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Heterocyclic Aromatic Compounds
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2-position addition alcohol alkyl halides amines analogous angle strain anion antiperiplanar aromatic compounds atomic orbitals attack axial base benzene bonding orbital bromine carbanion carbon atoms carbonium ion carbonyl group catalysis cation CH3 CH3 Chapter chemical chloride concentration conformation conjugated Cotton effect cyclic cycloaddition cyclobutadiene cyclohexane cyclooctatetraene cyclopentadienyl delocalization derivatives discussed double bond electrophilic electrophilic addition-with-elimination reactions elimination reactions enolate equation equatorial equilibrium ester ethylene example formation free energy furan Hammett heterocyclic Hiickel hydrogen atom hydrolysis hydroxide interaction intermediate involving iodide ionization kcal mole-1 ketones kinetic kJ mole-1 leaving group molecular orbital molecule nitration nitrogen atom non-bonding nucleophilic occur olefin organic chemistry oxidation oxygen atom pair phosphine phosphorus proton pyridine pyrrole rate constant react reactants reactive readily reagents rearrangement resonance salt solution solvent solvolysis sp2 hybrid stable steric steric strain structures substitution sulphonation synthesis t-butyl temperature theory thiophen tt electrons undergo unimolecular yield ylids