Electrophilic reagents are chemical species which in the course of chemical reactions, acquire electrons or a share in electrons from other molecules or ions. Nucleophilic reagents do the opposite of electrophilic reagents.
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.
Yes, they strongly resemble soot.
A carbon nanotube can be compared to the fullerenes, a group of spherical carbon allotropes (allotropes are different forms of a single element).The key difference is that the fullerenes are spherical in shape whereas carbon nanotubes resemble a fullerene network that has been stretched into a cylindrical shape. Furthermore, nanotubes contain more carbon atoms than most fullerenes do.
jaom maran
The Electrophilic Addition Reaction is when the attacking species during the addition reaction is"Electrophile", it is called "electrophilic addition reaction". Examine: (+) (-) (+) (-) (+) (-) CH2Br-CH2BràH2C-CH2+BrBr-àH2C=CH2+Br2-
Electrophilic reagents are chemical species which in the course of chemical reactions, acquire electrons or a share in electrons from other molecules or ions. Nucleophilic reagents do the opposite of electrophilic reagents.
Fullerenes are named after William Buckminster Fuller, a designer and philosopher who theorized their existence and uses.
Fullerenes are prepared by vaporizing graphite rod in helium atmosphere. A mixture of fullerenes like C60, C70 etc are formed which are separated by solvent extraction method.C60 is obtained by column chromatography using alumina as the adsorbent and hexane as the solvent.
phophite attacks the electrophilic carbon, the oxyanion attacks the another electrophilic carbon and its anion will be cyclised with phosponiumion.
what is the structure of Buckminster fullerene
No it is not electrophilic.It is a nucleophile
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.
Some examples of fullerenes include buckminsterfullerene (C60), which is a soccer ball-shaped molecule composed of 60 carbon atoms, and carbon nanotubes, which are cylindrical fullerenes. Another example is the fullerene derivative known as C70, which consists of 70 carbon atoms arranged in a spherical structure.
Today fullerenes are not usually used compounds.
All forms of carbon.
electrophilic attack