Methane + Cl2 ---> Ch3Cl + alcoholic KOH ---> Ethene + Br-Br ---> vicinal dihalide with the double bond being replaced by to C-Br bonds. + alcoholic KOH ---> CH2(double bond)CHBr + NaNH2 ---> Ethyne . Pass ethyne through a red hot iron tube and you will get benzene.
Benzene is formed as the result of chemical reactions. When a chain of six carbon atoms does like a dog biting its tail and forms a circle this becomes the benzene ring. C6-H12 I expect. The 6 carbon benzene ring contains 3 C-C single bonds and 3 C=C double bonds - with no side chains. Add 3 nitros as side chains and we get dynamite.
There are many ways to form benzene derivatives..
For e.g, haloarenes are formed by electrophilic aromatic substitution,diazotisation rxs,
Sandmeyer rxns..
Proximity and valence electrons
Ask Dave Dash
Carbon and hydrogen. Benzene is a hexagonal ring formed of carbon-carbon bonds, alternatively double and single. http://i205.photobucket.com/albums/bb157/hortaux/benzene.jpg
C6H3Cl3 The benzene ring has 6 carbon atoms, each of which is given a number and this continues in a clockwise direction. Chlorine atoms are attached to carbons 1, 2 and 4.
A five sided shape of the hexagon is used to represent and model a molecule of benzene. The hexagon will have alternating double lines (or a single double) to indicate the presence of its characteristic double (sp2) bond.
A benzo is a divalent radical formed by the removal of two adjacent hydrogen atoms from a benzene ring.
6-carbon ring
The density of benzene is 876.50 kg/m to the third. Benzene is composed of six carbon atoms that are joined in a ring shape with a single hydrogen atom attached to each of those carbon atoms.
Benzene is an organic molecule made up of six carbon atoms connected to form a ring. This is called the benzene ring. The benzene ring structure occures in several other, more complex, organic moleculed.
Benzene has 42 electrons. With chemical formula C6H6: 6 electrons for each carbon 1 electron for each hydrogen... 6(6) + 1(6) = 36 + 6 = 42 electrons Each carbon has 3 'sp2' orbitals: -one of which overlaps the 's' orbital of H -and the remaining 'sp2' orbitals constitute the sigma bonds between carbons Each carbon has a 'p' orbital (each contain a single electron) which create two rings of electron density above and below the benzene ring. These 6 adjacent 'p' orbitals fully conjugate the ring, resulting in benzene's aromaticity and unusual stability.
Benzene is a covalent compound. It is formed of 6 Carbon atoms and 6 Hydrogen atoms which all share electrons in covalent bonds. A ring of delocalised electrons sit above and below the plane of the carbon atoms making Benzene stable and relatively unreactive.
The organic compound, hydroquinone, is a phenol with formula C6H4(OH)2. Consequently, it's chemical structure is formed from atoms of the elements carbon, hydrogen and oxygen. The atoms are typically arranged to form a benzene ring and two hydroxyl groups bonded to the ring.
Benzene is equal parts hydrogen and carbon, and has C6H6 as it molecular formula. It is actually a ring with the carbons in the middle and the hydrogen bonded one-to-one with the carbon atoms on the outside. Use the link below for more information and to see a "picture" that cannot be drawn here.
Benzaldehyde has the formula C7H6O, it has the carbonyl carbon of the aldehyde bound to a benzene ring. You can't have a =O unit bound directly to the benzene ring because you would have a carbon with five bonds.
Benzene molecule is planar in nature. This is because like all carbons, it contains two spxpy hybrid carbon that form a hexagonal ring.
Meso-stilbene dibromide is an organic molecule. Its structure is a benzene ring bonded to a carbon with a hydrogen and a bromine. That carbon is bonded to another carbon with a bromine that is ANTI to the first bromine. This carbon is then also bonded to a benzene ring.
Ask Dave Dash
Benzene is an aromatic organic molecule. Its formula is C6H6. The carbons are joined in a ring that is represented as a flat hexagon. The associated hydrogen atoms are represented as being attached to the individual carbon atoms but the electrons for sp2 bonding with the C-C bonding of the benzene molecule are actually distributed equally between each of the six carbon atoms - a phenomena referred to as electron delocalization or a superposition of so-called resonance structures. The delocalization contributes to benzene's thermodynamic stability and that of related aromatic compounds.