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Benzene is generally more reactive than ethane due to its unique structure and the presence of a conjugated π-electron system. While ethane is a saturated hydrocarbon that primarily undergoes reactions such as combustion and substitution, benzene can participate in electrophilic aromatic substitution reactions due to its delocalized electrons. This makes benzene more susceptible to reactions with electrophiles. However, benzene's stability also means it is less reactive in some conditions compared to alkenes or alkynes.
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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.
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.
Alkyl benzene can be easily oxidized as compared to benzenewhy?
Alkyl benzene can be more easily oxidized than benzene due to the presence of the alkyl group, which is more reactive than the aromatic ring. The alkyl substituent can donate electrons, enhancing the electrophilic character of the benzene ring and making it more susceptible to oxidation reactions. Additionally, the oxidation of the alkyl group can lead to the formation of more reactive species, further facilitating the overall oxidation process. In contrast, benzene's stable aromatic structure resists oxidation.
Which is the most reactive of the halogens and why is it the most reactive of the halogens?
fluorine is the most reactive
Why ethane is an important industrial chemical?
Ethane applications are: - precursor in ethylene preparation (the most important use) - refrigerant - fuel
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.
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.
Which is more reactive c2h4 or c2h6?
Ethylene (C2H4) is more reactive than ethane (C2H6) due to the presence of a pi bond in ethylene. The pi bond makes ethylene more susceptible to addition reactions with other molecules, while ethane lacks this double bond and is comparatively less reactive.
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.
Is this covalent compound soluble in water C2 H6?
C2H6 is the hydrocarbon ethane, and it has very low solubility in water. Most hyrdocarbons are like this. They're non-polar and so can't associate with the highly polar ends of the H20 molecules. Ethane would be soluble in a non-polar solvent such as benzene (C6H6).
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.
Alkyl benzene can be easily oxidized as compared to benzenewhy?
Alkyl benzene can be more easily oxidized than benzene due to the presence of the alkyl group, which is more reactive than the aromatic ring. The alkyl substituent can donate electrons, enhancing the electrophilic character of the benzene ring and making it more susceptible to oxidation reactions. Additionally, the oxidation of the alkyl group can lead to the formation of more reactive species, further facilitating the overall oxidation process. In contrast, benzene's stable aromatic structure resists oxidation.
