CONTENTS
INTRODUCTION
CONCEPTS OF WALSH DIAGRAM
APPLICATION IN TRIATOMIC MOLECULES
[IN AH₂ TYPE OF MOLECULES(BeH₂,BH₂,H₂O)]
INTRODUCTION
Arthur Donald Walsh FRS The introducer of walsh diagram (8 August 1916-23 April 1977) was a British chemist, professor of chemistry at the University of Dundee . He was elected FRS in 1964. He was educated at Loughborough Grammar School.
Walsh diagrams were first introduced in a series of ten papers in one issue of the Journal of the Chemical Society . Here, he aimed to rationalize the shapes adopted by polyatomic molecules in the ground state as well as in excited states, by applying theoretical contributions made by Mulliken .
Electrochemistry,Electrolytic and Metallic Conduction,Specific Resistance or resistivity (ρ),Specific Conductance or Conductivity (κ),Equivalent Conductance (Λ), Molar Conductance (Λm),Variation of Conductance with Dilution,Debye-Hückel-Onsager Equation,Kohlransch’s Law of Independent Migration of Ions,Faraday’s Laws of Electrolysis,Electrochemical Cells,The Nernst Equation,Oxidation Number
Oxidation Number / State Method For Balancing Redox Reactions,Half-Reaction or Ion-Electron Method For Balancing Redox Reactions,Half-Reaction or Ion-Electron Method For Balancing Redox Reactions,Common Oxidising and Reducing Agents
CONTENTS
INTRODUCTION
CONCEPTS OF WALSH DIAGRAM
APPLICATION IN TRIATOMIC MOLECULES
[IN AH₂ TYPE OF MOLECULES(BeH₂,BH₂,H₂O)]
INTRODUCTION
Arthur Donald Walsh FRS The introducer of walsh diagram (8 August 1916-23 April 1977) was a British chemist, professor of chemistry at the University of Dundee . He was elected FRS in 1964. He was educated at Loughborough Grammar School.
Walsh diagrams were first introduced in a series of ten papers in one issue of the Journal of the Chemical Society . Here, he aimed to rationalize the shapes adopted by polyatomic molecules in the ground state as well as in excited states, by applying theoretical contributions made by Mulliken .
Electrochemistry,Electrolytic and Metallic Conduction,Specific Resistance or resistivity (ρ),Specific Conductance or Conductivity (κ),Equivalent Conductance (Λ), Molar Conductance (Λm),Variation of Conductance with Dilution,Debye-Hückel-Onsager Equation,Kohlransch’s Law of Independent Migration of Ions,Faraday’s Laws of Electrolysis,Electrochemical Cells,The Nernst Equation,Oxidation Number
Oxidation Number / State Method For Balancing Redox Reactions,Half-Reaction or Ion-Electron Method For Balancing Redox Reactions,Half-Reaction or Ion-Electron Method For Balancing Redox Reactions,Common Oxidising and Reducing Agents
Ionic equilibria: ph, determination of ph of different acids and bases, salt solutions and
buffers. Titration curves of acids and bases and indicators.
Neutralization curves in acid base analytical titrations, indicators.nehla313
Neutralization curves in acid base analytical titrations, indicators,
strong acid strong base
weak acid strong bse
strong acid weak base
weak acid and weak base
Ionic equilibria: ph, determination of ph of different acids and bases, salt solutions and
buffers. Titration curves of acids and bases and indicators.
In chemistry, pH (potential of hydrogen) is a numeric scale used to specify the acidity or basicity of an aqueous solution. It is approximately the negative of the base 10 logarithm of the molar concentration, measured in units of moles per liter, of hydrogen ions.
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2. Acid
Chemical Substance having characteristics:-
(1) pH < 7
(2) Nutralize base/Alkali
(3) Red Litmus change to blue
Base
Chemical Substance having characteristics:-
(1) pH > 7
(2) Nutralize Acid
(3) Blue Litmus to red
3. •
The Arrhenius Model
Acid – produces hydrogen ions in aqueous solution
Base – produces hydroxide ions in aqueous solution
4. The Bronsted-Lowry Model
Acid – proton donor
Base – proton acceptor
The general reaction for an acid dissolving in water is
6. pH
pH is a measure of the acidity or basicity of an aqueous
solution.
pH Scale:-
7. Indicator
Is organic dye or molecule which indicates
the end point of titration by changing colour of
solution under examination.
Example:-
Phenolphatalene / Methyle blue are
suitable indicators for titration of strong acid &
base.
8. The indicator solution contain both the yellow
In- and the red HIn molecules. The actual
colour shade of the indicator depends on the
ratio of concentration of In- and Hin present
in solution. From the equlibrium constant
expression (1) we can write
[H+] = Kin [In-]/[Hin] ……(2)
Relation of indicator colour to pH
9. If [H+] is large, the concentration of In- ions is
alos large and the colour is yellow. When [H+]
is small,[HIn] is large and the solution is red .
At the equivalence point, [In] = [Hin] and the
colour is orange (red+yellow).
indicator colour is controlled by
hydrogen ion concentration or pH of the
solution.
10. Taking logarithims and using definnition of pH
and kin,the experession (2) can be converted to
Henderson Hasselbalch equation.
pH = pkin log[In]/[Hin] ………..(3)
At the equation point, [In-] = [Hin] and metyl
orange in solution is orange. Then,
pH = pkin
11. The numerical value of the indicator constant
kin for the indicator constant kin for methyl
orange is 3.6 and pH of the orange solution is ,
therefor, about 4. As the value of kin for the
various indicators are different, the will have
intermediate intense colour (middle tint) at
different pH values.
12. When a base is added to an acid solution in a
titration, the colour change of of the indicator is
gradual. It just becomes visible to the human eye
when [in -]/[Hin] = 10 when pH is4.4.
The range between 3.1 (red) and 4.4 (yellow) is
called the colour change interval of methyl orange
. The visible indicator colour colour change takes
place between these values.
13. Indicator Action of Phenolphthalein.
It can be explained as in case of methyl orange. It is a
weak acid exists as the following equilibrium in
solution,
HIn H+ + In-
Colourless Pink
14. HIn molecules are colourless, while In- ions
are pink.Thus in acid solution, phenolphthalein
is colourless and in basic solution it is pink.
The value of kin = 9.6 and the pH of the
intermediate intense pink tint is also 9.6.The
colour change interval of phenolphathalein is
8.1- 10.0.
15. The Ostwald’s theory takes care of the
quantitative aspect of indicator action
adequately. The quinonoid theory, on the other
hand, tell us the cause of colour change of an
indicator in acid-base solution. It lays down
that :
16. The unionised HIn molecule and the anion In-
are tautomeric form of the indicator which is an
organic dye.
One tautomeric form possesses the quinonoid
structural unit and is called the quinonoid
form.
Quinonoid
structure
17. It has a deep colour. The form has a lesser
colouring group,say, -N = N – and or simply
benzene rings and is called the benzenoid form.
This form has a light colour or no colour.
The colour change of the indicator occurs
when one tautomeric form is transformed into
the other due to the change of pH of the
solution.
18. Let us illustrate the quinonoid theory by taking
example of methyl orange and phenolphthalein.
Methyl orange.
The red quinonoid form of methyl orange
exists in acid solution. It is converted to yellow
benzenoid form when pH alters to the basic
side.
20. Phenolphthalein.
Phenolphthalein exists in two
tautomeric forms : (i) the benzoid form
which is yellow and present in basic
solution; and (ii) the quinonoid form
which is pink and present in acid solution.