ANACHEM 11 12 Flashcards

(67 cards)

1
Q

relationship between chemical reaction
and electricity (movement of electrons

A

ELECTROCHEMISTRY

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2
Q

it is the measurement of current/voltage
generated by the activity of an ion

A

ELECTROCHEMISTRY

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3
Q

Electrochemistry Analysis

A
  • redox titration
  • potentiometry - widely used
  • amperometry
  • polarography
  • electrogravimetry
  • voltammetry
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4
Q
  • A pair of
    electrodes in contact with an electrolyte
    solution
A

Electrochemical Cell

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5
Q

An
electrochemical cell which
spontaneously produces current (or
energy) when the electrodes are
connected externally by a
conducting wire.

A

. Galvanic or Voltaic Cell -

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6
Q

An electrochemical cell through
which current is forced by a battery
or some other external source of
energy. (such as battery, DC,
alternate current)

A

Electrolysis or Electrolytic Cell

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7
Q

The
algebraic sum of the individual electrode
potentials of an electrochemical cell at
zero current

A

Theoretical Cell Potential -

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8
Q
  • the amount of
    potential that is lost on the way from the
    reference electrode to the working
    electrodes.
A

Ohmic Drop, IR

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9
Q

A potential
developed across a boundary between
electrolytes differing in concentration or
chemical composition

A

Liquid-junction Potential

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10
Q

one way of measuring how
easily the substance loses on
electron.

A

Standard Electrode Potential

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11
Q

Electrode potential
measured in solutions where all
reactants and products are at
unit activity.

A

Standard Electrode Potential

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12
Q

The potential
of an electrode measured relative to a
standard, usually the SHE. It is a
measure of the driving force of the
electrode reaction and is temperature
and activity dependent

A

Electrode Potential E

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13
Q

This consists of a platinum electrode
coated with platinum black to catalyze
the electrode reaction and over the
surface of which hydrogen at 760 mm of
mercury is passed.

A

Standard Hydrogen Electrode

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14
Q

One in which the halfcell reactions are reversed by reversing
the current flow; such a cell is said to be
in thermodynamic equilibrium

A

REVERSIBLE CELL

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15
Q

The electrode at which
reduction occurs

A

CATHODE

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16
Q

The electrode at which
oxidation occurs.

A

ANODE

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17
Q

occur together but opposite
direction.

A

Half-cell Reactions

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17
Q

The additional
potential required to cause some
electrode reactions to proceed at an
appreciable rate

A

Activation Overpotential

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18
Q

Oxidation or reduction reaction
occurring at an electrode

A

Half-cell Reactions

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19
Q

In an oxidation/reduction reaction
electrons are transferred from one
reactant to another. (occurs together)

A

REDOX REACTIONS

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20
Q

consists of two conductors called
electrodes, each of which is
immersed in an electrolyte solution.

A

Electrochemical Cells

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20
Q
  • the
    additional voltage that is needed to carry
    out electrolysis in addition to the
    standard cell potential.
A

Concentration Overpotential

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21
Q

In most of the cells that will be of
interest to us, the solutions
surrounding the two electrodes are
different and must be separated to
avoid direct reaction between the
reactants

A

Electrochemical Cells

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22
Q

consume
electricity. In contrast to a voltaic cell,
requires an external source of
electrical energy for operation.

A

electrolytic cells

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22
store electrical energy.
Galvanic cells
23
: In redox methods an indicator electrode is used to sense the presence or change in concentration of the oxidized and reduced forms of a redox couple.
INDICATOR ELECTRODE
24
an electrode that has a stable and well known electrode potential.
REFERENCE ELECTRODE
25
The electrode consists of two concentric glass tubes, the inner one of which contains mercury in contact with a paste of mercury, mercury (1) chloride (calomel), and potassium chloride.
Calomel Electrode
26
This consists of a silver wire, coated with silver chloride and in contact with a solution of potassium chloride saturated with silver chloride
Silver-silver Chloride Electrode
26
Used to find the concentration of solute in a solution
Potentiometry
27
Potential is measured under the conditions of no current flow
Potentiometry
28
based on measuring the potential of electrochemical cells without drawing appreciable current.
Potentiometry
29
- w sample dilution;
INDIRECT ISE
29
an electrochemical transducer capable of responding to one given ion. they are selective and sensitive method; but not specific
ion-selective electrodes.
30
- w/o sample dilution;
DIRECT ISE
31
a potential that varies in the concentration of analyte
Indicator Electrode
32
Potentiometry USES
pH and pCO₂ tests
33
an accurately known electrode potential
Reference Electrode
34
ideal reference electrode has a potential that is accurately known. constant, and completely insensitive to the composition of the analyte solution
Reference Electrode
34
half-cell having a known electrode potential that remains constant at constant temperature and is independent of the composition of the analyte solutioN
Reference Electrode
35
Reference Electrode Some common examples
a. Saturated calomel electrode b. Silver/silver hydrogen electrode c. Standard hydrogen electrode d. pH electrode
35
has a potential that varies in a known way with variations in the concentration of an analyte.
INDICATOR ELECTRODE
35
ideal indicator electrode responds rapidly and reproducibly to changes in the concentration of an analyte ion
INDICATOR ELECTRODE
36
INDICATOR ELECTRODE TYPES
1. metallic, 2. membrane, and 3. ion-sensitive field effect transistors
37
One potential advantage of an ion-selective electrode is the ability to incorporate it into a flow cell for the continuous monitoring of wastewater streams.
➢ Environmental Chemistry
37
ion-selective electrodes are important sensors for clinical samples because of their selectivity for analytes in complex matrices
Clinical Chemistry.
38
Use a pH electrode to monitor the change in pH during the titration for determining the equivalence point of an acid-base titration.
Potentiometric Titrations.
39
the known pH of a reference solution is determined by using two electrodes, a glass electrode and a reference electrode, and measuring the voltage (difference in potential) generated between the two electrodes
glass-electrode method,
39
thin membrane is called the
Electrode membrane.
40
liquid inside the glass electrode usually has a pH o
7
40
immersed in a solution of unknown pH
glass electrode (indicator) and SCE (reference)
41
This other electrode, paired with the glass electrode, is called the
reference electrode
42
measurements provide a rapid and convenient method for determining the activity of a variety of cations and anions
Direct Potentiometry
42
e technique requires only a comparison of the potential developed in a cell containing the indicator electrode in the analyte solution with its potential when immersed in one or more standard solutions of known analyte concentration
Direct Potentiometry
43
serve as the internal reference for the glass electrode.
n indicator glass electrode and a silver/silver chloride reference —
44
measurements are also readily adapted to applications requiring req continuous and automatic recording of analytical data
Direct Potentiometry
44
endorsed by the National Institute of Standards and Technology (NIST), similar organizations is based upon potentiometric determination of pH of unknown solution followed after calibration of the meter with standard buffers
operational definition of pH
45
remarkably versatile tool for the measurement of pH under many conditions
glass/calomel electrode system
45
Values registered by the glass electrode tend to be somewhat high when the pH is less than about 0.5
The Acid Error
46
ordinary glass electrode tends to be somewhat sensitive to alkali metal ions and gives low readings at pH values greater than 9.
the Alkaline Error.( sodium error)
47
operational definition of pH is endorsed
National Institute of Standards and Technology (NIST) and the IUPAC
48
may cause erratic electrode performance.
Dehydration
49
has been found that significant errors may occur when the pH of samples of low ionic strength, such as lake or stream water, is measured with a glass/calomel electrode system
Errors in Low Ionic Strength Solutions.
50
A fundamental source of uncertainty for which a correction cannot be applied is the junction-potential variation resulting from differences in the composition of the standard and the unknown solution
Variation In Junction Potential
51
provide data that are more reliable than data from titrations that use chemical indicators and are particularly useful with colored or turbid solutions and for detecting the presence of unsuspected species.
Potentiometric Titrations
51
inaccuracies in the preparation of the buffer used for calibration or any changes in its composition during storage cause an error in subsequent pH measurements
Error in the pH Of The Standard Buffer
52
offer additional advantages over direct potentiometry. Because the measurement is based in the titrant volume that causes a rapid change in potential near the equivalence point,
Potentiometric titrations