# Electrophilic Addition of Hydrogen Halides II


Symmetrical alkenes (like ethene or but-2-ene) are dealt with first. These are alkenes where identical groups are attached to each end of the carbon-carbon double bond.

All alkenes undergo addition reactions with the hydrogen halides. A hydrogen atom joins to one of the carbon atoms originally in the double bond, and a halogen atom to the other. For example, with ethene and hydrogen chloride, you get chloroethane:

With but-2-ene you get 2-chlorobutane:

What happens if you add the hydrogen to the carbon atom at the right-hand end of the double bond, and the chlorine to the left-hand end? You would still have the same product. The chlorine would be on a carbon atom next to the end of the chain - you would simply have drawn the molecule flipped over in space. That would be different of the alkene was unsymmetrical - that's why we have to look at them separately.

### Conditions

The alkenes react with gaseous hydrogen halides at room temperature. If the alkene is also a gas, you can simply mix the gases. If the alkene is a liquid, you can bubble the hydrogen halide through the liquid. Alkenes will also react with concentrated solutions of the gases in water. A solution of hydrogen chloride in water is, of course, hydrochloric acid. A solution of hydrogen bromide in water is hydrobromic acid - and so on. There are, however, problems with this. The water will also get involved in the reaction and you end up with a mixture of products.

### Reaction rates

Reaction rates increase in the order HF - HCl - HBr - HI. Hydrogen fluoride reacts much more slowly than the other three, and is normally ignored in talking about these reactions. When the hydrogen halides react with alkenes, the hydrogen-halogen bond has to be broken. The bond strength falls as you go from HF to HI, and the hydrogen-fluorine bond is particularly strong. Because it is difficult to break the bond between the hydrogen and the fluorine, the addition of HF is bound to be slow.

This applies to unsymmetrical alkenes as well as to symmetrical ones. For simplicity the examples given below are all symmetrical ones- but they don't have to be. Reaction rates increase as the alkene gets more complicated - in the sense of the number of alkyl groups (such as methyl groups) attached to the carbon atoms at either end of the double bond. For example:

There are two ways of looking at the reasons for this - both of which need you to know about the mechanism for the reactions.

Alkenes react because the electrons in the $$pi$$ bond attract things with any degree of positive charge. Anything which increases the electron density around the double bond will help this. Alkyl groups have a tendency to "push" electrons away from themselves towards the double bond. The more alkyl groups you have, the more negative the area around the double bonds becomes. The more negatively charged that region becomes, the more it will attract molecules like hydrogen chloride.

The more important reason, though, lies in the stability of the intermediate ion formed during the reaction. The three examples given above produce these carbocations (carbonium ions) at the half-way stage of the reaction:

The stability of the intermediate ions governs the activation energy for the reaction. As you go towards the more complicated alkenes, the activation energy for the reaction falls. That means that the reactions become faster.

In terms of reaction conditions and the factors affecting the rates of the reaction, there is no difference whatsoever between these alkenes and the symmetrical ones described above. The problem comes with the orientation of the addition - in other words, which way around the hydrogen and the halogen add across the double bond.

If HCl adds to an unsymmetrical alkene like propene, there are two possible ways it could add. However, in practice, there is only one major product.

This is in line with Markovnikov's Rule

Markovnikov's Rule

When a compound HX is added to an unsymmetrical alkene, the hydrogen becomes attached to the carbon with the most hydrogens attached to it already.

In this case, the hydrogen becomes attached to the CH2 group, because the CH2 group has more hydrogens than the CH group. Notice that only the hydrogens directly attached to the carbon atoms at either end of the double bond count. The ones in the CH3 group are totally irrelevant.

## A special problem with hydrogen bromide

Unlike the other hydrogen halides, hydrogen bromide can add to a carbon-carbon double bond either way around - depending on the conditions of the reaction. If the hydrogen bromide and alkene are entirely pure, then the hydrogen bromide adds on according to Markovnikov's Rule. For example, with propene you would get 2-bromopropane.

That is exactly the same as the way the other hydrogen halides add.

## If the hydrogen bromide and alkene contain traces of organic peroxides

Oxygen from the air tends to react slowly with alkenes to produce some organic peroxides, and so you do not necessarily have to add them separately. This is therefore the reaction that you will tend to get unless you take care to exclude all air from the system. In this case, the addition is the other way around, and you get 1-bromopropane:

This is sometimes described as an anti-Markovnikov addition or as the peroxide effect. Organic peroxides are excellent sources of free radicals. In the presence of these, the hydrogen bromide reacts with alkenes using a different (faster) mechanism. For various reasons, this doesn't happen with the other hydrogen halides. This reaction can also happen in this way in the presence of ultra-violet light of the right wavelength to break the hydrogen-bromine bond into hydrogen and bromine free radicals.

## Contributors

Electrophilic Addition of Hydrogen Halides II is shared under a not declared license and was authored, remixed, and/or curated by Jim Clark.