Salicylic acid, HOC 6 H 4 CO 2 H, and its derivatives have been used as pain relievers for a long time. Salicylic acid occurs in small amounts in the leaves, bark, and roots of some vegetation (most notably historically in the bark of the willow tree). Extracts of these plants have been used as medications for centuries. The acid was first isolated in the laboratory in 1838. (a) Bath functional groups of salicylic acid ionize in water, with K a = 1.0 × 10 − 3 for the—CO 2 H group and 4.20 × 10 − 13 for the -OH group. What is the pH of a saturated solution of the acid (solubility = 1.8 g/L).. (b) Aspirin was discovered as a result of efforts to produce a derivative of salicylic acid that would not be irritating to the stomach lining. Aspirin is acetylsalicylic acid, CH 3 CO 2 C 6 H 4 CO 2 H. The -CO 2 H functional group is still present, but its acidity is reduced, K a = 3.0 × 10 − 4 . What is the pH of a solution of aspirin with the same concentration as a saturated solution of salicylic acid (See Part a). (c) Under some conditions, aspirin reacts with water and forms a solution of salicylic acid and acetic acid: CH 3 CO 2 C 6 H 4 CO 2 H ( a q ) + H 2 O ( l ) → HOC 6 H 4 CO 2 H ( a q ) + CH 3 CO 2 H ( a q ) i. Which of the acids, salicylic acid or acetic acid, produces more hydronium ions in such a solution? ii. What are the concentrations of molecules and ions in a solution produced by the hydrolysis of 0.50 g of aspirin dissolved in enough water to give 75 mL of solution?
Salicylic acid, HOC 6 H 4 CO 2 H, and its derivatives have been used as pain relievers for a long time. Salicylic acid occurs in small amounts in the leaves, bark, and roots of some vegetation (most notably historically in the bark of the willow tree). Extracts of these plants have been used as medications for centuries. The acid was first isolated in the laboratory in 1838. (a) Bath functional groups of salicylic acid ionize in water, with K a = 1.0 × 10 − 3 for the—CO 2 H group and 4.20 × 10 − 13 for the -OH group. What is the pH of a saturated solution of the acid (solubility = 1.8 g/L).. (b) Aspirin was discovered as a result of efforts to produce a derivative of salicylic acid that would not be irritating to the stomach lining. Aspirin is acetylsalicylic acid, CH 3 CO 2 C 6 H 4 CO 2 H. The -CO 2 H functional group is still present, but its acidity is reduced, K a = 3.0 × 10 − 4 . What is the pH of a solution of aspirin with the same concentration as a saturated solution of salicylic acid (See Part a). (c) Under some conditions, aspirin reacts with water and forms a solution of salicylic acid and acetic acid: CH 3 CO 2 C 6 H 4 CO 2 H ( a q ) + H 2 O ( l ) → HOC 6 H 4 CO 2 H ( a q ) + CH 3 CO 2 H ( a q ) i. Which of the acids, salicylic acid or acetic acid, produces more hydronium ions in such a solution? ii. What are the concentrations of molecules and ions in a solution produced by the hydrolysis of 0.50 g of aspirin dissolved in enough water to give 75 mL of solution?
Salicylic acid, HOC6H4CO2H, and its derivatives have been used as pain relievers for a long time. Salicylic acid occurs in small amounts in the leaves, bark, and roots of some vegetation (most notably historically in the bark of the willow tree). Extracts of these plants have been used as medications for centuries. The acid was first isolated in the laboratory in 1838.
(a) Bath functional groups of salicylic acid ionize in water, with
K
a
=
1.0
×
10
−
3
for the—CO2H group and
4.20
×
10
−
13
for the -OH group. What is the pH of a saturated solution of the acid (solubility = 1.8 g/L)..
(b) Aspirin was discovered as a result of efforts to produce a derivative of salicylic acid that would not be irritating to the stomach lining. Aspirin is acetylsalicylic acid, CH3CO2C6H4CO2H. The -CO2H functional group is still present, but its acidity is reduced,
K
a
=
3.0
×
10
−
4
. What is the pH of a solution of aspirin with the same concentration as a saturated solution of salicylic acid (See Part a).
(c) Under some conditions, aspirin reacts with water and forms a solution of salicylic acid and acetic acid:
CH
3
CO
2
C
6
H
4
CO
2
H
(
a
q
)
+
H
2
O
(
l
)
→
HOC
6
H
4
CO
2
H
(
a
q
)
+
CH
3
CO
2
H
(
a
q
)
i. Which of the acids, salicylic acid or acetic acid, produces more hydronium ions in such a solution?
ii. What are the concentrations of molecules and ions in a solution produced by the hydrolysis of 0.50 g of aspirin dissolved in enough water to give 75 mL of solution?
Definition Definition Group of atoms that shape the chemical characteristics of a molecule. The behavior of a functional group is uniform in undergoing comparable chemical reactions, regardless of the other constituents of the molecule. Functional groups aid in the classification and anticipation of reactivity of organic molecules.
6. Match each of the lettered items in the column on
the left with the most appropriate numbered
item(s) in the column on the right. Some of the
numbered items may be used more than once
and some not at all.
a.
Z = 37
1.
b.
Mn
2.
C.
Pr
element in period 5 and group
14
element in period 5 and group
15
d. S
e. [Rn] 7s¹
f.
d block
metal
3. highest metallic character of all
the elements
4. paramagnetic with 5 unpaired
electrons
5. 4f36s2
6. isoelectronic with Ca²+ cation
7.
an alkaline metal
8. an f-block element
Draw all formal charges on the structures below as is and draw 1 resonance structure that is more stable.
Part II. xiao isolated a compound TAD (Ca H 10 N₂) from tobacco and obtained its IR spectrum. Xiao proposed
a chemical structure shown below:
% Transmittance
4000
3500
3000
2500 2000
Wavenumber (cm-1)
1500
1000
(a) Explain why her proposed structure is inconsistent with the IR spectrum obtained
(b) TAD exists as a tautomer of the structure xiao proposed. Draw the structure
and explain why it is more compatible with the obtained spectrum.
(C) what is the possible source for the fairly intense signal at
1621cm1
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