OCR A-Level Chemistry H432
Foundations in Chemistry
Bonding and Structure
Periodic Table and Energy
Enthalpy Changes
Chemical Equilibrium
Basic Concepts of Organic Chemistry
Core Organic Chemistry
Alkenes
Organic Synthesis
How Fast?
Physical Chemistry and Transition Elements
Acids, Bases and Buffers
Redox and Electrode Potentials
Transition Elements
Aromatic Compounds
Organic Chemistry and Analysis
Spectroscopy
Spectroscopy
- 8 subtopics
- 19 things to know
- Components 02 and 03
What Spectroscopy covers
Carbon-13 and proton NMR and what each feature of a spectrum tells you, and then the combination of elemental analysis, mass spectrometry, infrared and NMR that settles a structure.
Where it is assessed
Components 02 and 03
Synthesis and Analytical Techniques, then the unified paper.
Check the OCR specification ↗The 8 subtopics
Each one has its own page.
- Carbon-13 and proton NMR: peaks, chemical shift and integrationRecall questions on what the number of peaks and the chemical shift indicate in each kind of NMR, what proton decoupling means, and what integration gives.Open →
- Spin-spin splitting and predicting a spectrumRecall questions on the n + 1 rule, what a singlet, doublet, triplet and quartet each indicate, and predicting a spectrum from a structure.Open →
- TMS, deuterated solvents and the D₂O shakeRecall questions on tetramethylsilane as the NMR reference standard, deuterated solvents such as CDCl₃, and using a D₂O shake to identify O–H and N–H protons.Open →
- Combining elemental analysis, mass spectrometry, IR and NMRRecall questions on what each technique contributes, why one alone is not enough, and how they are used together to separate possible isomers.Open →
- Molecular formula from the molecular ion, and fragmentation lossesRecall questions on scaling an empirical formula with the molecular ion peak, and on what losses of 15, 17, 29 and 45 mass units suggest.Open →
- What IR and NMR each contribute to a structureRecall questions on identifying functional groups from infrared absorptions and the fingerprint region, and on what chemical shift, integration and splitting each add.Open →
- Infrared absorption, global warming and breathalysersRecall questions on how covalent bonds absorb infrared radiation, greenhouse gases and the evidence linking carbon dioxide to global warming, and infrared monitoring of exhaust gases and breathalysers.Open →
- A systematic approach and the degree of unsaturationRecall questions on the order in which the techniques are applied, calculating the degree of unsaturation, and why a carbon-13 spectrum may show fewer peaks than carbons.Open →
What you need to know
Answer each one before you reveal it.
What does a singlet in proton NMR indicate about adjacent protons?
What compound is used as the reference standard for chemical shift measurements in NMR spectroscopy?
Why are deuterated solvents such as CDCl₃ used when running NMR spectra?
How can O–H and N–H protons be identified using D₂O in proton NMR?
What two pieces of information does mass spectrometry give, which technique turns an empirical formula into a molecular formula, and how are isomers with the same molecular formula told apart?
After dividing percentage compositions by relative atomic masses, what comes next, what does mass spectrometry provide, and how is the molecular ion mass then used?
How does infrared spectroscopy distinguish carboxylic acids and alcohols from aldehydes, ketones and esters, what does the number of ¹H NMR peaks show, and what do proton chemical shifts indicate?
What do carbon-13 chemical shifts indicate, which technique identifies functional groups in a systematic structure elucidation, and what is the final step?
What is the n+1 rule, and what do a singlet and a doublet say about neighbouring hydrogens?
What does a quartet in a ¹H NMR spectrum tell you about neighbouring hydrogens?
How does an infrared breathalyser measure the ethanol in a driver's breath?
Which two gases from car exhausts can be monitored using infrared spectroscopy?
Which bonds in carbon dioxide, water vapour and methane absorb infrared radiation in the atmosphere?
What does observing fewer ¹³C NMR peaks than carbon atoms indicate about the molecule?
Define degree of unsaturation (index of hydrogen deficiency).
What does 'proton decoupled' mean in the context of carbon-13 NMR spectra?
How do propan-1-ol and propan-2-ol differ in ¹³C NMR?
When determining molecular formula from empirical formula, what must first be calculated?
Take Spectroscopy further
The same content, four other ways.
Commonly confused
Pairs that lose marks when they are blurred together.
Chemical shift vs Integration trace
Chemical shift: resonance position measured relative to a reference signal. Integration trace: relative area showing the proton ratio in different environments.
Carbon-13 NMR vs Proton NMR
Carbon-13 NMR: spectroscopy showing distinct carbon environments. Proton NMR: spectroscopy showing hydrogen environments, ratios and splitting.
Molecular ion peak vs Fragment ion peak
Molecular ion peak: signal corresponding to the intact ionised molecule. Fragment ion peak: signal corresponding to a charged piece formed after bond breaking.
Questions from this topic
Each one with the model answer underneath.
- 1
In carbon-13 NMR spectroscopy, what does the number of peaks in a spectrum indicate?
Model answer
The number of different carbon environments in the molecule.
- 2
Why do equivalent carbon atoms produce only a single peak in carbon-13 NMR?
Model answer
Because they are in identical chemical environments and therefore resonate at the same frequency.
- 3
What information do chemical shift values provide in carbon-13 NMR?
Model answer
They indicate the type of carbon environment present in the molecule.
- 4
What does 'proton decoupled' mean in the context of carbon-13 NMR spectra?
Model answer
Each carbon environment appears as a single peak rather than being split by coupling to attached protons.
- 5
How can carbon-13 NMR data be used to deduce molecular structures?
Model answer
By combining the number of carbon environments with their chemical shift values to identify the types and arrangements of carbon atoms present.
- 6
In proton NMR spectroscopy, what does the number of peaks indicate?
Model answer
The number of different proton environments in the molecule.
What is inside Levo
Six ways to work the same material.
Spectroscopy revision questions
- What does Spectroscopy cover in OCR A-Level Chemistry?
- 8 subtopics: carbon-13 and proton nmr: peaks, chemical shift and integration, spin-spin splitting and predicting a spectrum, tms, deuterated solvents and the d₂o shake, combining elemental analysis, mass spectrometry, ir and nmr, molecular formula from the molecular ion, and fragmentation losses, what ir and nmr each contribute to a structure, infrared absorption, global warming and breathalysers and a systematic approach and the degree of unsaturation. Each one has its own page with questions and model answers.
- How is Spectroscopy organised?
- By the OCR H432 specification, subtopic by subtopic, so it matches the order you are taught it in.
Every question in Spectroscopy, on a schedule.
Attempt a question from memory, write the correct version, then attempt it again. Levo records the jump between your first attempt and your last, and brings each question back on the day you are due to forget it.
Or £46 a year, about £3.83 a month. Cancel anytime.