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Benzene
Formula C6H6 unsaturated

Original slide
prepared for the
Benzene
• Its molecular formula, C6H6 , was established in 1834,
after the compound's discovery by Faraday.
• The formula of benzene (C6H6) caused a mystery for
many years after its discovery, as no explanation had
been found that could account for all the bonds —
carbon usually forms four single bonds and hydrogen
one.
• The chemist Friedrich August Kekulé was the
first to deduce the ring structure of benzene (1865).
• The cyclic nature of benzene was confirmed by the
crystallographer Kathleen Lonsdale.
•

Original slide
prepared for the
Benzene

• Using X-ray diffraction, researchers discovered that all
of the carbon-carbon bonds in benzene are of the same
length, and it is known that a single bond is longer than
a double bond.
• In addition, the bond length, the distance between the
two bonded atoms in benzene is greater than a double
bond, but shorter than a single bond.
• There seemed to be in effect, a bond and a half between
each carbon.

Original slide
prepared for the
Benzene
• Benzene is also a planar molecule (all the atoms lie
in one plane). Each carbon atom is bonded to its
neighbor with one electron from each atom. Since
each atom has two neighbors, this uses two electrons
from each atom.
• Another electron from each carbon is used to bond
the hydrogen attached to it.
• The remaining six electrons orbit the atomic nuclei at
right angles to the plane of the ring and also overlap
each other, consequently blurring their orbits both
above and below the ring ( 3 electrons in upper ring
and 3 electrons in down ring).
Original slide
prepared for the
Benzene
• As a result, the electrons are shared equally
between the carbon atoms and exist as two clouds,
one above and one below the plane of the carbon
ring.
• Since these latter six electrons are not confined to
specific carbon atoms, they are said to be
delocalised.
• This is usually represented in structural formula as
a hexagon with a circle in the centre to represent
the shared nature of the electrons
Original slide
prepared for the
Bonding in benzene

H

H
C
H

C
C

C
C
H

6 electrons in a
delocalised π bond

C

H

above and below
the plane of the
atoms

H

Original slide
prepared for the
Benzene

References
Steve Lewis for the Royal Society of Chemistry
Original slide
prepared for the

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7.2 bonding in benzene 7.2

  • 2. Benzene • Its molecular formula, C6H6 , was established in 1834, after the compound's discovery by Faraday. • The formula of benzene (C6H6) caused a mystery for many years after its discovery, as no explanation had been found that could account for all the bonds — carbon usually forms four single bonds and hydrogen one. • The chemist Friedrich August Kekulé was the first to deduce the ring structure of benzene (1865). • The cyclic nature of benzene was confirmed by the crystallographer Kathleen Lonsdale. • Original slide prepared for the
  • 3. Benzene • Using X-ray diffraction, researchers discovered that all of the carbon-carbon bonds in benzene are of the same length, and it is known that a single bond is longer than a double bond. • In addition, the bond length, the distance between the two bonded atoms in benzene is greater than a double bond, but shorter than a single bond. • There seemed to be in effect, a bond and a half between each carbon. Original slide prepared for the
  • 4. Benzene • Benzene is also a planar molecule (all the atoms lie in one plane). Each carbon atom is bonded to its neighbor with one electron from each atom. Since each atom has two neighbors, this uses two electrons from each atom. • Another electron from each carbon is used to bond the hydrogen attached to it. • The remaining six electrons orbit the atomic nuclei at right angles to the plane of the ring and also overlap each other, consequently blurring their orbits both above and below the ring ( 3 electrons in upper ring and 3 electrons in down ring). Original slide prepared for the
  • 5. Benzene • As a result, the electrons are shared equally between the carbon atoms and exist as two clouds, one above and one below the plane of the carbon ring. • Since these latter six electrons are not confined to specific carbon atoms, they are said to be delocalised. • This is usually represented in structural formula as a hexagon with a circle in the centre to represent the shared nature of the electrons Original slide prepared for the
  • 6. Bonding in benzene H H C H C C C C H 6 electrons in a delocalised π bond C H above and below the plane of the atoms H Original slide prepared for the
  • 7. Benzene References Steve Lewis for the Royal Society of Chemistry Original slide prepared for the