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3.3.6 Organic Analysis

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Total cards: 16•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

how could you test for alkenes? what is the result?

Back (Answer)

shake with bromine water, result is bromine water is decolourised (orange to colourless)

#2
Front (Question)

how do you test for haloalkanes? what is the result?

Back (Answer)

add NaOH (aq) and warm, acidify with HNO3, add AgNO3 (aq) result: precipitate of AgX (for Cl- = white, for Br = cream, for I = yellow.

#3
Front (Question)

how do you test for alcohols? what is the result?

Back (Answer)

acidified potassium dichromate and heat result: colour change from orange to green for primary and secondary alcohols no change for tertiary alcohols

#4
Front (Question)

how do you test for aldehydes? what is the result?

Back (Answer)

Fehling’s solution - brick red ppt. forms (from blue solution) Tollen’s reagent - silver mirror - Ag(s) ppt. forms

#5
Front (Question)

how do you test for carboxylic acids? what is the result?

Back (Answer)

sodium (hydrogen) carbonate (aq) result: CO2(g) given off, effervescence

#6
Front (Question)

What is mass spectrometry? how does it work?

Back (Answer)

used to find the relative molecular masses of organic compounds compound is dissolved in solution, ionised by high voltage supply (to 1+ ions), accelerated by a negatively charged plate, becomes a beam of ionised molecules, reach detector and cause a current to flow. Time of flight used to work out m/z value and plot graph.

#7
Front (Question)

what does the x axis show on a mass spectrum? What does this effectively show and why?

Back (Answer)

shows m/z value (mass divided by ionic charge) since most ions are 1+ , this effectively shows Mr

#8
Front (Question)

why are there multiple peaks when molecules are put into a mass spectrometer?

Back (Answer)

molecular ion is shown as a peak, but it will also fragment into smaller molecules, so these peaks are shown as well also, due to isotopes of atoms, different peaks may be seen

#9
Front (Question)

why do atoms and chemical bonds absorb infrared radiation?

Back (Answer)

they are constantly vibrating - they can absorb infrared radiation that is the same frequency as their frequency of vibration

#10
Front (Question)

what effect does a stronger bond have on the frequency of vibration?

Back (Answer)

vibrate faster (with higher frequency)

#11
Front (Question)

what effect do heavier atoms have on the frequency of vibration?

Back (Answer)

vibrate slower (with lower frequency)

#12
Front (Question)

how does infrared spectroscopy work?

Back (Answer)

• every bond has a unique vibration frequency in the infrared region of the EM spectrum • bonds absorb radiation that has the same frequency as their frequency of vibration • infrared radiation emerged from a sample is missing the frequencies that have been absorbed - can be used to identify a molecule’s functional group

#13
Front (Question)

what happens inside an infrared spectrometer?

Back (Answer)

beams of infrared radiation with a range of frequencies is passed through the sample radiation that emerges is missing frequencies that have been absorbed by the bonds in the sample. graph is plotted of intensity against frequency of radiation

#14
Front (Question)

what do troughs on an infrared spectrum show?

Back (Answer)

the frequencies where radiation has been absorbed - match to table to find out which bonds they represent

#15
Front (Question)

what is the fingerprint region?

Back (Answer)

area of IR spectrum below wave number 1500 many peaks caused by complex vibrations of the whole molecule, unique to every compound, so can be used to identify compounds.

#16
Front (Question)

how is the fingerprint region used to identify compounds?

Back (Answer)

fingerprint region’s pattern is matched to a database on a computer to identify the compound accurately