In reality, benzene does not contain alternating single and double bonds. It is more accurate to say that each carbon-carbon bond is in an intermediate state between a single and a double bond. Benzene therefore displays a property known as resonance.
As the molecular formula for benzene is C6H6 so acetylene CH Triple Bond CH should be its monomer.
6 C-H bonds 3 C-C bonds 3 C=C bonds (note: the carbon -carbon bonds are resonating and thus each C-C bond has bond order 1.5 )
Benzene has covalent bonds. Each of the six carbons in benzene is sp2 hybridized meaning the ring has both sigma bonds and pi bonds. Benzene is aromatic meaning its pi electrons are delocalized and form a pi system.
benzene and water are immiscible liquids. therefore they have to be separated by means of a separating funnel.
There are three deactivating -NO2 groups attached to benzene ring.They reduce electron density of benzene ring very much.So electrons of Oxgen in -OH group attract to benzene ring.Then the negativity of Oxygen reduces.So it is very much easy to break O-H bond and emmit H+.
1.5
In reality, benzene does not contain alternating single and double bonds. It is more accurate to say that each carbon-carbon bond is in an intermediate state between a single and a double bond. Benzene therefore displays a property known as resonance.
If you could add a pair of hydrogen ions to any double bond of the benzene ring it would not be benzene anymore, on the one hand.
c-c bond length in benzene is 1.397 angston and that of ethene is 1.34 angston structure of benzene is a resonance hybrid, therefore all the c-c bond lengths are equal but different from those in alkanes,alkenes, and alkynes.
As the molecular formula for benzene is C6H6 so acetylene CH Triple Bond CH should be its monomer.
6 C-H bonds 3 C-C bonds 3 C=C bonds (note: the carbon -carbon bonds are resonating and thus each C-C bond has bond order 1.5 )
The two resonance configuration is equally probable in benzene. i.e. all the c-c bonds have 50% probability of single bond and double bond. As a result all the bonds become equal.
No. O-H bond energy is larger
Benzene has covalent bonds. Each of the six carbons in benzene is sp2 hybridized meaning the ring has both sigma bonds and pi bonds. Benzene is aromatic meaning its pi electrons are delocalized and form a pi system.
benzene and water are immiscible liquids. therefore they have to be separated by means of a separating funnel.
Benzene has the structure C6H6 so should have double bonds but it does not instead it has a unsaturated electron above or below it. This is also known as an area of high electron density.