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WE can convert the acetone in to t-butyl alcohol by the Grignard reagent.....
by grignard reaction.....
It is because t-butyl alcohol forms an intra-molecular hydrogen bonding i. e. while t-butyl alcohol does not.
Melting points:- water: 0 oC- tert-butyl alcohol: 25 oCBoiling points:- water: 100 oC- tert-butyl alcohol: 82 oC
Yes, they are miscible.
WE can convert the acetone in to t-butyl alcohol by the Grignard reagent.....
by grignard reaction.....
They are polar compounds.
Acetone
In I.U.P.A.C system terms Secondary and Tertiary are not used, but logically secondary should prior to tertiary.
It is because t-butyl alcohol forms an intra-molecular hydrogen bonding i. e. while t-butyl alcohol does not.
A butyl alcohol is any of four isomeric aliphatic alcohols derived from butane.
Butyl is not a compound but is part of a compound. Butyl simply means a 4 carbon chain, as in butyl alcohol, which is CH3CH2CH2CH2OH. This is a compound.
Tert-butyl alcohol is an intermediate in the production of MTBE and ETBE; also is used as a solvent.
Acetone 0.79; t-Butyl alcohol 0.79; Isopropyl alcohol 0.79; Methyl alcohol 0.79; Propionaldehyde 0.81
n-butyl alcohol and propionic anhydride are used.
you would get t-butyl chloride