CH37 H2SO4 CH3 от .A) Provide a complete mechanism for the above Friedel-Crafts Reaction. Pay close attention to details, including lone pairs, formal charges and the use of curved arrows.
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- ! ( give step by step explanation)The above reaction involves heterolytic bond breakage of HBr a) Encircle the nucleophile (s) and electrophile (s) and explain why. b) Give the mechanism of the reaction by: ) Drawing the appropriate arrows to track the flow of electrons in Showing the species formed after bond breakage and bond formation with appropriate charges. c) Predict the final products.3c）Referring to the intermediates you drew in problem below explain in detail why no meta product is obtained in the Friedel-Crafts alkylation of chlorobenzene. Draw all pertinent resonance structures to support your argument.
- Draw the structure for each of the following molecules. (a) 1,3-divinylcyclohexane; (b) 3-allyl-4-vinylcyclopentene;(c) dimethylacetylene; (d) divinyl ether; (e) 4-vinylocta-1,3,7-triene; (f) 2-allylcyclohexa-1,3-dieneWhen piperidine undergoes the series of reactions shown here, 1,4-pentadiene is obtained as the product. When the four different methyl- substituted piperidines undergo the same series of reactions, each forms a different diene: 1,5-hexadiene; 1,4-pentadiene; 2-methyl-1,4-pentadiene; and 3-methyl-1,4-pentadiene. Which methyl-substituted piperidine forms which diene?Represent a structure of product A (bicyclic molecule) and propose a detailed mechanism for its preparation.
- Draw an arrow-pushing mechanism for the reaction below. Include all formal charges and lone pairs.Provide the complete mechanism for the reaction. Please include appropriate arrows, intermediates, and formal charges.Provide a complete mechanism for the reaction, including all lone pairs, formal charges, andcurved arrows.
- for this mechanism, show all steps including resonance structures and intermediates. thank you!Please provide a mechanism (including all relevant resonance forms of the intermediate)The following reaction is Friedel-Crafts alkylation. Considering the mechanism for Friedel-Crafts alkylation, how would you explain the formation of this particular product? Either describe or upload image of the mechanism. AICI,