Structure & bonding
Hybridisation, resonance, acidity and stereochemistry.
Clear notes on every reaction, practice that makes you predict products and push arrows, and synthesis problems worked backwards step by step.
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Hybridisation, resonance, acidity and stereochemistry.
SN1, SN2, E1, E2, additions and carbonyl chemistry.
Retrosynthesis and multi-step routes.
IR, NMR and mass spectrometry interpretation.
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Curved-arrow mechanisms and predicting products.
Multi-step routes from given starting materials.
Nomenclature, stereochemistry and spectroscopy.
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The mistakes that are specific to this exam, not generic study advice.
Memorising reactions without understanding mechanisms.
Not practising enough problems.
Ignoring stereochemistry in products.
Starting synthesis practice too late.
A sequence that suits this exam specifically.
Mechanism, then predict products.
Link functional groups by the reactions between them.
Work backwards from targets.
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