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3.6 - Organic Analysis

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Total cards: 9•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

How do you represent the time of flight ionisation equations?

Back (Answer)

M(g) + e- -> M+• + 2e- M+• = molecular ion or radical cation

#2
Front (Question)

Where does fragmentation occur to give a major peak?

Back (Answer)

At an acyl group RCO

#3
Front (Question)

How do you draw write a fragmentation equation using CH3COCH3?

Back (Answer)

[CH3COCH3]+• -> CH3CO (+ on the C) + CH3 (• on the C) The + and the • could also be on opposite molecules but the + on the acyl is more stable

#4
Front (Question)

What is the base peak?

Back (Answer)

RCO (+ on the C) The most common Most stable Easiest to form Always has 100% relative abundance

#5
Front (Question)

What should you watch out for with mass spectrometry graphs?

Back (Answer)

Chlorine and Bromine have 2 isotopes that appear Cl35 and Cl37 1:3 ratio Br79 and Br81 1:1 ratio So there will be more peaks two units apart (There are different combos of the isotopes)

#6
Front (Question)

What is the full scale in infrared spectroscopy?

Back (Answer)

4000 - 400

#7
Front (Question)

What is the difference in peaks of O-H alcohol and O-H acid?

Back (Answer)

O-H alcohol = perfect isolated curve O-H acid = merges in to the spikes of C-H bonds therefore very wide

#8
Front (Question)

What does the C≡N peak look like?

Back (Answer)

Tiny range so looks like a needle

#9
Front (Question)

How should you approach matching Infrared spectroscopy graphs to compounds?

Back (Answer)

Label the main identifying features of the graph, such as functional groups