Does all alcohol undergo halogenation and controlled oxidation?

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    Alcohol Oxidation
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The discussion centers on the oxidation of t-butanol (tertiary butanol) and its structural integrity during the process. It highlights that t-butanol cannot be oxidized using potassium permanganate (KMnO4) without losing its t-butyl structure, as tertiary alcohols are resistant to oxidation under these conditions. The conversation also invites participants to share their knowledge of the three isomers of butanol, which include n-butanol, isobutanol, and t-butanol, each differing in structure and reactivity. The inability to oxidize t-butanol effectively underscores its unique chemical properties compared to its isomers.
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This is the question from the lab of "comparision of three isomers of butanol" GR 12 pg 84
 
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Could you oxidize t-butanol and still maintain the t-butyl structure? Tell us about the three isomers of butanol you are familiar with, please.
 
there is no reaction if you try to oxidise t-butanol (tertiary alcohol) with kmno4.
 

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