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alkenes have p-orbitals defining the
second bond, with electron density above and below the trigonal planar molecule
addition reactions occur from
top or bottom faces
hydrogenation
the addition of H2
what does hydrogenation allow
Preparation of saturated hydrocarbons from alkenes
metal catalysts faciliate the
reaction in heterogeneous conditions with solid catalyst
more stable alkenes have lower heats of
hydrogenation because they start with less PE
Pi electrons create regions of
high electron density above and below the trigonal planar carbons making alkenes nucleophilic
electrophiles have regions of
positive charge that react with nucleophilic double bonds
Markovnikov’s rule
hydrogen adds to the carbon with more hydrogens
Markovs rule reflects
carbocation stability which generates the most susbituted carbocation
Achiral reagents give
a chiral products
Hydration of alknes can occur via
formation of h30 with a strong acid
each step is fully
reversible
hydration and dehydration are
two sides of an equilibrium
le chateliers principle
removing volatile alkenes drives elimination