An organic compound was synthesized and found to contain only c, h, n, o, and cl. it was observed that when a 0.150 g sample of
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The mass of ammonium chloride that must be added is : ( A ) 4.7 g
<u>Given data :</u>
Volume of water ( V ) = 250 mL = 0.25 L
pH of solution = 4.85
Kb = 1.8 * 10⁻⁵
Kw = 10⁻¹⁴
Given that the dissolution of NH₄Cl gives NH₄⁺⁺ and Cl⁻ ions the equation is written as :
NH₄CI + H₂O ⇄ NH₃ + H₃O⁺
where conc of H₃O⁺
[ H₃O⁺ ] = and Ka = Kw / Kb
∴ Ka = 5.56 * 10⁻¹⁰
Next step : Determine the concentration of H₃O⁺ in the solution
pH = - log [ H₃O⁺ ] = 4.85
∴ [ H₃O⁺ ] in the solution = 1.14125 * 10⁻⁵
Next step : Determine the concentration of NH₄CI in the solution
C = [ H₃O⁺ ]² / Ka
= ( 1.14125 * 10⁻⁵ )² / 5.56 * 10⁻¹⁰
= 0.359 mol / L
Determine the number of moles of NH₄CI in the solution
n = C . V
= 0.359 mol / L * 0.25 L = 0.08979 mole
Final step : determine the mass of ammonium chloride that must be added to 250 mL
mass = n * molar mass
= 0.08979 * 53.5 g/mol
= 4.80 g ≈ 4.7 grams
Therefore we can conclude that the mass of ammonium chloride that must be added is 4.7 g
Learn more about ammonium chloride : brainly.com/question/13050932
The strategy adopted for for the synthesis of <span>2-bromo-4-nitrobenzoic acid is as follow,
1) First Nitration of Toluene was done because the product formed (4-Nitrotoluene) will direct the next incoming electrophile (i.e. -Br) to ortho position with respect to -CH</span>₃ (ortho para directing) and at meta position with respect to -NO₂ (meta directing).
2) Bromination gave the exact desired product as discussed in point 1.
3) At last oxidation of toluene yield benzoic acid. No other substituent is oxidized other than -CH₃ group.
1) First Nitration of Toluene was done because the product formed (4-Nitrotoluene) will direct the next incoming electrophile (i.e. -Br) to ortho position with respect to -CH</span>₃ (ortho para directing) and at meta position with respect to -NO₂ (meta directing).
2) Bromination gave the exact desired product as discussed in point 1.
3) At last oxidation of toluene yield benzoic acid. No other substituent is oxidized other than -CH₃ group.