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- To preview image click here Perform the retrosynthetic analysis for the indicated bond and choose the correct synthetic equivalents. A. B. OA B Oc OD :0: O= H H :0: H + Na C. +Na H- 0: D. + Na H + +NaProvide the reactants that would give the following aldol condensation product. ہولی ہولی من ہے تو جو A. H B. .H C. D. .H HKindly draw the product that was fromed when phenylacetic acid was treated with the reagent, show the process and give some explanation. Thanks! a. [1] SOCI2; [2] CH3CH2CH2NH2 (excess) b. [1] SOCI2; [2] (CH3)2CHOH
- Provide the reactants that would give the following aldol condensation product. ... H + A. له شوه B. مله .H .. C. D. HTo preview image click here ↓ Perform the retrosynthetic analysis for the indicated bond and choose the correct synthetic equivalents. A. B. O A B D : OMe + :0: + NaOMe + NaOMe C. D. MeO +ÖMe + NaOH NaOHThe methoxy group (-OCH3) group is considered a .... Ortho/Para Directing Activator Ortho/Para Directing Deactivator Meta Directing Deactivator
- 1. a. Somtimes cyanides can by useful functional groups, but not in a way that we would typically think about them. Promide a mechanism for the following transformations and provide the structure of A. LDA, THF, O *C: NaH, THF, O "C; A then add then Br OMe Meo CN b. Sometimes Aldol-type products can be forged in non-canonical ways. Provide a mechanism for the following transformations. When necessary, depict all proton transfors. H,O, NaOH catalytic KCN OH Ph THFH,O Ph Меон Ph OMeI'm stuck on the last part, what happens after acylation since we don't have any of the reagents to leave, and NH2 is not one of course. what is D? explain please3. Propose your own synthesis of compound C. HHOH readily available precursors
- 2. When the following pair of reactants are combined in the presence of a basic catalyst, a number of aldol addition products are possible (since both of the reactants possess an acidic alpha proton). a. b. C. CH3 + H₂C H NaOH/H₂O Draw the structures for the two possible enolate ions. Draw the structures for all possible aldol addition products (also show the enolate ion and electrophilic carbonyl compound responsible for each product). For each of the aldol addition products predicted in part b, draw the structures for all of the corresponding aldol condensation products after loss of water (if E/Z isomers are possible, show both isomers)Draw the complete mechanism for the tautomerization of 3-butanone under... ОН a. Acidic conditions (H3O*, H2O) b. Basic conditions (NaOH, H2O)2. Design a synthesis of Compound G from Compound F (more than one step is required)? HO Compound F Compound G