Chapter 2: 44P (page 140)
Compare the relative acidity of 1-molar aqueous solutions of the following acids.
Chapter 2: 44P (page 140)
Compare the relative acidity of 1-molar aqueous solutions of the following acids.
All the tools & learning materials you need for study success - in one app.
Get started for freeClassify the following hydrocarbons, and draw a lewis structure for each one. A compound may fit into more than one of the following classifications:
Alkane, alkene, alkyne, cycloalkane, cycloalkene, cycloalkyne, aromatic hydrocarbon.
e.
f.
g.
h.
i.
Draw a Lewis structure, and classify each of the following compounds. The possible classification are as follows:
alcohol, ketone, carboxylic acid, ether, aldehyde and alkene.
(a)
(b)
(c)
(d)
(e)
(f)
(g)
(h)
(i)
Which of the following pure compounds can form hydrogen bonds? Which can form hydrogen bonds with water? Which ones do you expect to be soluble in water?
(a)
(b)
(c)
(d)
(e)
(f)
(g)
(h)
(i)
(j)
(k)
(l)
The pKa of ascorbic acid (vitamin C, page 9) is 4.17 , showing that it is lightly more acidic than acetic acid (CH3COOH,pKa =4.74) .
(a)Show four different conjugate bases that would be formed by deprotonation of the four different OH groups in ascorbic acid.
(b) Compare the stabilities of these four conjugate bases, and predict which OH group of ascorbic acid is the most acidic.
(c) Compare the most stable conjugate base of ascorbic acid with the conjugate base of acetic acid, and suggest why these two compounds have similar acidities, even though ascorbic acid lacks the carboxylic acid (COOH ) group
Write equations for the following acid- base reactions. Use the information in Table 2.2 or Appendix 4 to predict whether the equilibrium will favor the reactants or the products.
(a)
(b)
(c)
(d)
(e)
(f)
(g)
(h)
(i)
(j)
What do you think about this solution?
We value your feedback to improve our textbook solutions.