The unsaturated fats tend to be cis alkenes which cause their structure to be kinked. This kink causes the fat to be an oil. In order to get this molecular kink out of the molecule, we hydrogenated the fat causing the surface area to be more regular and the melting point of the fat is raised. Triolein is a triacylglycerol which is a liquid oil. Tristerin is a triacylglycerol that is solid. Not all double bonds get reduced in this process and some of the double bonds are isomerized to the trans isomer, which has a more regular shape and contributes to the solidifying of the oil. However, the trans alkene is metabolized differently than the cis and has been linked to raising the amount of cholesterol in the body, raising the danger of heart disease.