how to get 1-(1-methyl-3,4-dihydro-1H-isoquinolin-2-yl)ethanone from N-ethenyl-N-(2-phenylethyl)acetamide . answer and explain it step by step
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how to get 1-(1-methyl-3,4-dihydro-1H-isoquinolin-2-yl)ethanone from N-ethenyl-N-(2-phenylethyl)acetamide .
answer and explain it step by step
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- how to get 1-(1-methyl-3,4-dihydro-1H-isoquinolin-2-yl)ethanone from N-ethenyl-N-(2-phenylethyl)acetamide answer this step by stepp-Nitrobenzaldehyde is more reactive toward nucleophilic additions than p-methoxybenzaldehyde. Explain.Show how to convert (R)-2-pentanol to (S)-2-pentanethiol via a tosylate. SH (R)-2-Pentanol (S)-2-Pentanethiol
- What main signals would you expect in the IR spectrum and in the NMR spectrum for 3- (4- (dimethylamino) phenyl) -3-hydroxy-1- (p-tolyl) propan-1-one?how to synthesize 2-phenylclohexanone from cyclohexanone?Reaction of p-nitroaniline with sodium nitrite and hydrochloric acid at 0°C, followed by treatment with N,N-diethylaniline.
- 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) propanone1) Draw AND name the product that would result upon treatment of R-3-methylheptanal with Excess aqueous sodium hydroxide together with excess chlorine. 2) Draw AND name the product that would result upon treatment of R-3-methylheptanal with Bromine in acetic acid. 3) Draw the product that would result upon treatment of R-3-methylheptanal with1-butanamine using a Dean Stark trap. Draw the product and then react the product with lithium aluminum hydride followed by hydrochloric acid. Give a complete mechanism. 4) Draw the product that would result upon treatment of R-3-methylheptanal with Disopropyl amine using a Dean Stark trap. Draw the product and then react the product with hydrogen gas in the presence of a platinum catalyst.3,5-Dibromo-4-hydroxybenzenesulfonic acid is used as a disinfectant. Propose a synthesis of this compound from phenol.
- Can you please explain why treatment of 1,4-dihydronaphthalene even a trace of acid results in the formation of 1,2-dihydronaphthalene? I can’t understand it’s mechanism.The fragrance of (Z)-1-phenylhex-2-en-1-ol resembles that of roses, with a delicate citrus edge. Show how you would synthesize this compound from benzaldehyde (PhCHO) and any other reagents you need.What is the systematic name of: 1) 2-(1-hydroxypropyl)-6-isobutylcyclohexan one 2) 2-(diethylamino)-N-(2,6-dimethylphenyl)acetamide OR 2-N,N-diethylamino-N-(2,6-dimethylphenyl)-ethanamide 3) N-(3-(trifluoromethyl)phenyl)-2-aminobenzoic acid 4) (E)-1,2-bis(2,4,6-trinitrophenyl)ethene 5) 5-choloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide 6) 4-isobutyl,3-N-ethyl amino phenol 7) 1-bromo,2-(N-ethyl,N-methyl)amino,3-thiol pentanone