OWLV2 FOR MASTERTON/HURLEY'S CHEMISTRY:
8th Edition
ISBN: 9781305079304
Author: Hurley
Publisher: IACCENGAGE
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Textbook Question
Chapter 3, Problem 29QAP
The active ingredient in Pepto-Bismo® (an over- the-counter remedy for an upset stomach) is bismuth sub-salicylate, C7H5BiO4. Analysis of a 1.7500-g sample of Pepto-Bismol yields 346 mg of bismuth. What percent by mass is bismuth subsalicylate in the sample? (Assume that there are no other bismuth-containing compounds in Pepto-Bismol.)
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Q6: Using acetic acid as the acid, write the balanced chemical equation for the protonation of
the two bases shown (on the -NH2). Include curved arrows to show the mechanism.
O₂N-
O₂N.
-NH2
-NH2
a) Which of the two Bronsted bases above is the stronger base? Why?
b) Identify the conjugate acids and conjugate bases for the reactants.
c) Identify the Lewis acids and bases in the reactions.
Q5: For the two reactions below:
a) Use curved electron-pushing arrows to show the mechanism for the reaction in the
forward direction. Redraw the compounds to explicitly illustrate all bonds that are broken
and all bonds that are formed.
b) Label Bronsted acids and bases in the left side of the reactions.
c) For reaction A, which anionic species is the weakest base? Which neutral compound is
the stronger acid? Is the forward or reverse reaction favored?
d) Label Lewis acids and bases, nucleophiles and electrophiles in the left side of the
reactions.
A.
용
CH3OH
я хон
CH3O
OH
B. HBr
CH3ONa
NaBr
CH3OH
potential energy
Br
b) Translate the Newman projection below to its wedge-and-dash drawing.
F
H.
OH
CH3
CI
c) Isopentane (2-methylbutane) is a compound containing a branched carbon chain. Draw
a Newman projection of six conformations about the C2-C3 bond of isopentane. On the
curve of potential energy versus angle of internal rotation for isopentane, label each
energy maximum and minimum with one of the conformations.
0°
。
F
A
B
D
C
angle of internal rotation
E
F
360° (=0°)
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Chapter 3 Solutions
OWLV2 FOR MASTERTON/HURLEY'S CHEMISTRY:
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