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substitution reaction. This is because the halogen atom attached to benzene ring in haloarenes
is slightly deactivating and ortho
and para directing. so attack can only take place at ortho
and para. Also the halogen atom in Haloarenesdue to its -I effect has some tendancy
to withdraw electrons from the benzene ring and hence making it deactivating.
Since the ring gets deactivated as compared to benzene, haloarenes
are less reactive than benzene in electrophillic
substituion
reaction.
What else can I help you with?
What Aromatic Hydrocarbon has been prepared in the reaction between Sulfuric Acid and Benzene?
Benzene sulfonic acid is produced in the reaction between sulfuric acid and benzene. This reaction involves the substitution of a hydrogen atom on the benzene ring with a sulfonic acid group (SO3H).
Why haloaranes are much less reactive than haloalkanes towards nuclophillic substitution rxn?
Haloarenes are less reactive than haloalkanes towards nucleophilic substitution reactions because the aromaticity of the benzene ring in haloarenes provides extra stability to the molecule. This stability reduces the likelihood of breaking the aromaticity of the ring during the substitution reaction. In contrast, haloalkanes do not possess this extra stabilization, making them more prone to undergo nucleophilic substitution reactions.
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.
What happens when benzene reacts with chlorine in bright sunlight?
When benzene reacts with chlorine in bright sunlight, substitution reactions can occur where one or more hydrogen atoms in the benzene ring are replaced by chlorine atoms, forming chlorobenzene derivatives. This process is known as chlorination and is a type of electrophilic aromatic substitution reaction.
What happens when benzene is treated with a mixture of concentrated sulphuric acid and nitric acid?
Benzene reacts with a mixture of concentrated sulfuric acid and nitric acid to undergo nitration, resulting in the substitution of one or more hydrogen atoms with nitro groups (-NO2) on the benzene ring. This reaction forms nitrobenzene as the primary product.
Why halobenzenes are less reactive towards nucleophilic substitution reaction?
i think the question is wrong.benzene doesn't respond nucleophilic substitution respond electrophilic substitution it is electrophilic then due to resonance there is a partial double bond between carbon of benzene and halogens.so halobenzenes are chemically inert towards electrophilic substitution.
What Aromatic Hydrocarbon has been prepared in the reaction between Sulfuric Acid and Benzene?
Benzene sulfonic acid is produced in the reaction between sulfuric acid and benzene. This reaction involves the substitution of a hydrogen atom on the benzene ring with a sulfonic acid group (SO3H).
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.
Where you get Maharastra SET question paper?
Benzene undergo substitution reaction rather than addition?
Why haloaranes are much less reactive than haloalkanes towards nuclophillic substitution rxn?
Haloarenes are less reactive than haloalkanes towards nucleophilic substitution reactions because the aromaticity of the benzene ring in haloarenes provides extra stability to the molecule. This stability reduces the likelihood of breaking the aromaticity of the ring during the substitution reaction. In contrast, haloalkanes do not possess this extra stabilization, making them more prone to undergo nucleophilic substitution reactions.
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.
What purpose does FeCl3 serve in the electrophilic aromatic substitution reaction between chlorine and benzene?
FeCl3 acts as a Lewis acid catalyst in the reaction, activating the chlorine molecule by coordinating with it and facilitating its electrophilic attack on the aromatic ring of benzene. This activation process increases the electrophilicity of the chlorine, making it more reactive towards aromatic substitution.
Chemical reaction between phenol and bromine water?
The reaction between phenol and bromine water results in the substitution of a hydrogen atom on the benzene ring with a bromine atom. This forms bromophenol as the product. The reaction is a bromination reaction and the presence of phenol's hydroxyl group activates the benzene ring towards electrophilic substitution.
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 benzene undergoes electrophilic substitution reaction whereas alkenes undergoes addition reaction?
The cation formed upon addition of an electrophile to benzene is highly stabilized by resonance,whereas the cation formed to an alkene is stabilized by hyperconjugation. The loss of a proton in benzene is favourable due to the restoration of the cyclic pi-system.
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 benzene undergo electrophilic substitution reaction easily and nucleophilic substution reaction with difficulty easily and?
the electron in benzene are delocalised making d ring to be elctron rich,thereby undergoing electrophilic substitution.benzene cannot undergo nucleophillic substitution,it can only undergo if it is substituted with an electron withdrawing group
