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Conformational
Analysis of
Cyclo butane:
Submitted to:
Prof. Abida Ashraf
Submitted by:
Sidra
MP-CHE-04
1st Semester
Stereochemistry CHE-533
M.Phil Organic Chemistry
Session: 2020-2022
The Women University Multan.
Content:
1. Cyclobutane
2. Conformations of cyclobutane
3. Inversion of Cyclobutane
4. Conformational analysis of cyclobutane
5. Representation by Ball and stick model
1.Cyclobutane:
• It is 4 membered ring in two dimensions with
angle 90 degree rather than 109.5 degree.
• There would be 8 pair of eclipsed hydrogen
atoms, which account for 26.3kcal/mol and
110kJ of total strain energy. angle strain is 109.5-
90= 19 degree.
2.Conformations of Cyclobutane:
Puckered Cyclobutane:
• Puckering which can
cause lowering the
torsional strain energy and
increase in the bond angle.
• Still there is lot of angle
strain but less than
cyclopropane.
Puckered to Butterfly form:
In 3D , the cyclobutane is flexible enough to buckle into butterfly
shape relieving torsional strain.
Puckered confirmation
3.Inversion Of Cyclobutane:
Cyclobutane undergoes ring inversion, its mean one puckered
form can easily change to other form by passing through a
transition state in which the ring is planner.
The barrier to inversion in cyclobutane is 1.45kcal/mol
(5.5kJ/mol)
Puckered structure( ring flip)
4.Conformational analysis of Cyclobutane:
Newman projection:
• Eclipsed Conformation:
• Staggered conformation
5.Ball and stick Model:
Linear cyclobutane: Puckered Cyclobutane:
Staggered Confirmation
Reference:
• Chapter # 4, Organic Chemistry by Dr. Wong yau
Hsiung
• Chem.libretexts.org
• Organic conformation analysis by David A. Lightner,
Jerome E. Gurst.
Conformational analysis

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Conformational analysis

  • 2. Submitted to: Prof. Abida Ashraf Submitted by: Sidra MP-CHE-04 1st Semester Stereochemistry CHE-533 M.Phil Organic Chemistry Session: 2020-2022 The Women University Multan.
  • 3. Content: 1. Cyclobutane 2. Conformations of cyclobutane 3. Inversion of Cyclobutane 4. Conformational analysis of cyclobutane 5. Representation by Ball and stick model
  • 4. 1.Cyclobutane: • It is 4 membered ring in two dimensions with angle 90 degree rather than 109.5 degree. • There would be 8 pair of eclipsed hydrogen atoms, which account for 26.3kcal/mol and 110kJ of total strain energy. angle strain is 109.5- 90= 19 degree.
  • 5. 2.Conformations of Cyclobutane: Puckered Cyclobutane: • Puckering which can cause lowering the torsional strain energy and increase in the bond angle. • Still there is lot of angle strain but less than cyclopropane.
  • 6. Puckered to Butterfly form: In 3D , the cyclobutane is flexible enough to buckle into butterfly shape relieving torsional strain. Puckered confirmation
  • 7. 3.Inversion Of Cyclobutane: Cyclobutane undergoes ring inversion, its mean one puckered form can easily change to other form by passing through a transition state in which the ring is planner. The barrier to inversion in cyclobutane is 1.45kcal/mol (5.5kJ/mol) Puckered structure( ring flip)
  • 8.
  • 9. 4.Conformational analysis of Cyclobutane: Newman projection: • Eclipsed Conformation: • Staggered conformation
  • 10. 5.Ball and stick Model: Linear cyclobutane: Puckered Cyclobutane: Staggered Confirmation
  • 11. Reference: • Chapter # 4, Organic Chemistry by Dr. Wong yau Hsiung • Chem.libretexts.org • Organic conformation analysis by David A. Lightner, Jerome E. Gurst.