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Organic Chemistry Structures of Organic Compounds

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3 o Alcoholno reaction at normal temps, No H-COH to oxidize!Aldehydes and KetonesPreparationOxidation <strong>of</strong> 1 o Alcohol (15)HOH+ PCC CH 2Cl 2HO2-methylpropanol2-methylpropanalOxidation <strong>of</strong> 2 o Alcohol (15)H+ KMnO 4OOH3-methyl-2-butanol3-methyl-2-butanoneReactions <strong>of</strong> Aldehydes and KetonesNucleophilic AdditionThe carbon in C=O is electron-poor, an electrophile.δ+ δ-Oδ-X δ+YXORO Y +ionicXOYcovalent

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