Show mechanism and product for each of the following. In any aldol reactions, be sure to show any possible E1cb reaction; in any decarboxylations, be sure to show the correct orientation. 2 人 NaOH CHO H₂O
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- Part 3 Complete the mechanism for the reaction. Mild Acid Draw the mechanism arrows. yh y X See HintPropose a complete mechanism for the following reaction and draw each step in the mechanism. но H;O* OH +Draw the structure of the major aldol product (prior to possible dehydration) of the following reaction without specifying stereochemistry. CH3 ལན། ཚིགས་. dilute aqueous NaOH 0-5° You do not have to consider stereochemistry. If no reaction occurs, draw the organic starting material. 0 + ChemDoodle [] за
- show all steps and use the arrows correctly. Propose a mechanism that explains the product for the following reaction. Be sure to ILO H₂SO, OH Xo4. Tertiary amines undergo reversible conjugate additions to a,ß-unsaturated carbonyls. The reaction shown below uses this phenomenon followed by an aldol-like process to obtain the given product. Show a detailed mechanism for this reaction. The structure of one of the intermediates is shown below to assist in drawing the mechanism ОН О Ph + Ph H. H2O/E1OH ОН О intermediate: Phi `NMe3The reaction shown below proceeds by both an SN1 and an SN2 mechanism. Draw the products of each process and use mechanistic arguments to account for any differences in the products formed. Ph 'Br SH Base
- For the following reaction predict the major product and draw the complete mechanism including the mechanism for the electrophile formation. CF 3 H₂SO4 HNO34) Show a detailed mechanism for the following transformation. OH OH OH HO HO -H OH CH₂OH HCI HO HO. OH -H OHI SOCH 3 HO -OCH 3 OHI HWhat is the product of the following sequence of reactions? D | NaOH NaNH2 H3O+ || ||| explain each steps..explanation needed. don't give Handwritten answer IV NH₂
- Draw the structure of the major aldol product (prior to possible dehydration) of the following reaction. O ⇐ H dilute NaOH 95% aq. ethanol, 0-5° • You do not have to consider stereochemistry. •If no reaction occurs, draw the organic starting material. + HO CH3 On t ?When the ketone and aldehyde shown below are treated with a base two possible products are formed. Discuss how each product is formed and provide a mechanism.Draw the structure of the major aldol product (prior to possible dehydration) of the following reaction. CH3 CH3 H dilute NaOH 95% aq. ethanol, 0-5⁰ You do not have to consider stereochemistry. • If no reaction occurs, draw the organic starting material. O-Sn [F ? ChemDoodleⓇ