3.3.6 organic analysis Flashcards
how do you test for primary and secondary alcohols?
reagent: sample solution + potassium dichromate solution acidified with dilute sulphuric acid
positive: orange to green colour change
explanation : alcohol is oxidised so potassium dichromate is reduced to chromium ions
how do you test for alkenes?
reagent : shake sample solution with a few drops of bromine water
positive : orange to colourless
explanation : double bond breaks and a dibromoalkane is formed
how do you test for carboxylic acids?
reagent : add sodium carbonate
positive: fizzing bubbling or effervescence
explanation: acid base reaction occurs producing co2
how do you test for aldehydes using Tollens?
reagent : add tollens and warm
positive : silver mirror if aldehyde is present
explanation: tollens acts as an oxidising agent, oxidation of aldehyde
into a carboxylic acid, tollens reduced to solid silver
how do you test for aldehydes using fehlings?
reagent : add fehlings
positive: brick red precipitate
explanation: fehlings reagent is oxidising agent, oxidation of aldehyde into carboxylic acid
how do you test for halogenoalkanes ?
reagent: add NaOH then warm then add silver nitrate
positive: precipitate formed
explanation: nucleophilic substitution of halogenoalkane to form an alcohol
what colour precipitates do chloride, bromide and iodide form?
chloride : white
bromide : cream
iodide : yellow
what does mass spectroscopy do?
determine the m/z of a peak to several decimal places
can help distinguish between compounds that have very similar relative mrs
in infrared spectroscopy what is the fingerprint region?
part of infrared spectra that can be compared to a database to identify the molecule