When drawing the product, keep the NO2 group on top of the benzene ring (under the COOH tool, there is an NO2 substituent button). When drawing the product, keep the NO2 group on.ĭraw the product of the following reaction. Draw the product of the following reaction.Separate resonance structures using the symbol from the drop-down menu. Add additional sketchers using the drop-down menu in the bottom right comer. For structures having different hydrogens of comparable acidity, assume that the reaction occurs at the less-substituted carbon. (References H Include all valence lone pairs in your answer. (Review Topics Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of the compound below with base. (Review Topics Draw both resonance structures of the anion formed by the reaction of the most. #CHEMDOODLE DELOCALIZED BENZENE ACTIVATOR#Explain why- NH2 act as an activator and. While a methoxy group is strong activating. Explain why a methyl group is a mildly activating group You identify some of the relative rates of reactivity? Why does performing the experiment at 0 degrees Celsius help Include the resonance structures for any charged,ĭelocalized intermediates that are involved. Reaction mechanism for the bromination of acetanilide to create the Using curved arrows to symbolize electrons, write a complete Reaction mechanism for the bromination of. Explain using the resonance structures (referred to as the "sigma complex") why the. Use your pre-lab lecture notes to answer this question. Given that a methoxy (-OCH_3) group attached to the benzene ring serves as an orthopara director, draw the major products of the reaction shown below. We saw in this experiment that an ester group with the carbonyl carbon attached to the benzene ring serves as a meta-director, resulting in methyl Meta-nitrobenzoate as the major product of the reaction.
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