mechanism for the hydration of ethene - A-Level Chemistry Revision - XtremePapers

THE MECHANISM FOR THE ACID CATALYSED HYDRATION OF ETHENE

This page describes the mechanism for the hydration of ethene to make ethanol using phosphoric(V) acid as the catalyst.

The hydration of ethene to make ethanol

A reminder of the facts

Ethene is mixed with steam and passed over a catalyst consisting of solid silicon dioxide coated with phosphoric(V) acid. The temperature used is 300°C and the pressure is about 60 to 70 atmospheres.

Note: If you are interested in the reasons for the conditions used in this reaction, you will find them in the equilibrium section of this site by following this link.

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The mechanism for the hydration of ethene

This assumes that you know about the electrophilic addition reactions of ethene, and about the use of curly arrows in organic reaction mechanisms. If you aren't happy about either of these follow the link below before you go any further.

Note: Follow this link for the electrophilic addition reactions of ethene. You will find a link explaining the use of curly arrows in mechanisms on that page if you need it.

These pages are in a completely different part of the site. The quickest way to return here is to use the BACK button on your browser, or the history file or the Go menu if you get seriously waylaid!

All the steps in the mechanism below are shown as one-way reactions because it makes the mechanism look less confusing. It doesn't affect the argument, but in fact all the steps are reversible.

Step 1

All of the hydrogen atoms in the phosphoric(V) acid are fairly positively charged because they are attached to a very electronegative oxygen atom.

Note: If you aren't sure about electronegativity, you might like to follow this link.

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One of these hydrogens is strongly attracted to the carbon-carbon double bond. The pi part of the bond breaks and the electrons in it move down to make a new bond with the hydrogen atom. That forces the electrons in the hydrogen-oxygen bond down entirely onto the oxygen.

Note: It is easy to see why the oxygen carries a negative charge. It has gained full control over the electron pair in the original bond - so has acquired an extra electron which originally belonged to the hydrogen.

The carbon atom has a positive charge because one of the electrons in the pi bond originally belonged to it. It loses that electron when the pi bond breaks.

Step 2

The carbocation (carbonium ion) formed reacts with one of the lone pairs on a water molecule. A carbocation is one which carries a positive charge on a carbon atom.

Note: The easiest way of remembering that the oxygen has to carry a positive charge is that you are reacting a positive ion with a neutral molecule. That means that there must be a positive charge on the product somewhere.

The only way that an oxygen atom can be joined to three things at the same time is if it carries a positive charge. A positive charge gives the oxygen the same electronic structure as a nitrogen atom which can, of course, form three bonds.

Step 3

Finally, one of the hydrogens on the oxygen is removed by reaction with the dihydrogenphosphate(V) ion, H₂PO₄^-, formed in the first step.

The phosphoric(V) acid catalyst has been regenerated.

Note: This is a bit of a simplification. The concentrated phosphoric(V) acid probably contains some water, in addition to the water in the steam. It is likely that some of the hydrogen ions in this last step will be removed by water molecules, and possibly transferred to a dihydrogenphosphate(V) ion to make phosphoric(V) acid in a later step. Other hydrogen ions will be removed directly by the dihydrogenphosphate(V) ions as shown above. Don't worry about this. Your examiners will almost certainly not be looking for this sort of fine detail.

The reversibility of this reaction

As mentioned before, this reaction is entirely reversible - and so each step is reversible. In the reverse direction, this is a dehydration of ethanol to make ethene. If you are interested, you will find the mechanism written in the reverse direction on another page.

Note: This link will lead you to the reverse of this hydration process, the dehydration of ethanol.

The catalyst used on that page is concentrated sulphuric acid rather than phosphoric(V) acid, because that is the acid often used in the lab. You could write either of these mechanisms (in either direction) perfectly well using the structure of either of these acids.

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