4. Draw the mechanism of the reaction between toluene and isopropyl chloride in the presence of...
· Draw the mechanism of the reaction between toluene and isopropyl chloride in the presence of AlCl3 to give 4-isopropyl toluene. (7 points) CI AICI: +
3. Please indicate how many pi electrons each of the following compounds have and whether they are aromatic, non-aromatic, or anti-aromatic. (8 points) 4. Draw the mechanism of the reaction between toluene and isopropyl chloride in the presence of AlCl3 to give 4-isopropyl toluene. (7 points) AICI: Please draw the major product or products of each of the following reactions. (4 points each) HBr/ UV light 5. Brą/UV light
Draw the product of the following reaction between toluene and 2,4-dichloro-2,4-dimethylpentane in the presence of AlCl3 Draw the product of the following reaction between toluene and 2,4-dichloro-2,4-dimethylpentane in the presence of AlCl3
5) When benzene reacts with isopropyl chloride in the presence of AlCl3, a compound with a molecular mass of 162 g/mol is isolated. In HNMR, this compound has the following spectrum. What is it and why is it formed? PPM
Predict the product(s) for the reaction of toluene with propanol bromide in the presence of aluminum bromide catalyst; what is the name of this reaction? Draw the mechanism of the formation of the major product. Consider whether an additional substitution will take place and at which position. Consider whether an additional substitution will take place and at which position. Consider what would be different if bromine was used in the presence of the same catalyst.
C12H14O3 + Toluene/AlCl3 = C19H22O3 Provide detailed structures and mechanism with arrows for the above reaction.
Draw the product and mechanism of the following Friedel-Crafts reaction. 4. Draw the product for the following reaction. Hint: Draw the mechanism for the electrophile formation first. AICI: Followed by workup
12. In a synthesis of isopropyl pyridine, the 3-methyl-2- presence of sodium ethoxide to give a dicarbonyl compo NaOCH.CH opropyl pyridine, the 3 with ethyl formate in the 0 ethyl formate 3-methyl-2-butanone a) In the first step of the mechanism, sodiu alpha position to form an enolate. Complete the as necessary (4 points) step of the mechanism, sodium ethoxide deprotonates 3-methyl-2-buthone at the O form an enolate, Complete this reaction with curly arrows drawing in H atoms b) Why is...
Draw the mechanism for the following reaction: AlCl3 Draw the mechanism for the nitration of benzene.
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! :)