An ecobotanist separates the components of a tropical bark extract by chromatography. She discovers a large proportion of quinidine, a dextrorotatory isomer of quinine used to control arrhythmic heartbeat. Quinidine has two basic nitrogens pKb1=5.4 and pKb2=10.To measure the concentration, she carries out a titration. Because of the low solubility of quinidine in water, she first protonates both nitrogens with excess HCl and titrates the acidified solution with standardized base. A 32.4 mg sample of quinidine is acidified with 7 mL of 0.15 M HCl.The volume of 0.1 M NaOH required to titrate the excess HCl isThe pH at the first equivalence point is
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Detailed Solution
nquinidine=32.4×10−3324=10−4nHCl added=7×10−3×0.15=10.5×10−4nHCl reqd. to neutralize quinidine=2×10−4 (as it is diacidic base)nHCl unreacted=10.5×10−4−2×10−4 = 8.5×10−4nNaOH for unreacted HCl=8.5×10−4=0.1×V×10−3⇒V=8.5 mLLet QH22+ is the fully protonated form of quinidine.QH22+⇌pKa1=14−10=4QH +⇌pKa2=14−5.4=8.6QAt first equivalence point there will only be QH+.⇒pH=pKa1+pKa22=6.3