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5 October, 14:54

In comparison to piperazine, the inductive effect will cause the pkb of methyl-piperazine to be:

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  1. 5 October, 16:43
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    In comparison to piperazine, the inductive effect will cause the pKb of methyl-piperazine to be "lower because the electron donating methyl group will make it a stronger base".

    methyl-group: electron-giving

    the inductive impact with electron-giving make the base more stronger - > lower pKa

    The pKb is a proportion of basicity, where a littler pKb value compares to a stronger base.

    This electron-giving expands the accessibility of electron charge thickness accessible to give, consequently increasing the quality or strength of N-methyl piperazine to go about as a Lewis base.
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