pi bonds are formed by electrons in the adjacent p-orbitals overlapping above and below the carbon atoms
-> this bond can only be made after a sigma bond has been formed
the pi bond holds the atoms in position by restricting rotation around the double bond so alkene molecules have a flat shape in the region of the double bonds - they are described as planar
the pi bond is the reactive part of the molecule because of the high electron density around it
alkene double bond shape and bond angle are trigonal planar and 120 degrees
alkenes are more reactive than alkanes due to high electron density of the double bond + the fact the pi bond is slightly easier to break
intermolecular forces of alkenes are only alkenes due to non-polar nature of the double bond
alkenes are insoluble in water because they have a double bond between carbon atoms which are non-polar bonds
types of isomers that can be formed using alkenes are :
E/Z isomers due to restricted rotation
Cis-trans isomers if two of the same substituents are attached to each carbon
most stable type of carbocation intermediate are alkyl groups as they have a positive inductive effect, so the most stable carbocation is the one bonded to the most other carbon atoms
e.g. a tertiary carbocation
major products will be formed from tertiary carbocations (or the most stable available
Carbocation
An electrically charged species that contains a positively charged carbon atom. Can be primary, secondary, or tertiary.
Stability
The tendency of a carbocation to persist without undergoing further reaction. A more stable carbocation is less reactive and persists for a longer time.
Inductive effect
A phenomenon in which the electrons in a bond are attracted towards a more electronegative atom. In carbocations, the positive charge on the carbon atom leads to a positive inductive effect, which stabilizes the carbocation.
Alkyl groups
Have the most positive inductive effect among carbocations, since they have a greater number of carbon atoms bonded to the positively charged carbon. This makes them more stable.
Tertiary carbocation
A carbocation with three other carbon atoms bonded to the positively charged carbon. It is more stable than secondary or primary carbocations due to the positive inductive effect.