ORGANIC CHEMISTRY 1 TERM ACCESS
ORGANIC CHEMISTRY 1 TERM ACCESS
3rd Edition
ISBN: 9781119661511
Author: Klein
Publisher: WILEY
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Chapter 17.5, Problem 15ATS
Interpretation Introduction

Interpretation For the given compounds, it should be determined which compound is expected to have lower pKa value

Concept introduction:

  • Ka is the acid dissociation constant of a solution
  • pKa=-log10[Ka]
  • For the stronger acids pKa value will be lower and  more stable
  • For the weaker acids pKa value will be higher and less stable
  • For stronger acids, its conjugate base is more stable
  • For weaker acids, its conjugate base is less stable.
  • Conjugate base is formed by the deprotonation of the parent acid
  • Aromatic compounds are more stable than non-aromatic compound
  • In order for the heterocycle to achieve a continuous system of overlapping p orbitals, the lone pair of the hetero atom must occupy a p orbital with six π electrons that is four from the π bonds and two from the lone pair. Then this compound is aromatic.

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Use the average molarity of acetic acid (0.0867M) to calculate the concentration in % (m/v). Then calculate the % difference between the calculated concentrations of your unknown vinegar solution with the 5.00% (w/v%) vinegar solution (check the formula for % difference in the previous lab or online). Before calculating the difference with vinegar, remember that this %(m/v) is of the diluted solution. It has been diluted 10 times.
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ORGANIC CHEMISTRY 1 TERM ACCESS

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