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Biological Chemistry FIRST YEAR ORGANIC CHEMISTRY Lecture Eight Carboxylic acids + Esters Convenor : Dr. Fawaz Aldabbagh.

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Presentation on theme: "Biological Chemistry FIRST YEAR ORGANIC CHEMISTRY Lecture Eight Carboxylic acids + Esters Convenor : Dr. Fawaz Aldabbagh."— Presentation transcript:

1 Biological Chemistry FIRST YEAR ORGANIC CHEMISTRY Lecture Eight Carboxylic acids + Esters Convenor : Dr. Fawaz Aldabbagh

2 Carboxylic Acids We can distinguish a water-insoluble carboxylic acid and phenol from an alcohol

3 Highly Polar Low molecular weight acids show Appreciable Solubility in Water High Bpt – Extensive H-bonds to themselves and water Carboxylic Acids NAMES Methanoic acid Ethanoic acid Propanoic acid 4-Bromo-2-ethylpentanoic acid Ethanedioic acid (oxalic acid) rhubarb Red ants Terephthalic acid Phthalic acid

4 Esterification Alcohol part appears first in the name

5 Ester molecules cannot H-bond to each other, because they do not have an –OH Consequently, B.pt is much lower than that of alcohols and acids of comparable mass H-bonding to water is possible -low mw esters are soluble in water Solubility rapidly decreases with carbon chain length. Equilibrium reaction -Reversible with acid And water

6 Salicyclic acid is the active ingredient of aspirin. - It has analgesic, antipyretic and anti-inflammatory properties Buffered aspirin contains bases. Esters are also largely responsible for the flavour and smell of fruits and flowers Esters are hydrolysed in acid and base catalysed reactions

7 Ester Saponification - is the base-catalysed hydrolysis of an ester

8 Write a mechanism for the acid and base hydrolysis of a lactone

9 Redox Reactions Addition of Oxygen or Removal of Hydrogen is OXIDATION Removal of Oxygen or Addition of Hydrogen is REDUCTION

10 Examples of Reduction Reactions Examples of Oxidation Reactions


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