CHEM 2320 Lecture Notes - Lecture 19: Kodak Gallery, Acid Dissociation Constant, Fluorine
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25 Feb 2017
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Behzylic process . oxidation strong agent lose carbon. Need in would acid basic because conditions. H2cro4 there needs to be a hydrogen at the blnzylic position for this reaction to take place. %0h o get a dicarboxylic acid acid anhydride. For a given mono substituted benzene how does reactivity compare to benzene. Ortho , meta , or para ? assuming. 4 f- on the electron less nudeophilic benzene less reactive making mating group more more nudeophilic reactive. G %withdrawing already a group there directing ability depending group. Ewg . effects inductive resonance epa weak e donating group. Aniline is a stronger electron donating group because the amide has a competing resonance out to the. They sit on the fence ; in terms of resonance. Inductive effect ( ewg ) is stronger as far as activating or deactivating weak. Alkyl groups donate electron density to carbo cations and make them more stable. Substituent effects on benzene reactivity towards electhphilic substitution.
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