Propose an efficient synthesis for the following transformation: The transformation above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. A. t-BuOK B. 1) n-PrMgBr; 2) H3O+ D. RCO 3H G. NaOEt OH FGDE E. 1) EtMgBr; 2) H3O+ H. 1) n-BuMgBr; 2) H3O+ C. 1) LIAIH4; 2) H3O+ F. NBS, heat I. 1) 03; 2) DMS

Draw the full electron pushing mechanism for the reaction depicted including ALL intermediates (with lone pairs and formal charges). Clearly label the electrophile and nucleophile in each step where appropriate.

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plz.answer if you r 100% with proper explanation.

in addition also is it aromatic non aromatic or anti aromatic

Part A Provide the major organic product. H H HOI Draw the molecule on the canvas by choosing buttons from the Tools (for toolbars. The single bond is active by default. G

Circle the molecule that will undergo electophilic aromatic substitution at a faster rate

Please help, with explanation need

Give a clear handwritten answer with explanation ..give Detailed answer of given reactions....give answer all sub parts

Label each heterocycle as aromatic, antiaromatic, or not aromatic.