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Flashcards · 9701 · AS Topic 16
Hydroxy compounds (AS Level) flashcards
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16.1 Alcohols
- Oxidation products of primary, secondary and tertiary alcohols
- Primary: aldehyde, then carboxylic acid. Secondary: ketone (no further). Tertiary: not oxidised.
- Primary alcohol with acidified K₂Cr₂O₇: how do you get the aldehyde rather than the acid?
- Distil as it forms, so the aldehyde leaves before it is oxidised further. Heating under reflux with excess oxidant gives the carboxylic acid.
- Colour change when acidified dichromate(VI) oxidises an alcohol
- Orange → green (Cr₂O₇²⁻ → Cr³⁺). A tertiary alcohol leaves it orange.
- Dehydration of an alcohol
- Heat with concentrated H₂SO₄ or H₃PO₄ (about 170 °C): elimination of water gives an alkene.
- Alcohols with sodium, and with PCl₅
- Na: sodium alkoxide + hydrogen (effervescence). PCl₅: chloroalkane + HCl + POCl₃ (misty fumes of HCl).
- Why are alcohols weaker acids than water?
- The electron-donating alkyl group makes the O–H hydrogen less easily released and makes the alkoxide ion (RO⁻) less stable than OH⁻.
- Iodoform test: which alcohols give a positive result?
- Those containing CH₃CH(OH)–, e.g. ethanol and propan-2-ol. Warm with alkaline I₂(aq): yellow precipitate of CHI₃.