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Module 4: Analysis

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

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#1
Front (Question)

Mass spectrometry What happens in the mass spectrometry

Back (Answer)

High energy electron bombards a molecules in a mass spectrometer which results in the molecule losing an electron

#2
Front (Question)

Mass spectrometry What is the resulting species when a molecule is bombarded by the higher energy electron

Back (Answer)

Molecular ion

#3
Front (Question)

Mass spectrometry Equation for formation of molecular ion

Back (Answer)

Molecule —-> Molecule+. + e-

#4
Front (Question)

Mass spectrometry Notation for molecular ion

Back (Answer)

M+

#5
Front (Question)

Mass spectrometry What is the definition of a molecular ion

Back (Answer)

Positive ion formed when molecule loses an electron

#6
Front (Question)

Mass spectrometry What is on the axis of a spectra

Back (Answer)

X- m/z -mass to charge ratio Y- %abundance

#7
Front (Question)

Mass spectrometry Where is the M+ ion on a spectra

Back (Answer)

Last peak on the right

#8
Front (Question)

Mass spectrometry What is fragmentation

Back (Answer)

Process in mass spec that causes positive ion (M+) to split into pieces of a positive ion (which produces a peak) and a radical

#9
Front (Question)

Mass spectrometry What is the M+1 peak

Back (Answer)

Smallll peak just after M+

#10
Front (Question)

Mass spectrometry Why is the M+1 peak there

Back (Answer)

Due to C-13 present

#11
Front (Question)

Mass spectrometry How is it used for isotopes

Back (Answer)

Positions of peaks show different isotopes prescence and is used to find relative atomic mass with abundance

#12
Front (Question)

Mass spectrometry How can organic molecules be identified from eac other

Back (Answer)

Each have different peaks from fragments

#13
Front (Question)

Mass spectrometry How does fragmentation occur and how does it show on spectra

Back (Answer)

One bond broken in the M+ to form a positive ion and radical Peak at the positive ion formed with its m/z value (mr)

#14
Front (Question)

Mass spectrometry Where is the Mr of the whole product found

Back (Answer)

At the M+ ion

#15
Front (Question)

Mass spectrometry For analysis questions what is the typical way to find the molecular formula

Back (Answer)

Find the empirical formula and find mr Find mr of whole product at the M+ peak mr of whole product / Mr of empirical Scale up the ration of the empirical formula

#16
Front (Question)

Mass spectrometry What are fragmentation patterns of functional groups

Back (Answer)

Specific positions of peaks and differences between major peaks which makes it possible to identify the type of compound

#17
Front (Question)

Mass spectrometry What is the peak due to at m/z 15

Back (Answer)

CH3+

#18
Front (Question)

Mass spectrometry What is the peak due to at m/z 29

Back (Answer)

C2H5+

#19
Front (Question)

Mass spectrometry What os the peak due to at m/z 43

Back (Answer)

C3H7+

#20
Front (Question)

Mass spectrometry For alkanes what affects the abundance of a peak

Back (Answer)

The stability of the carbo cation

#21
Front (Question)

Mass spectrometry For alkanes as the stability of the carbocation increases what happens to the peak

Back (Answer)

Larger abundance

#22
Front (Question)

Mass spectrometry For haloalkanes why is there often multiple peaks in the molecular ion region

Back (Answer)

Due to the different isotopes of the halogen

#23
Front (Question)

Mass spectrometry For ketones and aldehydes what is the characteristic fragmentation

Back (Answer)

Cleavage of bonds next to carbonyl (C=O)

#24
Front (Question)

Mass spectrometry Where do carbonyl compound fragments

Back (Answer)

Ether side of the carbonyl group