"A Market Leading, Traditional Approach to Organic Chemistry" Throughout all seven editions, Organic Chemistry has been designed to meet the needs of the "mainstream," two-semester, undergraduate organic chemistry course. This best-selling text gives students a solid understanding of organic chemistry by stressing how fundamental reaction mechanisms function and reactions occur. With the addition of handwritten solutions, new cutting-edge molecular illustrations, updated spectroscopy coverage, seamless integration of molecular modeling exercises, and state-of-the-art multimedia tools, the 7th edition of Organic Chemistry clearly offers the most up-to-date approach to the study of organic chemistry.
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acetic acid acyl chlorides alcohol aldehydes aldehydes and ketones alkanes alkenes alkyl group alkyl halides alkynes allylic amide amines ammonia anion aromatic substitution aryl attack base benzene benzylic carbon carbon atoms carbon-carbon carbonyl group carboxylic acids cation chapter Chemical shift chiral compounds conformation conjugate converted derivatives diethyl double bond electrons enantiomers energy enol epoxides equation ester ethanol ether ethylene example Figure formation formed give Grignard reagent H NMR halogen heat hybridization hydrocarbons hydrogen halides hydrolysis hydroxide hydroxyl iodide isomers IUPAC name kcal/mol ketone kJ/mol leaving group lithium mechanism methyl methyl group molecular formula molecular models molecule nitrogen NMR spectrum nucleophilic substitution orbital organic chemistry oxidation oxygen phenol polar prepared primary PROBLEM propane proton react reaction reactive resonance ring SAMPLE SOLUTION secondary Section shown sodium stable step stereogenic center stereoisomers structural formulas synthesis synthetic Table tertiary tetrahedral intermediate tion yield