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A Level H2 Chemistry: Your 30‑Minute Organic Synthesis Roadmap

By Intuitional Team1 min read

A compact way to recall reagents, conditions and functional‑group interconversions under exam pressure.

A Level H2 Chemistry: Your 30‑Minute Organic Synthesis Roadmap

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