Addition to Unsymmetrical Alkenes (HL) (DP IB Chemistry)

Addition to Unsymmetrical Alkenes

• Carbocations are positively charged carbon atoms with only three covalent bonds instead of four

• There are three types of carbocations: primary, secondary and tertiary

Inductive effect

• The alkyl groups attached to the positively charged carbon atoms are ‘electron donating groups’

  • This is also known as the inductive effect of alkyl groups

• The inductive effect is illustrated by the use of arrowheads on the bonds to show the alkyl groups pushing electrons towards the positively charged carbon

  • This causes the carbocation to become less positively charged

• As a result of this, the charge is spread around the carbocation which makes it energetically more stable

• This means that tertiary carbocations are the most stable as they have three electron-donating alkyl groups which energetically stabilise the carbocation

• Due to the positive charge on the carbon atom, carbocations are electrophiles

Primary, secondary and tertiary carbocations

Alkyl groups push electron density towards the carbocation making it energetically more stable; the more alkyl groups the carbocation is bonded to, the more stabilised it is

Markovnikov’s rule

• Markovnikov’s rule predicts the outcome of electrophilic addition reactions and states that:

  • In an electrophilic addition reaction of a hydrogen halide (HX) to an alkene, the halogen ends up bonded to the most substituted carbon atom

  • In an electrophilic addition reaction of an interhalogen to an alkene, the most electronegative halogen ends up bonded to the most substituted carbon atom

• Markovnikov addition applies to electrophilic addition reactions with unsymmetrical alkanes, e.g. propene and but-1-ene

  • Markovnikov addition favours the formation of the major product

  • Anti-Markovnikov addition favours the formation of the minor product

• In electrophilic addition reactions, an electrophile reacts with the double bond of alkenes (as previously discussed)

• The mechanism for electrophilic addition reactions with unsymmetrical alkenes is slightly different, e.g. propene + hydrogen bromide

Step 1 in the electrophilic addition mechanism

The electrophile reacts with the electron-rich C-C double bond

• The electrophile can attach in two possible ways:

  1. Breaking the C=C bond and attaching to the least substituted carbon

     • This will give the most stable carbocation as an intermediate that will form the major product

  2. Breaking the C=C bond and attaching to the most substituted carbon

     • This will give the least stable carbocation as an intermediate that will form the minor product

Relative stabilities of primary and secondary carbocations

The major and minor carbocation intermediates formed during the reaction of propene and hydrogen bromide

• The nucleophile will bond to the positive carbon atom of the carbocation

• The more stable carbocation produces the major product

• The less stable carbocation produces the minor product

Formation of major and minor products

Formation of the major and minor products of the reaction of propene with hydrogen bromide

• The mechanism for the electrophilic addition of hydrogen bromide to propene, showing the formation of the major and minor products can be shown as:

Electrophilic addition mechanism showing the formation of the major and minor products

The electrophilic addition reaction mechanism of HBr and propene to form 1-bromopropane and 2-bromopropane