The correct order of basic strengths of the g | vedclass

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(D) The basic strength of amines depends on the inductive effect,solvation effect,and steric hindrance. $(a)$ For methyl-substituted amines in a polar

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(D) The basic strength of amines depends on the inductive effect,solvation effect,and steric hindrance. $(a)$ For methyl-substituted amines in a polar protic solvent,the order is $Me_2NH > MeNH_2 > Me_3N > NH_3$. $(b)$ For ethyl-substituted amines in a polar protic solvent,the order is $Et_2NH > Et_3N > EtNH_2 > NH_3$. $(c)$ In the gas phase,the solvation effect is absent,and the basicity is determined by the inductive effect of alkyl groups,leading to the order $3^o > 2^o > 1^o > NH_3$ (i.e.,$Me_3N > Me_2NH > MeNH_2 > NH_3$). Since all these statements are correct,the correct option is $D$.

The correct order of basic strengths of the given amines is:

Similar Questions

Consider the following sequence of reactions to produce major product $(A)$. Molar mass of product $(A)$ is $........... \ g \ mol^{-1}$. (Given molar mass in $g \ mol^{-1}$ of $C : 12, H : 1, O : 16, Br : 80, N : 14, P : 31$)

Benzyl isocyanide can be obtained from which of the following reactions? Choose the correct answer from the options given below:
$A$. Benzyl bromide + $AgCN$
$B$. Benzylamine + $CHCl_3$ + $Aq. NaOH$
$C$. Bromobenzene + $AgCN$
$D$. Aniline + $CHCl_3$ + $Aq. NaOH$
$E$. $2-$Phenylethyl bromide + $KCN$

Identify $A$ and $B$ in the following reaction sequence:
Aniline $\xrightarrow[KCN]{NaNO_2/HCl} (A)$ $\xrightarrow{SnCl_2/HCl/H_3O^+} (B)$

The product $(A)$ of the given reaction is:

Give a plausible explanation for each of the following:
$(i)$ Why are amines less acidic than alcohols of comparable molecular masses?
$(ii)$ Why do primary amines have higher boiling points than tertiary amines?
$(iii)$ Why are aliphatic amines stronger bases than aromatic amines?

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