Oxidation-Primary Alcohol Simplified Revision Notes for Scottish Highers Chemistry
Revision notes with simplified explanations to understand Oxidation-Primary Alcohol quickly and effectively.
Learn about Oxidation of Alcohols for your Scottish Highers Chemistry Exam. This Revision Note includes a summary of Oxidation of Alcohols for easy recall in your Chemistry exam
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Oxidation of Primary Alcohol
Understanding Oxidation:
In chemistry, we use oxidation as a term to describe a specific type of chemical reaction. Oxidation involves changes in the O (oxygen to hydrogen) ratio within a molecule.
To better understand this concept, let's explore the oxidation of ethanol, a primary alcohol.
Ethanol Oxidation:
Ethanol (C2​H5​OH) is a primary alcohol. When it undergoes oxidation, it experiences a change in its O ratio.
In the first step of oxidation, ethanol is oxidised to produce ethanal (also known as acetaldehyde) by removing two hydrogen atoms. This process involves breaking carbon-hydrogen (C-H) bonds and forming a carbon-oxygen (C=O) double bond:
The O ratio changes from 1:6 in ethanol to 1:4 in ethanal. This change signifies the oxidation process.
In the second step, ethanal is further oxidised to produce ethanoic acid (also known as acetic acid) by adding an oxygen atom. This involves breaking the carbon-oxygen (C=O) double bond in ethanal and forming two carbon-oxygen (C-O) single bonds:
As a result, the O ratio changes from 1:4 in ethanal to 1:2 in ethanoic acid.
Conclusion:
The oxidation of a primary alcohol, such as ethanol, involves a sequence of chemical reactions.
It begins with the conversion of the alcohol into an aldehyde (ethanol to ethanal) by removing hydrogen atoms, followed by further oxidation to produce a carboxylic acid (ethanal to ethanoic acid) by adding oxygen atoms.
The change in the O ratio from 1:6 (ethanol) to 1:4 (ethanal) to 1:2 (ethanoic acid) serves as a clear indicator of the oxidation process.
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