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Is a benzene ring stable

Updated: 8/9/2023
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11y ago

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Benzene has the structure C6H6 so should have double bonds but it does not instead it has a unsaturated electron above or below it. This is also known as an area of high electron density.

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14y ago
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14y ago

because the structure of benzene, which is a ring, makes it so stable. each bond is of the same length and the pi bond is partial pi bond, as 1 lobe can be shared between neighbouring atoms.

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13y ago

Benzene has no reactive agents except hydrogen.

I don't have the chemical formula for PYRan but we can see that it related to PYRotechnics which are quite unstable.

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11y ago

yes a benzene ring is stable.

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10y ago

Stable

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Q: Is a benzene ring stable
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Related questions

Why is benzene stable to towards KMnO4 oxidation?

Benzene is stable towards oxidation of KMnO4 because it is a stable aromatic molecule. For an oxidation there would have to be a reaction, but since there is no reaction it is stable. Benzene is stable until there is a catalyst such as FeCl3, FeBr3, AlCl3, etc. This type of catalyst is used because it makes the bonding molecule more electrophilic and so it wants to attach to the electron-rich, also know as nucleophilic, benzene ring.


Benzene ring has three pi-bonds in it but is still quite stable.explain?

Benzene has a property called resonance. Because of this, the three pi-bonds in benzene act as a rather delocalized single pi-structure. So, benzene does not actually have 3 distinct pi-bonds. This pi-structure is stable, which explains why benzene is more stable than it would be if it had 3 pi-bonds.


Why aromatic compound undergoes electrophilic substitution?

in aromatic amines due to the presence of of the amine group, the conjugation of the benzene ring proceeds through making the ring more stable.


Why nitration of toluene is easier than benzene?

Hi ,As you know from the structures of both the compounds that toluene has a methyl group on the benzene ring which is electron releasing group and hence activate the benzene ring by pushing the elctrons on the benzene ring. On the other hand nitro group on the benzene ring is electron withdrawing group which deactivates the benzene ring by withdrawing the electrons from the benzene ring . Now in the nitration attack of the nucleophile ( NO2 +) takes place. Hence reaction will takes place on that benzene faster which have more electron density on its ring which is the case of toluene.


What does a ring do for chemistry?

A ring is a cyclic molecule as benzene.


Why is benzene classified as an aromatic compound?

There isn't such a thing as more aromatic. Something is aromatic or not. If you are referring to the stabilization due to aromaticity, naphthalene has more electrons in the stabilizing Pi-system is therefore more stabilized.


How many resonance structure benzene have?

There are 2 resonance structures for benzene.


What is relationship among benzene Toluene and Xylene?

They are all homologues that contain a benzene ring


Compound that contains a benzene ring?

Benzene is an organic molecule made up of six carbon atoms connected to form a ring. This is called the benzene ring. The benzene ring structure occures in several other, more complex, organic moleculed.


Molecular shape of C6H6?

benzene ring


Why is aspirin more reactive than benzene?

Benzene has a stable structure. Aspirin has an carboxylic group with delocalized electrons. So aspirin is more reactive than benzene.


What role does benzene ring play in bonding?

Catalyst