3. Propose a synthesis for the following transformation. Do not draw an arrow-pushing mechanism below, but make sure to draw the product of each proposed step (3 points). + En CN CN
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- 4. Propose a plausible synthesis for each of the following transformations. Don't show mechanism. Only provide the necessary reagent(s) and products for each step. a) „Ó -d b) OH HO Br میں کچھDraw the major product of the following reaction sequence. OH H2CrO4 HO NaBH4 H*/H20 ELOH он H3C* ноprovide a synthesis for the following molecule. Starting materials are shown in the left hand side. You don't need to show the mechanism, just show the needed reagents and DO NOT skip any step
- Draw the major product formed for each reaction. Assume the reactions are irreversible. Include stereochemistry when products contain stereocenter(s). It may be helpful to first identify whether the reaction is a substitution (and SN1 or SN2), an elimination (and E1 or E2) or a carbonyl addition. (a) 1 equiv means for every molecule of substrate, there is one molecule of NaOCH3 Br Br NaOCH 3 (1 equiv) 0 °C (b) Draw only the substitution product. Both elimination and substitution occur here. (၁) CH3 Br Br CH3OH NaOCH3 80 °C (d) "Then" means CHзl is added after the Grignard reacts. H3C MgBr (1 equiv) then CH3lDraw the products formed after Steps [1] and [2] in the following threestep sequence. Then draw stepwise mechanisms for each step.1) Please draw the mechanism for the following transformation. OH Br
- Please use appropriate reagent to transform the following . GIVE REASON FOR USING A PARTICULAR REAGENT AND MUST GIVE MECHANISM PLZ . DO NOT SKIP MECHANISM. DO ALL , PLZ DO NOT COPY FROM CHEGG if you plan to do only 1 then skip lets some other do allPropose an efficient synthesis for the follwoing transformation. You may use any reagent you need. You do need to show mechanism and products for each individual reaction.epi-Artistolochene, a hydrocarbon found in both pepper and tabacco, is biologically synthesized by the follwing pathway. Add curved arrows to show the mechanism of each step