e to see the electron pushing mechanism drawn out Propose an electron-pushing mechanism for the following reactions. 1. + 2 H₂O d-limonene H* OH OH la НО. terpin OH lb
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- Complete the following reactions: CH, CH, ROOR hv H₂O, HgSO H₂SO4 1 mole of HBr alcoholic AgNO, major organic product enol product (5) major organic product major organic product (3) process 1 mole of HBr keto product (6) major organic productDraw the structure of the product/s in each of the following reactions. CuBr NaNO2, HCI, H,O, 0°C (F) (G) Para-methyl- aniline KI CUCN OH- (H) (), (J) phenolThe key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold Helminthosporium sativum, involves the following base treatment of a keto tosylate. What kind of reaction is occurring? How would you complete the synthesis?
- A hydrocarbon of unknown structure has the formula C8H10. On catalytic hydrogenation over the Lindlar catalyst, 1 equivalent of Η2 is absorbed. On hydrogenation overa palladium catalyst, 3 equivalents of Η2 are absorbed. (a) How many degrees of unsaturation are present in the unknown structure? (b) How many triple bonds are Present? (c) How many double bonds are present? (d) How many rings are present? (e) Draw a structure that fits the data.The conversion of 3 alcohols into alkenes under acidic conditions involves two cationic intermediates. For each reaction, draw the complete mechanism using curved arrows.Draw the major organic product for the reaction at -78 °C: Select Dr 1. Li*[AIH(OtBu)3l CI 2. H20
- ) draw the arrow-pushing mechanism of the following reaction: OH H,SO4What reagents are necessary to perform the following reaction? HO, CI Multiple Choice CH3CH2NH2, DCC SOCII2 Heat ELOH, H*Diaw structural formulas for the major organic producto 9) MCH SOCI₂ b) 2) d) SE охон a OH HCl OH HBr excess H₂ CrOA HIOA DOD4, HD₂ HIO pruch, THEO 2) ft₂N for each reaction.
- What reaction took place in the reaction below? CHẠCH, CH; CH,(CH),CH; CH{CH,),C-OCH; CHẠCH)A CH; CHỊCHCo H0 НОСН CH/CH),CH, CH, (CH),C-C HOCH, HH O reduction (hydrogenation) O amide synthesis O acetal hydrolysis O ester synthesis O acid base O dehydration O thioester synthesis O phosphate ester synthesis O hydration O ester hydrolysis O amide hydrolysis O oxidation O acetal synthesisDraw Intermediate CH3OH₂+ protonation H H3C -0 H Q CH3OH deprotonation loss of H₂O elimination H3C :0 ÖH -CH3 Draw Intermediate CH3OH deprotonatio Please select a drawing or reag36) Draw the major product of the following reaction: 1. BH3 2. H₂O₂, OH