alkenes Flashcards
1
Q
Describe alkenes
A
- unsaturated which means there is at least 1 = covalent bond
- can undergo addition reactions
- = have a high e- density making them reactive
2
Q
what are sigma bonds
A
- are when 2s orbitals overlap
- align horizontally to give a single covalent bond
- strong electrostatic attraction between the nuclei of the shared pair of electrons (bc of high electron density between the nuclei)
- high bond enthalpy
- strongest type of covalent bond
3
Q
what are pi bonds
A
- sideways overlap of 2 p orbitals above and below the C=C.
- PB are weaker than SB bc the e- density is spread out above and below the nuclei
- electrostatic attraction is weaker so SB have a lower bond enthalpy
- PB locks the 2 C-atoms in position and prevents them from rotating around the =, so rotation is restricted.
4
Q
describe the reactivity of alkenes
A
- alkenes have SB + PB
- 3/4 used in SB.
- this is a high electron density area that makes them reactive
- PB stick out a little and the = has a high ED
- open to attack from electrophiles
- PB has a low bond enthalpy so alkenes are reactive bc not a lot of energy needed
5
Q
shape of alkenes
A
- trigonal planar
- three regions of e- density around each carbon atom
- three regions repel AFAP
- bond angle is 120
6
Q
stereoisomers
A
- same structural formula
- different arrangement of atoms in space
- e/z isomerism occurs when there is restricted rotation around = and requires 2 diff FG attached to each c-atom
- E + trans= opposite
- Z + cis- same side
7
Q
describe the Cahn Inlog Prelog rules
A
- when there are 4 diff groups around a double bond
- priority based on their atomic number
- calculate the atomic number of the first element directly bonded to C=C.
- if first element is the same number, move down the chain .
8
Q
describe test for alkenes
A
- decolourisation of Br water
- adding Br water to alkenes causes a colour change from brown/orange to colourless
- Br is the electrophile and adds to the alkene forming dibromo alkane
- Br2 is polarised as the e- in the = repels the e- in Br2
- Br(-)-(Br(+)
- Br2 bond breaks by heterolytic fission
- double bond breaks
- one carbon bonds to a Br
- carbocation intermediate is formed and a Br- with 2 electrons
- addition product formed
9
Q
what is an electrophile
A
- electron pair acceptor
- deficient in electrons so are attracted to a =
- H+ , NO2+
- E.g polar molecules (delta+) H-Br
10
Q
Hydration of alkenes
A
- alcohol is formed
- sue steam and acid catalyst to create and alcohol
- can make ethanol by reacting steam and ethene using a phosphoric acid catalyst + 300C + 60atm
11
Q
addition of hydrogen halides to alkenes
A
- electrophilic addition
- halogenoalkanes formed,
12
Q
reaction of alkenes with unsymmetrical hydrogen halide
A
- 2 different products are formed
- the more stable carbocation forms the major product
- the less stable carbocation forms the minor product
13
Q
what determines the stability of a carbocation
A
- the more alkyl groups bonded to carbocation the more stable
- bc alkyl groups push e- towards the +ve carbocation stabilising it
14
Q
describe addition polymers
A
- alkenes are the monomers which join to form addition polymers
- natural : proteins and natural rubber
- synthetic : poly(ethene) and poly(propene)
15
Q
how to make poly(propene)
A
- need several monomers of propene
- the double bond opens up to form the polymer
- the monomer will have a bracket around it
- each carbon will have no = and a single bond coming out of the bracket to form 4 bonds
- poly(alkanes) are saturated, normally non-polar and unreactive.
- they don’t degrade well in landfill.