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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 .
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- what is major product of following Benzaldehyde--- NaOH ----propanal ----->? ( a ) α-hydroxy-2-methyl-3-phenyl propanal ( b ) β-hydroxy-2-methyl-3-phenyl butanal ( c ) β-hydroxy-2-methyl-2-phenyl propanal ( d ) β-hydroxy-2-methyl-3-phenyl propanal (e ) ɷ-hydroxy-2-methyl-3-phenyl propanalhow 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 step1-Draw the mechanism of 1-methylcyclohexene with hydrogen bromide please. 2-Draw the reaction mechanism METHYL MAGNESIUM BROMIDE with PROPANAL and PROPANONE please.
- 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.What product result from nitration of benzaldehyde ?p-Nitrobenzaldehyde is more reactive toward nucleophilic additions than p-methoxybenzaldehyde. Explain.
- 2-Pentylcinnamaldehyde, commonly called flosal, is a perfume ingredient with a jasminelike odor. Flosal is an α,β-unsaturated aldehyde made by a crossed aldol reaction between benzaldehyde (C6H5CHO) and heptanal (CH3CH2CH2CH2CH2CH2CHO), followed by dehydration. Draw a stepwise mechanism for the following reaction that prepares flosal.how to synthesize 2-phenylclohexanone from cyclohexanone?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 step
- 2. Draw a plausible mechanism for the following transformation: [H₂SO4] excess EtOH -H₂O EtO OEtHow to synthesize the alkyl azide?1) 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.