Just A Moment - Ring Reactions Of Phenol

This page looks at the way the reactions of the benzene ring in phenol are modified by the presence of the attached -OH group. It covers the reactions of phenol with bromine water và with nitric acid.

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How does the -OH group modify the ring reactions?

Activation of the ring

The -OH group attached to lớn the benzene ring in phenol has the effect of making the ring much more reactive than it would otherwise be.

For example, as you will find below, phenol will react with a solution of bromine in water (bromine water) in the cold and in the absence of any catalyst. It also reacts with dilute nitric acid, whereas benzene itself needs a nitrating mixture of concentrated nitric acid & concentrated sulphuric acid.

Warning! You need khổng lồ understand about the bonding in benzene in order to make sense of this next bit.

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One of the lone pairs on the oxygen atom in the -OH group overlaps with the delocalised ring electron system . . .

. . . Giving a structure rather lượt thích this:

The donation of the oxygen"s lone pair into the ring system increases the electron density around the ring.

A benzene ring undergoes substitution reactions in which the ring electrons are attacked by positive ions or the slightly positive parts of molecules. In other words, it undergoes electrophilic substitution. If you increase the electron density around the ring, it becomes even more attractive to lớn incoming electrophiles. That"s what happens in phenol.

Note: If you aren"t sure what any of these terms mean, you could find out by following this link to a page introducing electrophilic substitution.

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The directing effect of the -OH group

The -OH group has more activating effect on some positions around the ring than others (for reasons which go beyond UK A level). That means that incoming groups will go into some positions much faster than they will into others.

The net effect of this is that the -OH group has a 2,4-directing effect. That means that incoming groups will tend lớn go into the 2- position (next door to lớn the -OH group) or the 4- position (opposite the -OH group). You will get hardly any of the 3- isomer formed - it is produced too slowly.

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Specific examples

Reaction with bromine water

If bromine water is added lớn a solution of phenol in water, the bromine water is decolourised & a white precipitate is formed which smells of antiseptic.

The precipitate is 2,4,6-tribromophenol.

Notice the multiple substitution around the ring - into all the activated positions. (The 6- position is, of course, just the same as the 2- position. Both are next door lớn the -OH group.)

Note: Bromine water is normally used as a demo for a C=C double bond. The important difference with phenol is the formation of a white precipitate as well as the bromine water being decolourised.

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Reactions with nitric acid

The reactions with nitric acid are complicated because nitric acid is an oxidising agent, and phenol is very easily oxidised lớn give complex tarry products. What follows misses all that complication out, & just concentrates on the ring substitution which happens as well.

With dilute nitric acid

Phenol reacts with dilute nitric acid at room temperature khổng lồ give a mixture of 2-nitrophenol & 4-nitrophenol.

With concentrated nitric acid

With concentrated nitric acid, more nitro groups substitute around the ring to lớn give 2,4,6-trinitrophenol (old name: picric acid).

Questions to kiểm tra your understanding

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Activation of the ring

The -OH group attached to lớn the benzene ring in phenol has the effect of making the ring much more reactive than it would otherwise be. For example, as you will find below, phenol will react with a solution of bromine in water (bromine water) in the cold & in the absence of any catalyst. It also reacts with dilute nitric acid, whereas benzene itself needs a nitrating mixture of concentrated nitric acid và concentrated sulfuric acid.

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Notice the multiple substitution around the ring - into all the activated positions. (The 6- position is, of course, just the same as the 2- position. Both are next door to the -OH group.)

Example 2: Reactions with Nitric Acid

The reactions with nitric acid are complicated because nitric acid is an oxidizing agent, & phenol is very easily oxidized khổng lồ give complex tarry products. What follows misses all that complication out, và just concentrates on the ring substitution which happens as well.

With dilute nitric acid: Phenol reacts with dilute nitric acid at room temperature lớn give a mixture of 2-nitrophenol và 4-nitrophenol.