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An alkene is more reactive than alkyne. as double bond can donate pair of electron. while in tripple bond the bond length is less than double bond. Alkkynes have more attractive forces than alkene. so alkene is more reactive.

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Is benzene reactive with bromine in the dark?

No, benzene is not reactive with bromine in the dark because the aromatic nature of benzene stabilizes its electron configuration. Without light or a catalyst, the reaction between benzene and bromine is not energetically favored.


Why chlorine makes benzene less reactive?

This is because chlorine is an electronegative group and is pulling electrons away from benzene. This makes the ring less reactive and more positive. Then when a positive electrophile tries to attach, the benzene does not want to react.


Why does bromine react with hexene but not benzene?

Adding halogens to alkene groups (X2) requires that the product adopt an anti configuration. Hexene will also lose its double bond upon bromination. Benzene is energetically unfavorable when a reaction attempts to break its double bond. The resonance benzene has makes it very stable, and thus very hard to break.


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.


Is phenol easier or more difficult to substitute with bromine than benzene?

The substitution reactions of phenol are easier than benzene, phenol directly reacts with bromine and gives tribromo phenol while benzene requires FeCl3 as a catalyst and gives mono bromo phenol.

Related Questions

What compound is most reactive?

ethyne


Which of the following is most reactive A. ethane B. ethene C. ethyne D. they are all equally reactive?

Ethyne is most reactive where as ethane is least.


How is benzene prepared from ethyne?

Benzene can be prepared from ethyne through a process called electrophilic aromatic substitution. In this process, ethyne reacts with a strong acid catalyst such as concentrated sulfuric acid to form benzene. The high temperature required for this reaction causes the triple bond in ethyne to break and the resulting carbons bond to form a 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.


Is benzene reactive with bromine in the dark?

No, benzene is not reactive with bromine in the dark because the aromatic nature of benzene stabilizes its electron configuration. Without light or a catalyst, the reaction between benzene and bromine is not energetically favored.


Why chlorine makes benzene less reactive?

This is because chlorine is an electronegative group and is pulling electrons away from benzene. This makes the ring less reactive and more positive. Then when a positive electrophile tries to attach, the benzene does not want to react.


Is benzene less reactive towards electrophillic substitution reaction?

No, Haloarenes are less reactive than benzene towards electrophillic substitution reaction. This is because the halogen atom attached to benzene ring in haloarenesis slightly deactivating and orthoand para directing. so attack can only take place at orthoand para. Also the halogen atom in Haloarenesdue to its -I effect has some tendancyto withdraw electrons from the benzene ring and hence making it deactivating.Since the ring gets deactivated as compared to benzene, haloarenesare less reactive than benzene in electrophillicsubstituionreaction.


Why the benzene ring is not much reactive as the pyrrole?

The benzene ring is less reactive than pyrrole because it is very stable due to its aromaticity. The delocalization of pi electrons in the benzene ring creates a high resonance energy, making it less inclined to undergo reactions. In contrast, pyrrole is more reactive because it is not fully aromatic and has more reactive sites available for bonding.


Why benzene is less reactive than alkene?

Benzene is less reactive than alkenes because it has a stable aromatic ring structure, which leads to a high degree of resonance stabilization. This stability reduces the tendency of benzene to undergo addition reactions that are commonly seen with alkenes. Additionally, the delocalization of electrons in the benzene ring provides extra stability, making it less likely to undergo reactions that would disrupt this resonance.


Why haloarenes are less reactive towards electrophile than benzene?

Haloarenes are less reactive towards electrophiles than benzene because the halogen substituents on the aromatic ring act as electron-withdrawing groups, reducing the electron density on the ring and making it less susceptible to attack by electrophiles. This results in a decreased reactivity towards electrophilic substitution reactions compared to benzene.


Why nitration of nitrobenzene is difficult than nitration of benzene?

Nitration of nitrobenzene is more difficult because the nitro group is an electron-withdrawing group, making the nitrobenzene less reactive towards electrophilic aromatic substitution reactions. In contrast, benzene is more reactive because it does not have any electron-withdrawing groups attached to it.


What are the key differences between phenol and benzene in terms of their chemical properties and reactivity?

Phenol and benzene are both aromatic compounds, but phenol has a hydroxyl group (-OH) attached to the benzene ring, making it more reactive than benzene. Phenol can undergo reactions such as oxidation and substitution more readily than benzene. Additionally, phenol is more acidic than benzene due to the presence of the hydroxyl group.