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- provide the mechanism! The tautomer that predominates in aqueous solution A. Enol B. Keto form4. Draw the final major product(s) for each multistep synthesis reaction. H3O* OMe H3PO4 Jones Et,NH reagent H30* PBR3 KOC(CH3)3 1. O3 NABH3CN HO- 2. DMS NH3, H3O* Br KOC(CH3)3 1. ВНз PCC H3O* 2. H2О2, ОН CH2CI2Draw the alkyl bromide for reaction 2. Select Draw Rings More Erase | 7 | | H Br Reagents Carboxylic Acid Product 1. Diethyl malonate, NaOC2H5, C2H5OH 2. NaOH, H2O 3. H3O*, heat ОН Draw the alkyl bromide for reaction 3.
- Alkyl diazonium salts (shown below) are considered "super" leaving groups; a consequence of this is that they tend to be contact explosives What quailities make alkyl diazonium salts such excellent leaving groups?finish these to given parts of the reaction then give the final proGive detailed Solution with explanation needed
- can you please help mePredict the product of the reaction shown and complete the curved-arrow mechanism for its formation. (Hint: Friedal- Crafts alkylations can be used to form rings.) AICI, → a compound C,H2 + HCI PHCH,CH,CH,CH,CI- Step 1: Draw one curved arrow. Step 2: Complete the structure, then draw curved arrows for the EAS reaction. Select Draw Rings More Erase Select DrawRings More Erase H Al Cl H Al Cl : C : Al : d :This reaction is an example of conjugate addition of a nucleophile to an a,ẞ-unsaturated carbonyl. O CH3CH2CH2CH=CHCSCOA H₂O OH CH3CH2CH2CHCH2CSCOA Draw the two resonance structures of the enolate anion intermediate for this reaction. • Draw an R1 group in place of COA. The R group tool is located in the charges and lone pairs drop-down menu. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate resonance structures using the symbol from the drop-down menu. ->> 90-87 O + ? ChemDoodle >



