view - Topic 16.7 Addition of Oxygen Nucleophiles 16.8...

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Topic Comments 16.7 Addition of Oxygen Nucleophiles Hydrates; hemi-acetal; acetal formation; acetal protecting group; mechanisms 16.8 Addition of Nitrogen Nucleophiles imines and enamines-formation and hydrolysis; mechanism 16.9 Keto-Enol Tautomerism acidity of α hydrogens (significance); mechanism-acidic & basic 16.10 Oxidation +6 reagents; Silver oxide;O 2 16.11 Reduction metal hydride reductions; mechanism; cat H 2 ; Clemmenson; Wolff-Kishner 16.12 Reactions at an α -Carbon Key Reactions 17 Carboxylic Acids 17.1 Structure 17.2 Nomenclature trivial names of compounds on slides; basic nomenclature, otherwise 17.3 Physical Properties solubility trends; BP & or MP trends; spectral properties 17.4 Acidity pKa values & use; stability of anions; equilibrium 17.5 Preparation of Carboxylic Acids Grignard route-oxidations 17.6 Reduction LAH; selectivity of reductions 17.7 Esterification Fisher esterification-mechanism; Diazomethane 17.8 Conversion to Acid Chlorides
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view - Topic 16.7 Addition of Oxygen Nucleophiles 16.8...

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