One of the features that makes the hydroboration reaction so useful is the regiochemistry that results when an unsymmetrical alkene is hydroborated. For example, hydroboration-oxidation of 1-methylcyclopentene yields trans-2-methylcyclopentanol. Boron and hydrogen add to the alkene with syn stereochemistry, with boron attaching to the less highly substituted carbon. During the oxidation step, the boron is replaced by a hydroxyl with the same stereochemistry, resulting in an overall syn non-Markovnikov addition of water. This stereochemical result is particularly useful since it is complementary to the Markovnikov regiochemistry observed for oxymercuration.