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11. Measurement

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Total cards: 14•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (14)

#1
Front (Question)

Random Error

Back (Answer)

Above or below true value, usually due to equipment (repetition of at least 3, range of 5)

#2
Front (Question)

Systematic Error

Back (Answer)

In one direction, usually due to instrument / method error eg physical errors in the measuring device, improper or sloppy use of measuring device, ambient conditions

#3
Front (Question)

Precision

Back (Answer)

A measure of the certainty

#4
Front (Question)

Accuracy

Back (Answer)

How close the value is to the accepted value

#5
Front (Question)

Mass Spectroscopy Process

Back (Answer)

Ionization –> Acceleration –> Deflection –> Detection

#6
Front (Question)

Mass Spectroscopy requirements and info

Back (Answer)

• vacuum • callibrated with 12C • all living things composed w/ 12C • solid in room tempt –> easy to store and transport • abundant • Lighter ions/ positive charges deflect more • Mass/Charge ratio m/z

#7
Front (Question)

Infrared Spectroscopy

Back (Answer)

• Molecules that absorb infrared radiation have fluctuating dipole moments • When molecules absorb infrared radiation they can bend, stretch and/ or vibrate (symmetrically / asymmetrically) • I.R. Active mode of vibration

#8
Front (Question)

H1NMR (Nuclear Magnetic Resonance)

Back (Answer)

• Looks at protons in hydrogen atoms • proton spins act as magnets –> uses energy to line up with or against magnetic field –> energy measured in the radiowave region • chemical environments

#9
Front (Question)

Index of Hydrogen Deficiency (IHD)

Back (Answer)

• Degree of unsaturation in organic compounds • double bond/ ring = 1 degree • triple bond = 2 degree • aromatic ring = 4 degree • IHD = 0.5(2C + 2 - h - x - n)

#10
Front (Question)

High Resolution H1NMR

Back (Answer)

• Spin-spin coupling creates slightly different energy levels creating split in peaks • n + 1 rule • CH2 next to CH3 splits the CH3 peak into 3 • CH3 next to CH2 splits the CH2 peak into 4 peaks • CH next to CH3 splits the CH3 into 2 peaks • The proton on a hydroxyl group generally does not split • shields adjacent H protons as well

#11
Front (Question)

Tetramethylsilane (TMS) Standard

Back (Answer)

• Hydrogens are all in the same environment so only one reference line is produced given a value of σ=0ppm • Si has a lower electronegativity than C so Si-H lines do not overlap with C-H ones • Chemically intert, soluble organic solvents, can be easily removed by boiling

#12
Front (Question)

Xray Crystallography

Back (Answer)

• constructive interferance - when waves are in phase, they can be added together • used to determine bond length, bond angles and crystalline structure

#13
Front (Question)

Applications of IR Radiation

Back (Answer)

• TV remote • Heat sensor • Global warming • H2O and CO2 bonds that absorb IR radiation because of tehir fluctuating dipoles • UV high energy, shorter wavelength ; IR lower energy, longer wavelength

#14
Front (Question)

Applications of 1HNMR Spectroscopy

Back (Answer)

• Breathalyser • MRI scans • Magnetic resonance imaging –> non invasive • detects protons in 1H atoms of water molecules