Benzene has a stable structure. Aspirin has an carboxylic group with delocalized electrons. So aspirin is more reactive than benzene.
pyrrole is more reactive towards electrophillic aromatic substiotution because it is able to stabilize the +ve charge of the intermediate carbocation
organic: methane, ethane, benzene, toluene inorganic: sodium chloride, dioxygen, magnesium oxide, potassium chloride
fluorine is the most reactive
BHC (Benzene Hexa Chloride) and DDT (Dichloro Diphenyl Trichloro ethane) are organic pesticides. Both are having detrimental effect on humans, particularly damage the reproductive system.
Ethyne is most reactive where as ethane is least.
Benzene has a stable structure. Aspirin has an carboxylic group with delocalized electrons. So aspirin is more reactive than benzene.
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.
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.
pyridine is less reactive than benzene because when we form its conjugate base then it'll b more stable than dat of benzene.. so more stabler means less reactive.......and also due to more resonance in benzene it will b more reactive...same 4 furan and pyrrole
Examples of organic compounds: ethane, stearic acid, galactose, resorcine, benzene, formaldehyde.
Yes, the dark stops the formation of a bromine radical
Yes. sure it will. generally covalent bond are formed and a wide range of fluoro derivatives if hydrocarbons are known. For example, fluoro methane, fluoro ethane, difluoro ethane, fluoro benzene, etc)
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).
pyrrole is more reactive towards electrophillic aromatic substiotution because it is able to stabilize the +ve charge of the intermediate carbocation
organic: methane, ethane, benzene, toluene inorganic: sodium chloride, dioxygen, magnesium oxide, potassium chloride
fluorine is the most reactive