2. Propose reagents for reducing the following carbonyl compounds: [7 x 2] 요? a) i Chemistry Steps ?2 Chemistry Steps OH Che b) c) d) Chemistry Steps CO Chemistry Steps OH OEt ? co Chemistry Steps ? CO OH H A Che ? mistry Steps Che e) f) CO Chemistry Step Cher 요 CI ? CO Chemistry Steps CO ? Chemistry St Che OH H
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- What carbonyl compounds might you start with to prepare the Following compounds by Grignard reaction? List all possibilities. (a) 2-Methyl-2-propanol (b) 1-Ethylcyclohexanol (c) 3-Phenyl-3-pentanol (d) 2-Phenyl-2-pentanolFill in the missing reagents a-h in the following scheme:Draw the organic product formed for each reaction. e. CI & COOH COOHfallization of A COOH [1] LDA [2] CH3CH₂I [1] Br₂, CH3CO₂H [2] Li₂CO3, LiBr, DMF 1₂ (excess) TOH -aminopher should you use NaHnimm CN to the Büchn Br₂ (excess) -OH ydride to form ace + CHI3 rinse the task wh
- Multi-step synthesis: Provide reagents needed for the following transformations. More than ne step is rquired for each reaction.dedcue the major organic product from the following reations. be ablw to draw hydration halogenation hydrohalogenation, halohydrin formation, oxymercuratiom demercuration qnd hydroboration oxidation.Choose the best reagents to complete the following reaction. Option E is (CH2OH)2, TSOH (Please show reaekson and don't use hend raiting please)
- 1.Draw the structures of all 3 resonance hybrid forms of the benzenonium intermediatefor both o and p attack for the case of activating groups an indicate which one in eachcase is the most stable form.Draw the structure of all 3 resonance hybrid forms of the benzenonium intermediatefor m attack in the case involving a deactivating group. 2.Halogens are deactivating groups but direct electrophilic attack at the o and ppositions. Why is this the case?Why does the alpha hydrogen to a ketone have a lower pka value than the alpha h to an alkene. Draw a picture to explain ur a waysthe reagents are LiAlH4 Et2O / H2O, can you please redo with these reagents? Thank you.
- 15.3 (ghi) Predict the the major product or reagent that completes the transformationUsing chair confirmations, draw the final product of each molecule. Pls explain how are you arrived at the answerthank you!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.