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Chapter 16 - Organic Analysis

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

how can you test for alkenes

Back (Answer)

add bromine water brown to colourless when alkene present

#2
Front (Question)

how can you test for tertiary alcohols

Back (Answer)

add acidified potassium dichromate if nothing happens (remains orange) then tertiary alcohol present

#3
Front (Question)

why does acidified potassium dichromate remain orange when a tertiary alcohol is added

Back (Answer)

because acidified potassium dichromate is an oxidizing agent, and tertiary alcohols cannot be oxidised.

#4
Front (Question)

how can you distinguish between aldehyde and ketones

Back (Answer)

add tollens reagent silver mirror forms for aldehydes or add Fehling’s solution brick red precipitate forms if aldehyde present

#5
Front (Question)

how can you test for a carboxylic acid

Back (Answer)

add sodium carbonate effervescence means acid is present

#6
Front (Question)

what is low resolution mass spectrometry useful for and why

Back (Answer)

for testing between samples of different substances because it isnt as expensive as high res spectrometry and still gives accurate results to 1dp

#7
Front (Question)

what is high resolution mass spectrometry useful for and why

Back (Answer)

for testing between samples of substances with different molecular formulae but same MR it gives the precise m/z ratio to 5dp

#8
Front (Question)

why are fragment peaks often bigger than the actual sample peaks

Back (Answer)

because fragmentation of molecules occurs very often leading to a greater ratio of fragments to whole molecules

#9
Front (Question)

what leads to fragmentation

Back (Answer)

when energetically unstable molecular ions dissociate

#10
Front (Question)

what is a molecular ion

Back (Answer)

a molecule with a single positive charge

#11
Front (Question)

how can mass spectra with fragmentation be useful

Back (Answer)

analysis can provide useful information about the structure of the molecule

#12
Front (Question)

how can you determine the m/z ratio of the whole molecule form a fragmentation spectrum

Back (Answer)

the highest m/z ratio is of the whole unfragmented molecule, not highest peak

#13
Front (Question)

whats the mr of a CH3+ fragment

Back (Answer)

15

#14
Front (Question)

whats the mr of a O+ fragment

Back (Answer)

16

#15
Front (Question)

whats the mr of a OH+ fragment

Back (Answer)

17

#16
Front (Question)

whats the mr of a CN+ fragment

Back (Answer)

26

#17
Front (Question)

whats the mr of a C2H3+ fragment

Back (Answer)

27

#18
Front (Question)

whats the mr of a C2H4+ or CO+ fragment

Back (Answer)

28

#19
Front (Question)

whats the mr of a C2H5+ or CHO+ fragment

Back (Answer)

29

#20
Front (Question)

whats the mr of a C3H7+ or C2H3O+ fragment

Back (Answer)

43

#21
Front (Question)

whats the mr of a C4H9+ or C3H5O+ fragment

Back (Answer)

57

#22
Front (Question)

whats the mr of a C5H11+ or C4H7O+ fragment

Back (Answer)

71

#23
Front (Question)

why do molecules absorb some IR light

Back (Answer)

because when their bonds vibrate at the same frequency as the wave, they absorb it this doesnt apply to molecules made of one element

#24
Front (Question)

how does IR spectroscopy work

Back (Answer)

a beam of IR is passed through a sample cell (with the sample in it) and a reference cell (with nothing in it). as the IR passes through the sample, some wavelengths of IR are absorbed by the bond’s vibrations so that the IR that comes out has lower transmittance for certain wavelengths the exiting waves are detected, and spectrums are produces which have peaks for the wavelengths have been absorbed