Organic Chemistry"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 amine ammonia anhydride anion aryl base benzene benzylic carbon atom carbon-carbon carbonyl group carboxylic acids cation CH₁ CH₂ CH3 CH3 CH3 H chemical CO₂H compounds conformation conjugate delocalization derivatives diethyl ether double bond electrons electrophilic enantiomers energy enol epoxides ester ethanol ethylene Figure formation formed Grignard reagent H CH3 H H H H₂C H₂O halogen heat hydrogen bromide hydrogen halides hydrolysis hydroxide hydroxyl iodide isomers kcal/mol ketone kJ/mol leaving group Lithium mechanism methyl methyl group molecular formula molecular model molecule nitrogen nmr spectrum nucleophilic substitution orbital oxidation oxygen positive charge prepared primary PROBLEM propane proton react reaction reactive resonance ring SAMPLE SOLUTION secondary Section sodium sp˛ hybridized spł stable step stereogenic center stereoisomers structural formulas sulfuric synthesis synthetic tert-butyl tertiary tetrahedral intermediate tion yield