1.

The correct order of increasing basicity of the given conjugate bases (R=CH_(3)) is

Answer»

`CRCOO^(-) lt NH_(2)^(-) lt HC -= C^(-) lt R^(-)`
`RCO O^(-) lt HC -= C^(-) lt NH_(2)^(-) lt R^(-)`
`RCO O^(-) lt HC -= C^(-) lt R^(-) lt NH_(2)^(-)`
`R^(-) lt HC -= C^(-) lt RCO O^(-) lt NH_(2)^(-)`

Solution :The conjugate acids of the given bases are `RCOOHgtCH-=CHgtNH_(3)gtRH`. Their acidic strengths are in the order : `RCOOHgtCH-=CHgtNH_(3)gtRH`.As STRONG acid has weak conjugate BASE, the BASIC strenths of the given bases will be in the order :
`RCOO^(-)ltHC-=C^(-)ltNH_(2)^(-)LTR^(-)` (Remember that `sp^(3)` C is less electronegative than `sp^(3)` N. Hence, alkyl carbanion `(R^(-))` is more basic than `bar(N)H_(2)`. However, sp-hybridized carbon is more electronegative than `sp^(3)` N Hence `bar(N)H_(2)` is more basic `HC-=bar(C)`.


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