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Pharmaceutical organic chemistry II

Other Subjects of B Pharmacy 3rd Semester

Topic wise notes of:

Physical Pharmaceutics I

  • Solubility of Drugs
  • States & Properties of Matter
  • Surface, Interfacial Phenomenon
  • Complexation & Protein Binding
  • pH, Buffers & Isotonic Solutions

Topic wise notes of:

Pharmaceutical Microbiology

Unit V Summary: Cycloalkanes and Their Stability

Unit V explores the structure, stability, and reactivity of cycloalkanes, with a specific focus on smaller ring compounds such as cyclopropane and cyclobutane. Cycloalkanes are saturated hydrocarbons containing carbon atoms arranged in a ring, and their unique ring structures influence their chemical behavior and stability.

The unit begins with a discussion on the stability of cycloalkanes and introduces Baeyer’s strain theory, which suggests that ring strain arises from deviations in bond angles from the ideal tetrahedral angle (109.5°). According to Baeyer, smaller rings such as cyclopropane and cyclobutane are less stable due to significant angle strain.

However, Baeyer’s theory has limitations, which are addressed by Coulson and Moffitt’s modification, incorporating orbital interactions and modern bonding concepts to explain the actual geometry and strain in ring systems. The unit further explains the Sachse-Mohr theory, also known as the theory of strainless rings, which provides a more accurate depiction of stability in medium and large ring compounds by considering puckered conformations that relieve strain.

Finally, the unit details the chemical reactions of cyclopropane and cyclobutane, two highly strained and reactive cycloalkanes. These reactions highlight the impact of ring strain on chemical reactivity and provide insight into the unique behavior of small-ring systems in organic chemistry.

This unit lays the foundation for understanding ring strain, molecular geometry, and the reactivity of cyclic compounds, which is essential in both synthetic and medicinal chemistry.

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