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Secondary alcohols are oxidised to

ketones. There is no further reaction


which might complicate things. For
example, if you heat the secondary
alcohol propan-2-ol with sodium or
potassium dichromate(VI) solution
acidified with dilute sulphuric acid, you
get propanone formed.
Playing around with the reaction
conditions makes no difference
whatsoever to the product.
Using the simple version of the
equation:

Questions to test your understanding

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questions on making aldehydes and ketones

answers

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