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- 4-chloro-4- isopropyl-3-butanone 1 - chloro-1 - isopropyl-2 - butanone 3- chloro-2-methyl-4 - hexanone 4 - chloro-5-methyl-3 - hexanone methyl-4- cyclohexanoneProvide the reagents necessary to complete the following transformation. CH, -CH3 OHNonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated , -unsaturated isomers. Propose a mechanism for this isomerization.
- need help with providing a good reagentRank the compounds in each group in order of increasing reactivity in nucleophilic acyl substitution. C6H5CO2CH3, C6H5COCl, C6H5CONH2Match each reagent to the product that it forms. Multiple reagents may form the same product. нох Reagent Reagents SOCI2, pyridine: C CISO2CH3, pyridine: E HCI: A PCI 3: A A) B) "It "ft "bl H₂O D) E) F) پہلے علی علیہ
- Draw the major product(s) when the following molecule is reacted with excess NaOEt in EtOH, followed by aqueous acidic work-up. CH;CH,OĊCH(CH,)¿COCH,CH3 CHaO -NHCCH3 CH₂CH3 ELECTROPHILIC AROMATIC SUBSTITUTION IN ARYLAMINES CH3C O - NHCCH3 0 CH₂CH3Draw the major organic product for the reaction conditions shown. CH3 mCPBA CF3SO3H CH₂Cl₂