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- Why can’t 1-methylcyclohexanol be prepared from a carbonyl compound by reduction?how to synthesize 2-phenylclohexanone from cyclohexanone?Propose a mechanism for the reaction of benzyl acetate with methylamine. Label theattacking nucleophile and the leaving group, and draw the transition state in which theleaving group leaves.
- Describe how 3-methyl-1-phenyl-3-pentanol can be prepared from benzene. You can use any inorganic reagents and solvents, and any organic reagents provided they contain no more than two carbons.Draw out the reaction mechanism for cyclohexanol to cyclohexanone. Sodium hypochlorite oxidation of an alcohol to a ketone with the product being cyclohexanone.The product of reaction between formaldehyde with 2-methyl propanal give 2,2-dimethyl-3-hydroxy propanal 2,2-dimethyl-3-hydroxy propanone 2,2-dimethyl-3-hydroxy propanoic acid 2,2-dimethyl-3-hydroxy propanol 4-phenyl-3-buten-2-one prepared from reaction between Benzaldehyde with acetic acid Benzaldehyde with acetaldehyde Benzaldehyde with formaldehyde Benzaldehyde with acetone Which predict product for reaction between heptane-6-one-1-al with sodium hydroxide * 1-(2-hydroxycyclopentyl) pentanone 1-(2-hydroxycyclopentyl) butanone 1-(2-hydroxycyclopentyl) ethanone 1-(2-hydroxycyclopentyl) propanone
- Write an equation for the reaction (if any) of benzaldehyde with each of the following reagents: - a) Tollen's reagent b) hydroxylamine c) ethyl magnesium bromide, then H3O+ d) phenylhydrazine e) HCN f) excess methanol, H+ g) LiAlH4 h) ethylene glycol, H+Find the product formed in:a) Heating benzene diazonium chlorideb) Sodium benzene sulphonate with NaOHWhat product will be formed on reaction of propanal with 2-methylpropanal in the presence of NaOH? What products will be formed? Write the name of the reaction also.
- 1. Propose a mechanism to account for the formation of 2,3-dimethyl-2-butene from 3,3-dimethyl-2-butanol b. Propose a mechanism to account for the formation of 1,2-dimethylcyclohexene fromthe acid-catalyzed dehydration of 2,2-dimethylcyclohexanolWhat steps are needed to convert benzene into p-isobutylacetophenone, a synthetic intermediate used in the synthesis of the anti-inammatory agent ibuprofen.Explain why pentane-2,4-dione forms two alkylation products (A and B) when the number ofequivalents of base is increased from one to two.
