The reaction sequence is as follows:
Step 1: Reaction of ethanamine with \(\text{NaNO}_2\) and \(\text{HCl}\)
Ethanamine (\(\text{CH}_3\text{CH}_2\text{NH}_2\)) reacts with \(\text{NaNO}_2\) and \(\text{HCl}\) to form an unstable diazonium salt (\(\text{CH}_3\text{CH}_2\text{N}_2^+\text{Cl}^-\)):
\[\text{CH}_3\text{CH}_2\text{NH}_2 + \text{NaNO}_2 + \text{HCl} \rightarrow \text{CH}_3\text{CH}_2\text{N}_2^+\text{Cl}^- + \text{NaCl} + \text{H}_2\text{O}.\]
Step 2: Hydrolysis of the diazonium salt
The diazonium salt decomposes upon hydrolysis, liberating \(\text{N}_2\), \(\text{HCl}\), and ethanol (\(\text{CH}_3\text{CH}_2\text{OH}\)):
\[\text{CH}_3\text{CH}_2\text{N}_2^+\text{Cl}^- + \text{H}_2\text{O} \rightarrow \text{CH}_3\text{CH}_2\text{OH} + \text{N}_2 + \text{HCl}.\]
Step 3: Calculation of the mass of ethanamine
The reaction generates \(0.2\) moles of \(\text{HCl}\), which neutralizes \(0.2\) moles of \(\text{NaOH}\). From the stoichiometry of the reaction, 1 mole of ethanamine produces 1 mole of \(\text{HCl}\). Therefore, the moles of ethanamine (\(\text{CH}_3\text{CH}_2\text{NH}_2\)) required are \(0.2\) moles.
The molar mass of ethanamine is:
\[\text{Molar mass of } \text{CH}_3\text{CH}_2\text{NH}_2 = 12 + 3 + 3 + 12 + 2 + 14 + 1 = 44 \, \text{g/mol}.\]
The mass of ethanamine is:
\[\text{Mass} = \text{Moles} \times \text{Molar mass} = 0.2 \times 44 = 8.8 \, \text{g} \, (\text{Nearest Integer to } 9).\]
Final Answer: \(X = 9\).
Amines are usually formed from amides, imides, halides, nitro compounds, etc. They exhibit hydrogen bonding which influences their physical properties. In alkyl amines, a combination of electron releasing, steric and H-bonding factors influence the stability of the substituted ammonium cations in protic polar solvents and thus affect the basic nature of amines. Alkyl amines are found to be stronger bases than ammonia. Amines being basic in nature, react with acids to form salts. Aryldiazonium salts, undergo replacement of the diazonium group with a variety of nucleophiles to produce aryl halides, cyanides, phenols and arenes.
Amines are usually formed from amides, imides, halides, nitro compounds, etc. They exhibit hydrogen bonding which influences their physical properties. In alkyl amines, a combination of electron releasing, steric and H-bonding factors influence the stability of the substituted ammonium cations in protic polar solvents and thus affect the basic nature of amines. Alkyl amines are found to be stronger bases than ammonia. Amines being basic in nature, react with acids to form salts. Aryldiazonium salts, undergo replacement of the diazonium group with a variety of nucleophiles to produce aryl halides, cyanides, phenols and arenes.
Arrange the following in increasing order of their basic strength in aqueous solution:
CH$_3$–NH$_2$, (CH$_3$)$_2$NH, (CH$_3$)$_3$N
Amines are usually formed from amides, imides, halides, nitro compounds, etc. They exhibit hydrogen bonding which influences their physical properties. In alkyl amines, a combination of electron releasing, steric and H-bonding factors influence the stability of the substituted ammonium cations in protic polar solvents and thus affect the basic nature of amines. Alkyl amines are found to be stronger bases than ammonia. Amines being basic in nature, react with acids to form salts. Aryldiazonium salts, undergo replacement of the diazonium group with a variety of nucleophiles to produce aryl halides, cyanides, phenols and arenes.