Topic 6 Tests Flashcards
How can a tertiary alcohol be distinguished from a primary (or secondary) alcohol?
Heat both with acidified potassium dichromate. The tertiary alcohol will remain in a yellow solution but primary and secondary alcohols will turn the solution green.
Explain why, during the oxidation of primary and secondary alcohols, the solution changes from yellow to green.
The yellow chromium (VI) ions are reduced to green chromium (III) ions.
The oxidation of alcohols using potassium dichromate does not distinguish between primary and secondary alcohols. Suggest how they could be distinguished between.
Oxidise the alcohols under distillation using acidified potassium dichromate and then add Fehling’s reagent. If the solutions turns red it is primary, if it remains blue it is a secondary alcohol.
Explain why the Fehling’s reagent turns red for primary alcohols and remains blue for secondary alcohols.
Fehling’s is a mild oxidising agent so in the presence of an aldehyde the blue copper(II) ions are reduced to red copper (I) ions. Ketones cannot be oxidised so remain blue.
Describe the process of testing which halogen is present in a halogenoalkane.
- Add drop of the halogenoalkane to aqueous sodium hydroxide and heat in a water bath. [Hydrolysis of the halogenoalkane]
- Acidify with dilute nitric acid.
- Add a few drops of silver nitrate solution.
Describe the colours of the following solid precipitates:
- AgCl(s)
- AgBr(s)
- AgI(s)
- White
- Cream
- Yellow
What is the general test for an alkene?
Add an excess of alkene to bromine water then it will go from brown to colourless.