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Draw the two step mechanism for the nitration of bromobenze to give the para product. Draw...
In nitration of acetanilide(synthesis of p-nitroaniline) main product is ortho and para. Explain why ortho and para product is major in resonance and mechanism term.
Write a mechanism for the nitration of methyl benzoate (major product only) Include formation of the electrophile from the reaction of nitric acid with sulfuric acid. Only one resonance structure is needed for the intermediate in the EAS portion of the mechanism
Draw the mechanism for nitration of phenylacetic acid. Include formation of the electrophile. The mechanism should explain why the product is ortho, para, or meta
8. Propose a mechanism for the nitration of anisole to give ortho and para nitroanisole. (10 pts) OCH HNO3 H2SO4
For the nitration of methyl benzoate, draw the sigma complex (the reactive intermediate) which results from attack at the ortho, the meta, and the para positions. For each sigma complex, draw all appropriate resonance structures. Circle any "high energy'' resonance structures.
Draw the reaction mechanism of phenol nitration, show the ortho and para mechanisms separately. Include arrows, eletron flow and lone pairs.
The nitration equation and mechanism of bromobenzene. Also, would the final product be para, orthodontist, or meta? 4 mL conc. HNO3 4 mL conc. H2SO4 1.5 mL or bromobenzene
4. (5 pts) Draw a complete, step by step mechanism to account for the formation of following product. Draw all the resonance structures of the intermediate and indicate which one is the major resonance contributor. осна OCH3 Br2 FeBr3
Provide a mechanism that explains formation of the following products. Draw step 1 of this mechanism. Include lone pairs and formal charges in the mechanism. Draw out explicitly only the hydrogen of the H_3O^+. Draw step 2 of this mechanism. Include all lone pairs and formal charges in the mechanism. Do NOT draw out any hydrogen explicitly. The product of the above mechanism step has a resonance structure that leads to the formation of the second product. Draw the resonance...
Draw the structure of the product of each step in the following three-step synthesis. If a nitro group is in the structure, use the functional group tool to put it in, do not draw it out (i.e. put in NO2). Although the first step produces a mixture of isomers, the para isomer is isolated as the sole product of interest and used in the second step. Give only the major product for the second and third steps. HNO Brz Br2...