Ethane
Conformation of Ethane
• When an ethane molecule rotates about it's carbon-
carbon single bond two extreme conformations can
be result, the staggered and eclipsed conformation.
• Here we will use Newman projection to discuss the
confirmation.
H
H
H
H H
H
H H
H
HH
H
60°
0°
Staggered Eclipsed
Rotation around bond
• If one of the methyl group is allowed to rotate
keeping the rest of molecule undisturbed and
number of possible arrangement can be
obtained.
60° 120°
360° 300°
240°
180°
H
HH
H
H
H
HH
H
H
H
H
H
H
H
HH
H
H
H H
H
H
H
H
H
HH
H
H
H
H
H
H H
H
H
H
H H
H
H
(I)- Eclipsed
Repulsion more
Energy more
Less stable
(II) - Staggered
Repulsion less
Energy less
More stable
(III)-Eclipsed
Repulsion more
Energy more
Less stable
(VI)-Staggered
Repulsion less
Energy less
More stable
(V)-Eclipsed
Repulsion more
Energy more
Less stable
(VII)-Eclipsed
Repulsion more
Energy more
Less stable
(IV)-Staggered
Repulsion less
Energy less
More stable
Energy level
• By doing so six possible confirmation can be
obtained out of which 3 are staggered (II,IV,VI)
and 3 are eclipsed form (I/VII,III,V).
• Potential energy of I,III,V,VII is greater than
that of II,IV,VI due to repulsive forces.
• Stability of II,IV,VI is greater than that of
I,III,V,VII.
I , III, V, VII > II , IV , VI
II, IV, VI > I , III , V , VII
Energy level diagram
n-Butane
CH3-CH2-CH3
C – C – C – C
H
H
HH
HH H
H
H
H
1 432
Kekule structure
Skeletal structure
condensed structure
Possible rotation for n-Butane
C – C – CH2-CH3
H
HH
HH
1 2
H3C – C – C – CH3
HH
H H
32
Rotation around C1 and C2
Rotation around C2 and C3
Structure I Structure II *
Conformations of n-Butane
• Butane has three carbon-carbon single bond
and molecule can rotate about each of them .
• If the rotation will be about C2 and C3 bond
then confirmation will be symmetrical.
• Different conformation of butane can be
obtained by rotating about its middle carbon-
carbon single bond.
60° 120°
360° 300°
240°
180°
H3C
H3CH3C
H3C
CH3
CH3
CH3CH3
CH3
H3C
CH3
CH3
H3C
CH3
H
HH
H
H
H H
H
H
H
H
H
HH
H
H
H
H
H
H H
H
H
H
H H
H
H
(I)-Fully Eclipsed
Very high Repulsion
Very high Energy
Least stable
(II) – Staggered(Gauche)
Moderate Repulsion
Moderate Energy
Moderately stable
(III)-Partly Eclipsed
Repulsion high
Energy high
Less stable
(IV)-Staggered (Anti)
Repulsion less
Energy less
More stable
(VII)-Fully Eclipsed
Very high Repulsion
Very high Energy
Least stable
(VI) – Staggered(Gauche)
Moderate Repulsion
Moderate Energy
Moderately stable
(V)-Partly Eclipsed
Repulsion high
Energy high
Less stable
Conformers of n-Butane
• Butane has 3 staggered (II,IV,VI) conformer.
• IV (Anti conformer), in which the two methyl
group are as far apart as possible is more
stable and require very less energy.
• II , VI (Gauche conformer)
• Butane has 3 eclipsed (I/VII,III,V)
• I and VII are fully eclipsed
• III and V are Partly eclipsed
Energy level
• Potential energy of I,VII is greater followed by
III,V and II,VI. Conformer IV require very less
energy because bulky group CH3 is far apart.
• Stability of IV is greater than that of II,VI
followed by III, V and I,VII.
I ,VII > III, V > II, VI > IV
IV > II, VI > III, V > I, VII
Energy level diagram
Conformation for n-Butane
C – C – CH2-CH3
H
HH
HH
1 2
Structure I
60° 120°
360°
300°
240°
180°
H3C
H3C
H3C
CH2-CH3
CH3
CH3
CH3
H3C-H2C
CH3
H
HH
H
H
H H
H
H
H
H
H
HH
H
H
H
H
H
H H
H
H
H
H H
H
H
CH2-CH3CH2-CH3
CH2-CH3
H3C-H2C
H3C-H2C
(I)- Eclipsed
Repulsion more
Energy more
Less stable
(II) - Staggered
Repulsion less
Energy less
More stable
(III)-Eclipsed
Repulsion more
Energy more
Less stable
(IV)-Staggered
Repulsion less
Energy less
More stable
(VI)-Staggered
Repulsion less
Energy less
More stable
(V)-Eclipsed
Repulsion more
Energy more
Less stable
(VII)-Eclipsed
Repulsion more
Energy more
Less stable
Energy level
• By doing so six possible confirmation can be
obtained out of which 3 are staggered (II,IV,VI)
and 3 are eclipsed form (I/VII,III,V).
• Potential energy of I,III,V,VII is greater than
that of II,IV,VI due to repulsive forces.
• Stability of II,IV,VI is greater than that of
I,III,V,VII.
I , III, V, VII > II , IV , VI
II, IV, VI > I , III , V , VII
Thank you my dear students...!!!

Conformation of ethane and n butane

  • 2.
  • 3.
    Conformation of Ethane •When an ethane molecule rotates about it's carbon- carbon single bond two extreme conformations can be result, the staggered and eclipsed conformation. • Here we will use Newman projection to discuss the confirmation. H H H H H H H H H HH H 60° 0° Staggered Eclipsed
  • 4.
    Rotation around bond •If one of the methyl group is allowed to rotate keeping the rest of molecule undisturbed and number of possible arrangement can be obtained.
  • 5.
    60° 120° 360° 300° 240° 180° H HH H H H HH H H H H H H H HH H H HH H H H H H HH H H H H H H H H H H H H H H (I)- Eclipsed Repulsion more Energy more Less stable (II) - Staggered Repulsion less Energy less More stable (III)-Eclipsed Repulsion more Energy more Less stable (VI)-Staggered Repulsion less Energy less More stable (V)-Eclipsed Repulsion more Energy more Less stable (VII)-Eclipsed Repulsion more Energy more Less stable (IV)-Staggered Repulsion less Energy less More stable
  • 6.
    Energy level • Bydoing so six possible confirmation can be obtained out of which 3 are staggered (II,IV,VI) and 3 are eclipsed form (I/VII,III,V). • Potential energy of I,III,V,VII is greater than that of II,IV,VI due to repulsive forces. • Stability of II,IV,VI is greater than that of I,III,V,VII. I , III, V, VII > II , IV , VI II, IV, VI > I , III , V , VII
  • 7.
  • 8.
    n-Butane CH3-CH2-CH3 C – C– C – C H H HH HH H H H H 1 432 Kekule structure Skeletal structure condensed structure
  • 9.
    Possible rotation forn-Butane C – C – CH2-CH3 H HH HH 1 2 H3C – C – C – CH3 HH H H 32 Rotation around C1 and C2 Rotation around C2 and C3 Structure I Structure II *
  • 10.
    Conformations of n-Butane •Butane has three carbon-carbon single bond and molecule can rotate about each of them . • If the rotation will be about C2 and C3 bond then confirmation will be symmetrical. • Different conformation of butane can be obtained by rotating about its middle carbon- carbon single bond.
  • 11.
    60° 120° 360° 300° 240° 180° H3C H3CH3C H3C CH3 CH3 CH3CH3 CH3 H3C CH3 CH3 H3C CH3 H HH H H HH H H H H H HH H H H H H H H H H H H H H H (I)-Fully Eclipsed Very high Repulsion Very high Energy Least stable (II) – Staggered(Gauche) Moderate Repulsion Moderate Energy Moderately stable (III)-Partly Eclipsed Repulsion high Energy high Less stable (IV)-Staggered (Anti) Repulsion less Energy less More stable (VII)-Fully Eclipsed Very high Repulsion Very high Energy Least stable (VI) – Staggered(Gauche) Moderate Repulsion Moderate Energy Moderately stable (V)-Partly Eclipsed Repulsion high Energy high Less stable
  • 12.
    Conformers of n-Butane •Butane has 3 staggered (II,IV,VI) conformer. • IV (Anti conformer), in which the two methyl group are as far apart as possible is more stable and require very less energy. • II , VI (Gauche conformer) • Butane has 3 eclipsed (I/VII,III,V) • I and VII are fully eclipsed • III and V are Partly eclipsed
  • 13.
    Energy level • Potentialenergy of I,VII is greater followed by III,V and II,VI. Conformer IV require very less energy because bulky group CH3 is far apart. • Stability of IV is greater than that of II,VI followed by III, V and I,VII. I ,VII > III, V > II, VI > IV IV > II, VI > III, V > I, VII
  • 14.
  • 15.
    Conformation for n-Butane C– C – CH2-CH3 H HH HH 1 2 Structure I
  • 16.
    60° 120° 360° 300° 240° 180° H3C H3C H3C CH2-CH3 CH3 CH3 CH3 H3C-H2C CH3 H HH H H H H H H H H H HH H H H H H HH H H H H H H H CH2-CH3CH2-CH3 CH2-CH3 H3C-H2C H3C-H2C (I)- Eclipsed Repulsion more Energy more Less stable (II) - Staggered Repulsion less Energy less More stable (III)-Eclipsed Repulsion more Energy more Less stable (IV)-Staggered Repulsion less Energy less More stable (VI)-Staggered Repulsion less Energy less More stable (V)-Eclipsed Repulsion more Energy more Less stable (VII)-Eclipsed Repulsion more Energy more Less stable
  • 17.
    Energy level • Bydoing so six possible confirmation can be obtained out of which 3 are staggered (II,IV,VI) and 3 are eclipsed form (I/VII,III,V). • Potential energy of I,III,V,VII is greater than that of II,IV,VI due to repulsive forces. • Stability of II,IV,VI is greater than that of I,III,V,VII. I , III, V, VII > II , IV , VI II, IV, VI > I , III , V , VII
  • 18.
    Thank you mydear students...!!!