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INTRODUCTION AND NOMENCLATURE
Oxirane or Ethylene Oxide
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1-oxide 7r-electron acetic anhydride alcohol aldehyde aliphatic alkali alkyl Amer amine amino ammonia anion aqueous aromatic attack azetidine aziridine benzene bromine carbon atoms carboxyl cation Chem Chemistry chloride colourless liquid Comm corresponding cyclization decarboxylation derivatives Diels—Alder reaction dimethyl dipole easily electrons electrophilic ester ether ethylene formation formed furan furfural gives Grignard reagents halides halogen heating heteroatom Heterocyclic Compounds hydrochloric acid hydrolysis hydroxide imidazole indole intermediate isolated isoquinoline J.C.S. Perkin kcal)/mole ketones lithium aluminium hydride methods methyl group methyl iodide mixture molecule nitration nitrogen atom nucleophilic obtained occurs oxepine oxidation oxirane oxygen penicillin peroxide phenyl phosphorus photolysis polymerization position potassium prepared presence proton purine pyrazole pyridine pyrimidine pyrrole quinoline reactive reacts readily reduction resonance energy resonance hybrid ring opening ring system salts shown similar sodium solvents spectrum stable structure substitution sulphuric acid synthesis tautomer tautomeric Tetrahedron Lett thiirane thiophene undergoes yields