4.1.3 alkenes Flashcards
what is a sigma bond
when 2 s-orbitals directly overlap
what is a pi bond
sideways overlap of two p orbitals
draw diagram
in booklet
what is the bond angle in alkene
120 as there are 3 bonding regions of electrons which repel one another equally
what is a structural isomer
same molecular formula but different structural formula
what is stereoisomerism
same structural formula but different arrangements of atoms in space
what must a compound have for it to have E/Z isomerism
(type of stereoisomerism)
-a c=c double bond
-each carbon must have two different groups attached to it
e isomer
high priority groups are on the opposite side
z isomer
high priority groups are on the same side
cis/trans
each carbon has one of the same groups
cis
same group is on the same side
trans
same group is on the opposite sides
are alkenes or alkanes more reactive
alkenes as the pi bond has a lower bond enthalpy than the sigma bond
alkene to alkane
add H2
-nickel catalyst, 150 degrees
alkene to haloalkane
-add hydrogen halide
-NOTE- if alkene is unsymmetrical two products are possible
alkene to alcohol
-Add H2O (steam)
-phosphoric acid catalyst, 60 atm, 300 degrees
testing for alkene
add bromine water
-decolourises from orange to colourless
electrophile
electron pair acceptor
heterolytic fission
breaking of a covalent bond so both electrons from the bond go to one atom
curly arrows
show the movement of electron pairs
what is the mechanism for an alkene called
electrophilic addition
which carbocation is more stable and what does this mean about the amount of product formed
secondary carbocation intermediate is more stable than a primary carbocation intermediate
so more product is formed from a secondary carbocation intermediate
how do simple monomer alkenes join together
simple monomer alkenes join together to form long chain polymers
the pi bond breaks to form new sigma bonds
conditions for addition polymerisation
high pressure and a catalyst