6. reactions of alkenes Flashcards
what reactions happen to alkenes
electrophilic addition (dihaloalkane) hydrogenation (addition reaction) (alkane) steam hydration (alcohol)
during electrophillic addition reaction of an alkene what happens
double bond opens up
atoms added to carbon atoms
why do elecrophilic addition ractions happen to alkenes
double bond has lots of electrons and is easily attacked by electrophiles
what are electrophiles
electron-pair acceptors
usually short of electrons so attracted to electron rich areas
what do electrophiles include
positivley charged ions e.g. H+ and NO2+
polar molecules. atoms with positive dipole attracted toelectron rich areas
alkenes undergo hydrogenation to produce
alkanes
hydrogenation
- ethene reacts with ? to produce ?
- equation
- conditions
- hydrogen gas to produce ethane
- CH2CH2 + H2 -> CH3CH3
- nickel catalyst
electrophilic addition
- alkenes can react with halogens to form ?
- equation
- dihaloalkanes
2. CH2CH2 + X2 -> CH2XCH2X
what is a carbocation
an organic ion containing a positively charged carbon atom
how is bromine water used to test for Carbon carbon double bond
shake alkene with orange bromine water = solution decolourises
(bromine is added across double bond to form a colourless dibromoalkane)
steam hydration
- alkenes reacts with steam to make ?
- equation
- conditions
- alcohols
- CH2CH2(g) + H2O(g) CH3CH2OH(g)
- phosphoric (v) acid catalyst
steam hydration
- reaction yield high/low?
- is this a problem?
- low.
2. no. can recycle unreacted alkene gas
addition with hydrogen halides
- alkenes react with hydrogen halides to make ?
- equation
- haloalkanes.
2. CH2CH2 + HBr -> CH2BrCH3
markownikoffs rule
major product from addition of a hydrogen halide (HX) to an unsymmetrical alkene is one where H adds to the carbon with most Hs already attached
adding hydrogen halides to unsymmetrical alkenes
- what does the amount of each product formed depend on
- what carbocations are most stable and why
- which carbocation is most likely to form
- how stable the carbocation formed in the middle of the reaction
- carbocations with more alkyl groups because alkyl groups feed electrons towards positive charge.
- the more stable carbocation