First year mechanisms
  Second year mechanisms
  Third year mechanisms:
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      Free Radicals
      Option one
      Pericyclic Reactions
      Stereoselectivity
      Synthesis
      Transition metal chemistry
  All mechanisms
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Option one Mechanisms
Displaying 44 mechanisms:
Molecular materials and polymers- Dyes- Chemoluminescence
Molecular materials and polymers- Dyes- Phenolphthalien as a pH indicator
Molecular materials and polymers- Dyes- Photoinduced electron transfer
Molecular materials and polymers- Dyes- Photoinduced electron transfer- Ion detector (anthracene derivative)
Molecular materials and polymers- Dyes- Photoinduced electron transfer- pH indicator (anthracene derivative)
Molecular materials and polymers- Dyes- Reactive binding to fibre
Molecular materials and polymers- Dyes- Synthesis of Azo dyes
Molecular materials and polymers- Dyes- Synthesis of cyanines
Molecular materials and polymers- Organic conductors- Polyacetylene- Durham synthesis
Molecular materials and polymers- Organic conductors- Polyacetylene- Ziegler-Natta synthesis
Molecular materials and polymers- Organic conductors- Polyparaphenylene- preparation from Diels-Alder route
Molecular materials and polymers- Organic conductors- Polyparaphenylene- preparation from oxidation of benzene
Molecular materials and polymers- Organic conductors- Polyparaphenylene- preparation of PPP planar ladder
Molecular materials and polymers- Organic conductors- Polyparaphenylene- preparation via modified ICI route
Molecular materials and polymers- Polymers- Chain growth polymerisation- Anionic ring opening
Molecular materials and polymers- Polymers- Living polymerisation- Anionic
Molecular materials and polymers- Polymers- Living polymerisation- Atom transfer radical polymerisation (ATRP)
Molecular materials and polymers- Polymers- Living polymerisation- Radical
Molecular materials and polymers- Polymers- Living polymerisation- Ring opening metathesis (ROMP)
Molecular materials and polymers- Polymers- Step growth polymerisation- PET
Organometallics option- Arene chromium tricarbonyl complexes- Aryl anion as nucleophile
Organometallics option- Arene chromium tricarbonyl complexes- Aryl anion from removal of TMS group
Organometallics option- Arene chromium tricarbonyl complexes- Benzylic anion as nucleophile
Organometallics option- Arene chromium tricarbonyl complexes- Nucleophilic aromatic addition
Organometallics option- Arene chromium tricarbonyl complexes- Nucleophilic aromatic addition- formation of benzaldehyde
Organometallics option- Arene chromium tricarbonyl complexes- Nucleophilic aromatic addition- indol
Organometallics option- Arene chromium tricarbonyl complexes- Nucleophilic aromatic addition- with methoxy substituent
Organometallics option- Arene chromium tricarbonyl complexes- Nucleophilic aromatic addition- with methoxy substituent- intramolecular
Organometallics option- Arene chromium tricarbonyl complexes- Nucleophilic aromatic substitution
Organometallics option- Arene chromium tricarbonyl complexes- Preparation
Organometallics option- Arene chromium tricarbonyl complexes- Reduction of attached carbonyl- stereoselectivity
Organometallics option- Arene chromium tricarbonyl complexes- SN1 via carbonium ion
Organometallics option- Arene chromium tricarbonyl complexes- Stereochemistry of nucleophilic substitution of alpha leaving group
Organometallics option- Iron chemistry- η2 alkene complexes- Conversion of epoxides to alkenes
Organometallics option- Iron chemistry- η2 alkene complexes- Synthesis
Organometallics option- Iron chemistry- η2 alkene complexes- Synthesis of β-Lactams
Organometallics option- Iron chemistry- η2 alkene complexes- Synthesis of four membered amide rings
Organometallics option- Iron chemistry- η4 alkene complexes- Decomplexation
Organometallics option- Iron chemistry- η4 alkene complexes- Synthesis
Organometallics option- Iron chemistry- η5 alkene complexes- Nucleophilic attack
Organometallics option- Iron chemistry- η5 alkene complexes- Synthesis
Organometallics option- Iron chemistry- Fp- Reduction of Fp2 to Fp-
Organometallics option- Iron chemistry- Fp- Decomplexation to Fp alkyls to form carbonyl compounds
Organometallics option- Iron chemistry- Fp- Synthesis of Fp2