Problems for Chapter 8 8

PROBLEM 1
How would you separate a mixture of these three compounds?

PROBLEM 2
In the separation of benzoic acid from toluene on p. 164 of the textbook we
suggested using KOH solution. How concentrated a solution would be
necessary to ensure that the pH was above the pKa of benzoic acid (4.2)? How
would you estimate how much KOH solution to use?

PROBLEM 3
What species would be present in a solution of this hydroxy-acid in (a) water at
pH 7, (b) aqueous alkali at pH 12, and (c) in concentrated mineral acid?

PROBLEM 4
What would you expect to be the site of (a) protonation and (b) deprotonation
if these compounds were treated with the appropriate acid or base? In each
case suggest a suitable acid or base and give the structure of the products.
24 Problems to accompany Organic Chemistry

PROBLEM 5
Suggest what species would be formed by each of these combinations of
reagents. You are advised to use estimated pKa values to help you and to beware
of those cases where nothing happens.

PROBLEM 6
What is the relationship between these two molecules? Discuss the structure of
the anion that would be formed by the deprotonation of each compound.

PROBLEM 7
The carbon NMR spectrum of these compounds can be run in D 2O under the
conditions shown. Why are these conditions necessary? What spectrum would
you expect to observe?
 Problems for Chapter 8 Acidity, basicity and pKa 25

PROBLEM 8
These phenols have approximate pKa values of 4, 7, 9, 10, and 11. Suggest with
explanations which pKa value belongs to which phenol.

PROBLEM 9
The pKa values of these two amino acids are as follows:
(a) cysteine: 1.8, 8.3, and 10.8
(b) arginine: 2.2, 9.0, and 13.2.
Assign these pKa values to the functional groups in each amino acid and draw
the most abundant structure that each molecule will have at pH 1, 7, 10, and
14.

PROBLEM 10
Neither of these two methods for making pentan-1,4-diol will work. What will
happen instead?
26 Problems to accompany Organic Chemistry

PROBLEM 11
Which of these bases would you choose to deprotonate the following
molecules? Very strong bases are more challenging to handle so you should
aim to use a base which is just strong enough for the job, but not unnecessarily
strong.