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![5.
How would you prepare the following ketones/aldehydes using an acetoacetic or
malonate synthesis? Give the starting materials.
CH3
CHO
H3CC
OHC](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fcd7e28f7-50c6-45d1-a2f5-3cbb047b8845%2Fdabceee5-c028-4f0b-8f39-8468a21d82b6%2Fzp03ck9_processed.jpeg&w=3840&q=75)
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- Draw the major product(s) for reaction of methyl pentanoate with: NaOH, H2O, heat; then H3o*9) How would you carry out the following transformation? More than one step may be required, write the reactions. H3C CH 3 H3C ? H3C CH3 OH H H3C H "ОН 10) How would you synthesize the following compound from cyclohexanone? More than one step may be required, write the reactions. CH 3Question 9 The reagent which converts a carbonyl group of a ketone into a enamine group is O CH3CH2CH2NHCH3; H CH3CH2CH2NH2; H* O CH3CH2CH2NHCH3; H3O* O CH3CH2CH2NH2; OH OLIAIH[OC(CH3)3]3
- Complete the given reactions by drawing the structures of the major organic products: Please draw the completed reaction OH HO HOCN H₂N H₂O H3PO4 OH HO HO. (excess) H3O+ H2SO4 H*Provide the major organic product of the following reaction. but-1-yne 1) Sia₂BH 2) H₂O₂, OH What is it called when an enol converts to a keto? A) Keto-enol isomerism B) Keto-enol tater tot-ism C) Keto-enol conversion D) Keto-enol tautomerismhow to synthesize 2-phenylclohexanone from cyclohexanone?
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