Explanation of the separation of triphenymethanol in the Grignard experiment?
i am assuming your grignard reaction finished
after gignard reaction finished add the dilute HCl to the reaction mixture to hydrlyse the O-Mgbr bond
reaction solvent is ether after addition of dilute HCl you will clearly see two layers
top layer is ether layer, bottom layer is aq layer (means dil HCl)
triphenyl methanol is in ether layer
remaining things are in water layer
separate both layers using separating funnel
then extract the water layer using fresh ether two times
combine all the ether layers and then wash with water once
the resultent ether was dried over anhydrous sodium sulphate
then concetrate in rotery evaparater you will get the final product
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