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. |
Other editions - View all
Common terms and phrases
acetic acid acyl chlorides alcohol aldehydes aldehydes and ketones alkanes alkenes alkyl group alkyl halides alkynes allylic amide amines ammonia anhydride anion aromatic substitution aryl base benzene benzylic carbon atoms carbon-carbon carbonyl group carboxylic acids cation CH₁ CH₂ CH3 CH3 Chemical shift chiral CO₂H compounds conformation conjugate delocalization derivatives diethyl ether double bond electrons electrophilic enantiomers energy enol epoxides equation ester ethanol ethylene example Figure formed give Grignard reagent H CH3 H H H H NMR H₂O halogen heat hybridization hydrocarbons hydrogen halides hydrolysis hydroxide hydroxyl iodide isomers IUPAC name kcal/mol ketone kJ/mol lithium mechanism methyl methyl group molecular formula molecular models molecule nitrogen NMR spectrum nucleophilic substitution orbital oxidation oxygen phenol prepared primary PROBLEM propene proton react reaction reactive resonance ring SAMPLE SOLUTION secondary Section sodium stable step stereogenic center stereoisomers structural formulas synthesis tert-butyl tertiary tetrahedral intermediate tion yield