This organic chemistry video tutorial discusses the synthesis reaction mechanism of grignard reagents with water - H2O, D2O, aldehyes including formaldehyde, ketones, esters, acid chlorides, epoxides - ethylene oxide, CO2, etc. This video contains examples and practice problems that not only help you to predict the major product of the reaction but also how to choose the right reagents to synthesize a primary, secondary, and tertiary alcohol. In addition, other reactions were included in this video such as oxidation by H2CrO4, PCC, KMnO4 & H3O+, in addition to Na2Cr2O7 with H2SO4. Reduction of an alkyne to a cis alkene using H2 & lindlar's catalyst and to a trans alkene using Na and NH3 were also considered. The conversion of an alcohol into an alkyl halide using SOCl2 and PBr3 were also mentioned. The reagents used in this video include phenyl magnesium bromide, methyl magnesium bromide, ethyl magnesium bromide, acetyl chloride, cyclopentyl magnesium bromide, acetaldehyde, 2-butanone, etc.
Tagged under: grignard reagent,grignard reaction,mechanism,D2O,H2O,water,CO2,epoxide,acid chloride,ethylene oxide,ester,ketone,aldehydes,formaldehyde,primary alcohol,H2CrO4,secondary alcohol,tertiary alcohol,PCC,KMnO4,H3O+,lindlar' catalyst,Na NH3,phenylmagneisum bromide,methylmagnesium bromide,ethylmagnesium bromide,cyclopentylmagnesium bromide,grignard reagent reaction,grignard reagent synthesis
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