|  |  |  |  | |||||||||||||
| Organic Acids and Bases | ||||||||||||||||
|  | ||||||||||||||||
| In this module we will begin to examine some of the properties of organic molecules that are important in determining their reactivity - particularly the acidity of H-atoms in those molecules. 'Nucleophiles' commonly have an electron lone pair produced by loss of a proton from a molecule and can act as reagents where the lone pair forms a bond to a suitable atom in another molecule. We will examine the characterisitcs of 'nucleophiles' and 'electrophiles' and ways of representing the process of reaction between them. | ||||||||||||||||
|  | ||||||||||||||||
|  Acidity and Basicity of Organic Molecules  Factors Affecting Acidity and Basicity  Factors Affecting Acidity 2  Electronegativity Effects  Effect of Carbon Hybridisation 1 | ||||||||||||||||
|  Effect 
      of Carbon Hybridisation 2  Charge 
      Delocalisation in Conjugate Bases  Charge 
      Delocalisation Effects on Acidity  Session 
      Summary  Contacting 
      ChemCAL Online | ||||||||||||||||
|  | ||||||||||||||||
|  | ||||||||||||||||