Organic ChemistryThe sixth edition of this text is revised and now incorporates new information. Some chapters have been rewritten, making topics such as conjugation and nucleophilic substitution more accessible. Problems are provided which challenge the readers' understanding. read. |
Contents
Structure and Properties | 1 |
Methane Energy of Activation Transition State | 39 |
Alkanes FreeRadical Substitution | 77 |
Copyright | |
38 other sections not shown
Common terms and phrases
2-butene acetate addition alcohol aldehydes aliphatic alkanes alkenes alkyl group alkyl halides alkynes allyl amine anion aqueous aromatic ring aromatic substitution aryl attack base benzene benzyl bromide carbanion carbon carbon atoms carbon-carbon double bond carboxylic acids cation CH₁ CH₂ CH3 CH3 chemical chemistry chiral center chloride compounds configuration COOH diazonium Discussed in Sec double bond Eact electrons electrophilic electrophilic aromatic substitution enantiomers energy ester ether ethylene example formation formed formula free radicals Grignard reagent H H H H₂C H₂O halogen heat hydrocarbons hydroxide isomeric isomers isopropyl kcal ketones leaving group mechanism methyl molecular molecule n-propyl NH₂ nitrogen NMR spectrum nucleophilic substitution optically active orbitals organic oxidation oxygen pair phenol polar positive charge Problem proton racemic react reactants reaction reactivity rearrangement resonance salts sec-butyl SN2 reaction sodium soluble solvent spectra stability step stereochemistry stereoisomers structure substrate synthesis tert-butyl toluene transition undergo vinyl yield