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- Complete the reactions belowDraw the reactant of the following reaction sequence.THE MECHANISM: Step 1: In aqueous acid, the first step is proton transfer to the carbon-carbon double bond. H BOH H Hydronium ion RCH₂ R' Conjugate acid of ketone 1-Hexyne draw structure... +RCH= SÖH Enol Step 2: The conjugate acid of the ketone transfers a proton from oxygen to a water molecule, yielding a ketone. ¹H- H + :0: R' H Water H :O: +RCH- H Water 1. R'₂BH 2. H₂O₂, NaOH RCH₂ Ketone R' R' H Conjugate acid of ketone +ÖH + Hexanal H H-O: H Hydronium ion H
- A useful way to synthesize alkaloids is called the Pictet-Spengler synthesis. The first two steps of the synthesis are shown below. The first step involves a nucleophilic attack, and the second step is a typical elimination reaction. Provide a reasonable mechanism using curved arrows for both reactions.Predict the major product of the reaction and draw it in the space provided. + HN. NPh NaBH3CN MeOH/ACOHa) provide the name of each compound in the reaction above, underneath the structure. b) Provide the mechanism of the transformation below. HOH HOH HO CH3OH HO HO HO H -OH H. -OMe H OH cat. HCI OH H OH H
- Do the reactions below proceed in good yield from left to right as shown? a) yes no b) no ii 1 equivalent OH + HO & - OCH 3 Ol sl Na O OH NaOH H₂O HO تمليك حملی + stol + Na O Na OCH3help with the questions except number 1Complete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible answer. 1) CH3CH2M9B CH3OH H+ (ехcess) но 2) H30*, H2O B A OCH3
- Predict the product for the following reaction. 1. Br₂/H₂O 2. NaOH OH Br Br Br OH ميد مير يد سيد IV || OIVComplete the mechanism for the base-catalyzed opening of the epoxide below by adding any missing atoms, bonds, charges, nonbonding electron pairs, and curved arrows. -CH3 -CHз Нзс—ӧ: :0-CH3 :ÖH НзС—0:Provide an arrow pushing mechanism for the following reaction. Include protons and each step clearly indicated. Br H. D H3C Hz H3C CH3