Draw the mechanism for the following reaction: AlCl3 Draw the mechanism for the nitration of benzene.
The first reaction for the mechanism for the nitration of benzene is: O A. Nitric Acid + Nitric Acid O B. Benzene + NO2 C. Nitric Acid + Sulfuric Acid OD. Benzene + NO2+
Use a sheet of paper to answer the following question. Draw the mechanism for the nitration of benzene using a mixture of nitric and sulfuric acids.
Give the product of the reaction of excess benzene with isobutyl chloride + AlCl3. Please draw out the full picture to receive Lifesaver rating and thank you much! :)
4. Draw the mechanism for the reaction of benzene with Et and base. 5. Draw the mechanism for the reaction of propanal with CN/HCN. ... unalauda in the correct acometry showing its orbitals
Question 9 Identify the electrophile in the nitration of benzene reaction. a) NO2+ b) NO3+ c) NO2 d) HNO3 Question 10 Which of the marked hydrogens is most acidic?
Identify the correct reagent for the following reaction: (1 point) Conversion of Benzene to Acetophenone Chloroethane-AlCl3 b) Acetylchloride-AlCl3 c) Acetaldehyde-AlCl3 d) Acetic acid-NaOH
9. What product is formed when benzene reacts with AlCl3 and each of the following reagents? 10. Draw all the products of the following reaction: + OH
Draw the reaction mechanism of phenol nitration, show the ortho and para mechanisms separately. Include arrows, eletron flow and lone pairs.
Design a scheme and draw the mechanism for the synthesis of the following compound from benzene and an alkyl halide. Application Questions 1. Design a scheme and draw the mechanism for the synthesis of the following compound from benzene and an alkyl halide. For the compound in application question one, design a scheme and draw the mechanism for the synthesis from benzene and an alcohol. 2. Explain why you cannot directly form the following compound from a Friedel-Crafts alkylation of...
Draw the reaction mechanism for the nitration of methyl benzoate to methyl nitrobenzoate, please show all resonance structures for each possible substitution position to explain why methyl m-nitrobenzoate was the favored isomer.