問題一覧
1
5.19×10-7 m/s
2
To ensure clear visibility of the boundary
3
0.71
4
The solvent's intermolecular forces
5
increases with an increase in temperature due to decreased viscosity and higher thermal energy.
6
the sum of the individual ionic conductivities of cations and anions.
7
the development of an ionic atmosphere that opposes the applied electric field.
8
The magnitude of the applied external electric field
9
The magnitude of the electric field
10
2.5×10-2 m/s
11
The relative mobilities of cations and anions
12
Halves
13
5×10-2
14
35ms cm2/mol
15
0.2mol/L
16
0.103
17
Dilution reduces the number of ions per unit volume but increases the mobility of ions, enhancing molar conductance.
18
K decreases, while Am increases because of higher degree of ionization.
19
0.01S cm-1
20
Manufacturing of high-purity water in the pharmaceutical industry
21
a=0.103, weak electrolyte
22
It increases linearly
23
300S cm2 mol-1
24
6.67
25
AC minimizes the polarization effect at the electrodes, providing accurate conductance measurements.
26
0.01M
27
Compare the molar conductance (Am) at infinite dilution with the limiting molar conductance (Am) for a similar strong electrolyte.
28
Strong acid vs. strong base
29
1.00mS/cm
30
67.00ppm
31
Sparingly soluble salts partially dissociate, and the concentration of ions in solution can be deduced from the conductance.
32
The degree of dissociation of a weak electrolyte increases with dilution, enhancing molar conductivity.
33
Conductance provides the combined concentration of H+ and OH- ions, which can be used to calculate Kw.
34
0.01M
35
1.04mS/cm
36
High conductivity typically indicates the presence of dissolved salts, which may lower water quality.
37
1.25×10-4 mol/L
38
Decrease in ionic mobility due to interionic interactions
39
1.0×10-14 mol2/1.2
40
Conductance directly correlates to the concentration of all ions present in a solution, providing insights into electrolyte balance.
41
1.8×10-4 mol/L
42
The relative reduction potentials of the electrodes.
43
1.56V
44
1.8×10-5 mol/L
45
A concentration cell generates EMF based on a concentration difference, while a galvanic cell relies on electrode potential differences.
46
0.43V
47
It accounts for the effect of concentration and temperature on cell potential.
48
EMF increases as the conductance of the electrolyte increases, due to more efficient ion movement.
49
The EMF of a battery reflects its ability to do work, but efficiency is determined by the internal resistance.
50
Measuring the electromotive force (EMF) of a saturated solution in a galvanic cell
51
An increase in the conductance of the electrolyte solution generally decreases the EMF, since less voltage is needed for ion migration.
52
Decreasing the concentration of lithium ions at the cathode.
53
The relative position of the metal in the EMF series
54
-214.8kJ/mol
55
It allows the calculation of Ksp without needing to know the concentration of the ions directly.
56
-211kJ/mol
57
A platinum electrode in contact with hydrogen gas and a solution of H+ ions
58
In a galvanic cell, the cathode is positive, while in an electrolytic cell, the cathode is negative.
59
It selectively responds to the activity of a specific ion in solution by generating a potential difference.
60
It facilitates a reversible redox reaction involving the transfer of electrons between the electrode and solution.
61
-31.0kJ/mol
62
Oxidation of metal to metal ions
63
4.78×1010
64
Platinum electrode in contact with chlorine gas and chloride ions
65
It maintains electrical neutrality by allowing the migration of ions.
66
It facilitates the generation of a potential difference by selectively binding to fluoride ions.
67
The electrode allows the oxidation of Fe2+ to Fe3+ and the reduction of Fe3+ to Fe2+.
68
The glass electrode develops a potential difference across its membrane, which depends on the activity of H+ ions in solution.
69
The exchange of hydrogen ions with alkali metal ions in the hydrated layer of the glass membrane.
70
It must maintain a constant and stable potential under varying solution conditions.
71
They integrate the reference and sensing electrodes into a single probe to minimize junction potential errors.
72
It is expressed as x/m=kP1/n (where n>1)
73
To provide a stable and known potential against which the glass electrode's potential can be measured.
74
It provides a constant internal reference potential for the measurement.
75
To maintain electrical contact with the solution while minimizing contamination of the reference solution
76
They eliminate the need for regular refilling of the reference electrolyte.
77
Adsorption is reversible and involves monolayer coverage of the surface.
78
BET isotherm.
79
Type 1
80
Weak adsorbate-adsorbent interactions.
81
Henry's law isotherm
82
Type IV
83
The rate-determining step
84
200 seconds
85
0.250mol/L
86
25s
87
Multilayer adsorption followed by capillary condensation in mesopores.
88
Type II
89
Capillary condensation within the pores.
90
Adsorption reaches a maximum (plateau) due to monolayer formation.
91
Increases linearly with P.
92
Pathway 1 (Ea(1)-40kJ/mol)
93
346 seconds
94
100s
95
25s
96
The rate of the reaction is proportional to the cube of the concentration of a single reactant.
97
5×106 s-1
98
It facilitates mass transport by inducing controlled convection near the electrode surface.
99
It reduces solution resistance effects due to its small size.
biochem
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21問 • 9ヶ月前問題一覧
1
5.19×10-7 m/s
2
To ensure clear visibility of the boundary
3
0.71
4
The solvent's intermolecular forces
5
increases with an increase in temperature due to decreased viscosity and higher thermal energy.
6
the sum of the individual ionic conductivities of cations and anions.
7
the development of an ionic atmosphere that opposes the applied electric field.
8
The magnitude of the applied external electric field
9
The magnitude of the electric field
10
2.5×10-2 m/s
11
The relative mobilities of cations and anions
12
Halves
13
5×10-2
14
35ms cm2/mol
15
0.2mol/L
16
0.103
17
Dilution reduces the number of ions per unit volume but increases the mobility of ions, enhancing molar conductance.
18
K decreases, while Am increases because of higher degree of ionization.
19
0.01S cm-1
20
Manufacturing of high-purity water in the pharmaceutical industry
21
a=0.103, weak electrolyte
22
It increases linearly
23
300S cm2 mol-1
24
6.67
25
AC minimizes the polarization effect at the electrodes, providing accurate conductance measurements.
26
0.01M
27
Compare the molar conductance (Am) at infinite dilution with the limiting molar conductance (Am) for a similar strong electrolyte.
28
Strong acid vs. strong base
29
1.00mS/cm
30
67.00ppm
31
Sparingly soluble salts partially dissociate, and the concentration of ions in solution can be deduced from the conductance.
32
The degree of dissociation of a weak electrolyte increases with dilution, enhancing molar conductivity.
33
Conductance provides the combined concentration of H+ and OH- ions, which can be used to calculate Kw.
34
0.01M
35
1.04mS/cm
36
High conductivity typically indicates the presence of dissolved salts, which may lower water quality.
37
1.25×10-4 mol/L
38
Decrease in ionic mobility due to interionic interactions
39
1.0×10-14 mol2/1.2
40
Conductance directly correlates to the concentration of all ions present in a solution, providing insights into electrolyte balance.
41
1.8×10-4 mol/L
42
The relative reduction potentials of the electrodes.
43
1.56V
44
1.8×10-5 mol/L
45
A concentration cell generates EMF based on a concentration difference, while a galvanic cell relies on electrode potential differences.
46
0.43V
47
It accounts for the effect of concentration and temperature on cell potential.
48
EMF increases as the conductance of the electrolyte increases, due to more efficient ion movement.
49
The EMF of a battery reflects its ability to do work, but efficiency is determined by the internal resistance.
50
Measuring the electromotive force (EMF) of a saturated solution in a galvanic cell
51
An increase in the conductance of the electrolyte solution generally decreases the EMF, since less voltage is needed for ion migration.
52
Decreasing the concentration of lithium ions at the cathode.
53
The relative position of the metal in the EMF series
54
-214.8kJ/mol
55
It allows the calculation of Ksp without needing to know the concentration of the ions directly.
56
-211kJ/mol
57
A platinum electrode in contact with hydrogen gas and a solution of H+ ions
58
In a galvanic cell, the cathode is positive, while in an electrolytic cell, the cathode is negative.
59
It selectively responds to the activity of a specific ion in solution by generating a potential difference.
60
It facilitates a reversible redox reaction involving the transfer of electrons between the electrode and solution.
61
-31.0kJ/mol
62
Oxidation of metal to metal ions
63
4.78×1010
64
Platinum electrode in contact with chlorine gas and chloride ions
65
It maintains electrical neutrality by allowing the migration of ions.
66
It facilitates the generation of a potential difference by selectively binding to fluoride ions.
67
The electrode allows the oxidation of Fe2+ to Fe3+ and the reduction of Fe3+ to Fe2+.
68
The glass electrode develops a potential difference across its membrane, which depends on the activity of H+ ions in solution.
69
The exchange of hydrogen ions with alkali metal ions in the hydrated layer of the glass membrane.
70
It must maintain a constant and stable potential under varying solution conditions.
71
They integrate the reference and sensing electrodes into a single probe to minimize junction potential errors.
72
It is expressed as x/m=kP1/n (where n>1)
73
To provide a stable and known potential against which the glass electrode's potential can be measured.
74
It provides a constant internal reference potential for the measurement.
75
To maintain electrical contact with the solution while minimizing contamination of the reference solution
76
They eliminate the need for regular refilling of the reference electrolyte.
77
Adsorption is reversible and involves monolayer coverage of the surface.
78
BET isotherm.
79
Type 1
80
Weak adsorbate-adsorbent interactions.
81
Henry's law isotherm
82
Type IV
83
The rate-determining step
84
200 seconds
85
0.250mol/L
86
25s
87
Multilayer adsorption followed by capillary condensation in mesopores.
88
Type II
89
Capillary condensation within the pores.
90
Adsorption reaches a maximum (plateau) due to monolayer formation.
91
Increases linearly with P.
92
Pathway 1 (Ea(1)-40kJ/mol)
93
346 seconds
94
100s
95
25s
96
The rate of the reaction is proportional to the cube of the concentration of a single reactant.
97
5×106 s-1
98
It facilitates mass transport by inducing controlled convection near the electrode surface.
99
It reduces solution resistance effects due to its small size.