The basic strength of alkylamines in the aqueous phase is not decided by . . . . . . .

  • A
    Inductive effect
  • B
    Solvation effect
  • C
    Steric hindrance
  • D
    Hyperconjugation effect

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Similar Questions

The action of nitrous acid with ethylamine produces:

What is obtained by the ammonolysis of alkyl halides?

Which statement is not correct?

Aniline dissolved in dilute $HCl$ is reacted with sodium nitrite at $0\,^oC$. This solution was added dropwise to a solution containing an equimolar mixture of aniline and phenol in dilute $HCl$. The structure of the major product is

Rank the following species in order of decreasing nucleophilicity in a polar protic solvent (most $\to$ least nucleophilic):
$(1) \ CH_3CH_2CH_2O^{-}$,$(2) \ CH_3CH_2CH_2S^{-}$,$(3) \ CH_3CH_2C(=O)O^{-}$

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