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Methyl amine, CH(3)NH(2) is a week base....

Methyl amine, `CH_(3)NH_(2)` is a week base. The expression for its ionization constant `K_(b)` is

A

`([CH_(3) NH_(3)^(+)][OH^(-)])/([CH_(3) NH_(2)][H_(2)O])`

B

`([CH_(2)NH_(3)^(+)][OH^(-)])/([CH_(3)NH_(2)])`

C

`([CH_(3) NH^(-)][H_(3)O^(+)])/([CH_(3)NH_(2)])`

D

`([CH_(3)NH_(2)])/([CH_(3)NH_(3)^(+)][OH^(-)])`

Text Solution

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The correct Answer is:
To derive the expression for the ionization constant \( K_b \) of methyl amine (\( CH_3NH_2 \)), follow these steps: ### Step 1: Write the ionization reaction When methyl amine is dissolved in water, it acts as a weak base and ionizes according to the following reaction: \[ CH_3NH_2 + H_2O \rightleftharpoons CH_3NH_3^+ + OH^- \] ### Step 2: Identify the products and reactants In this reaction: - The reactants are methyl amine (\( CH_3NH_2 \)) and water (\( H_2O \)). - The products are the methylammonium ion (\( CH_3NH_3^+ \)) and hydroxide ion (\( OH^- \)). ### Step 3: Write the expression for \( K_b \) The ionization constant \( K_b \) is defined as the ratio of the concentration of the products to the concentration of the reactants at equilibrium. Therefore, the expression for \( K_b \) can be written as: \[ K_b = \frac{[CH_3NH_3^+][OH^-]}{[CH_3NH_2]} \] ### Step 4: Consider the concentration of water Since water is the solvent and its concentration remains effectively constant, it is not included in the expression for \( K_b \). ### Final Expression Thus, the final expression for the ionization constant \( K_b \) of methyl amine is: \[ K_b = \frac{[CH_3NH_3^+][OH^-]}{[CH_3NH_2]} \]
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Amines are basic in nature due to the presence of lone pair of electrons on N atom of -NH_(2) group. The basic strength of amines can be expressed by their dissociation constant, K_(b) or pK_(b) . RNH_(2) + H_(2) to R NH_(3)^(+) + OH^(-) K_(b) = ([RHH_(3)^(+)][OH^(-)])/([RNH_(2)]) and pK_(b) = -log K_(b) Greater the K_(b) value or smaller the pK_(b) value, more is the basic strength of amine. Aliphatic amines are stronger bases than ammonia due to the electron releasing effect of alkyl groups. The basic strength among amines decreases as : 2^(@) gt 1^(@) gt 3^(@) Aryl amines such as aniline are less basic than aliphatic amines due to the involvement of lone pair of electrons on N atom with the resonance in benzene. In derivatives of aniline, the electron releasing groups increase the basic strength while electron withdrawing groups decrease the basic strength. The base weakening effect of electron withdrawing group and base strengthening effect of electron releasing group is more marked at p-position than at m-position. Every o- substituted aniline is less basic than aniline due to ortho effect. The strongest base among the following is

Amines are basic in nature due to the presence of lone pair of electrons on N atom of -NH_(2) group. The basic strength of amines can be expressed by their dissociation constant, K_(b) or pK_(b) . RNH_(2) + H_(2) to R NH_(3)^(+) + OH^(-) K_(b) = ([RHH_(3)^(+)][OH^(-)])/([RNH_(2)]) and pK_(b) = -log K_(b) Greater the K_(b) value or smaller the pK_(b) value, more is the basic strength of amine. Aliphatic amines are stronger bases than ammonia due to the electron releasing effect of alkyl groups. The basic strength among amines decreases as : 2^(@) gt 1^(@) gt 3^(@) Aryl amines such as aniline are less basic than aliphatic amines due to the involvement of lone pair of electrons on N atom with the resonance in benzene. In derivatives of aniline, the electron releasing groups increase the basic strength while electron withdrawing groups decrease the basic strength. The base weakening effect of electron withdrawing group and base strengthening effect of electron releasing group is more marked at p-position than at m-position. Every o- substituted aniline is less basic than aniline due to ortho effect. Which of the following statement is not correct?