A Level
A Level H2 Chemistry: Your 30‑Minute Organic Synthesis Roadmap
•By Intuitional Team•1 min read
A compact way to recall reagents, conditions and functional‑group interconversions under exam pressure.

Big picture
Think in functional groups and the arrows that convert them. Anchor reactions: oxidation–reduction, nucleophilic substitution, electrophilic addition, elimination, hydrolysis.
Core conversions
- Alkene → Alcohol: Acidic KMnO4 (diol) or H2SO4/H2O (Markovnikov).
- Alcohol → Halogenoalkane: PCl5, SOCl2, HX.
- Primary alcohol → Aldehyde → Carboxylic acid: PCC (partial) vs acidic dichromate (full).
- Carboxylic acid ↔ Ester: Fischer esterification / base hydrolysis.
- Nitrobenzene → Aniline: Sn/HCl followed by NaOH.
Exam habits
- Write reagents + conditions exactly (temp/pressure/catalyst).
- Check stereochemistry and regiochemistry.
- Account for by‑products and overall yield.
Build a one‑page map linking groups with arrows and annotate your favourite routes.
Tags
A LevelH2 ChemistryOrganic SynthesisReagentsMechanisms