Created by jasmin.sahota
over 10 years ago
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Question | Answer |
oxidation of primary alcohols gives | Aldehydes |
If product | Distilled off as it forms |
The oxidising agent is | Acidified K2CrO7 |
Colour change | Orange to green |
But if refluxed with | excess K2CrO7 |
Then a | Carboxylic acid will form |
Give equation for partial oxidation of butan-1-ol | C4H9OH + [O] --> C3H7CHO + H2O |
And an equation to show full oxidation | C4H9OH + 2[O] --> C3H7COOH + H2O |
During the full oxidation what are the “conditions” | Reflux with an excess of acidified Cr2O72- |
What forms on oxidation of propan-2-ol | propanone |
Can you oxidiose this further? | No, Ketones cannot be oxidised |
Equation for oxidation of ethanal | CH3CHO + [O] --> CH3COOH |
Reagent for reduction of carbonyls | NaBH4 |
Conditions for this reaction | In aqueous or ethanolic soln and refluxed |
What forms when carbonyls are reduced | Alcohols |
Equation for reduction of propanone | CH3COCH3 + 2[H] --> CH3CH2OHCH3 |
Name of Mechanism for reaction | Nucleophilic addition |
What is the nucleophile | H- |
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