tertiary
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Primary alcohols are more resistant to oxidation compared to secondary and tertiary alcohols. This is because primary alcohols have a hydrogen atom attached to the carbon with the hydroxyl group, which can be oxidized to form an aldehyde or carboxylic acid.
A secondary alcohol undergoes oxidation to yield a ketone; a primary alcohol forms an aldehyde instead, and a tertiary alcohol usually does not form either a ketone or an alcohol, because the carbon having the OH group in a tertiary alcohol already has three bonds to other carbon atoms and therefore cannot form a double bond to oxygen without more extensive breaking of other bonds in the tertiary alcohol.
OIL RIG. Oxidation is Loss, Reduction is Gain (of electrons, or of Hydrogen) Oxidation is gain of oxygen, reduction is loss of oxygen. In answer to your question, oxidation of a primary alkanol (alcohol) gives you an alkanal or aldehyde, and what is removed is an atom of H.
The product of the oxidation of a primary alcohol is a carboxylic acid.
After the oxidation of a hydroxyl group, you can obtain a carbonyl group.
This is an alcohol, and there are 2 stages of oxidation. First, it will be oxidized to the aldehyde, and then further oxidation will produce the acid.(1) CH3CH2CH2CH=O (2) CH3CH2CH3COOH