CHEMISTRY
CHEMISTRY
CHEMISTRY
1. INTRODUCTION
2. FACTORS AFFECTING
RATE OF REACTION
3. EXPERIMENTAL METHODS
4. CHANGE IN
CONCENTRATION WITH
TIME
EXPERIMENTAL METHODS :-
The experimental determination of reaction rates involves
measuring how the concentrations of reactants or products
change over time. For example, the concentration of a reactant
can be measured by spectrophotometry at a wavelength where
no other reactant or product in the system absorbs light.
1. FAST REACTION:-
For faster reactions, the time required to mix the reactants and
bring them to a specified temperature may be comparable or
longer than the half-life of the reaction. Special methods to
start fast reactions without slow mixing step include.
Stopped flow methods, which can reduce the mixing time to
the order of a millisecond. Chemical relaxation methods such
as temperature jump and pressure jump, in which a pre-mixed
system initially at equilibrium is perturbed by rapid heating or
depressurization so that it is no longer at equilibrium, and the
relaxation back to equilibrium is observed. For example, this
method has been used to study the neutralization H3O+ +
OH− with a half-life of 1 μs or less under ordinary conditions.
• Flash photolysis, in which a laser pulse produces
highly excited species such as free radicals, whose
reactions are then studied.
2. EQUILIBRIUM:-
While chemical kinetics is concerned with the rate of a
chemical reaction, thermodynamics determines the extent to
which reactions occur. In a reversible reaction, chemical
equilibrium is reached when the rates of the forward and
reverse reactions are equal and the concentrations of the
reactants and Products no longer change.
3. FREE ENERGY:-
In general terms, the free energy change (ΔG) of a reaction
determines whether a chemical change will take place, but
kinetics describes how fast the reaction is. A reaction can be
very exothermic and have a very positive entropy change but
will not happen in practice if the reaction is too slow. If a
reactant can produce two different products, the
thermodynamically most stable one will in general form,
except in special circumstances when the reaction is said to be
under kinetic reaction control.
The kinetic isotope effect is the difference in the rate of a
chemical reaction when an atom in one of the reactants is
replaced by one of its isotopes.
CHANGE IN CONCENTRATION WITH TIME:-
A rate law simply tells you how the rate of reaction changes
as reactant concentrations change.
COLLISION THEORY
• Collision theory used to predict the
rates of chemical reactions, particularly
for gases.
• Collision theory used to predict the
rates of chemical reactions,
particularly for gases.
• Rate constants use to vary with
temperature.
• Consequently, the actual rate of a
reaction is significant temperature
dependent.
• The rate dependence on temperature
can by explained by the “Collision
Theory “.
• The collision theory assumes that for a
reaction to occur, reactant molecules
must collide with enough energy and
the proper orientation.
• The minimum energy of collision
required for two molecules to react is
called Activation Energy .
• CONCLUSION:-
The main aspects summarized in this presentation were:
• The different ways of expressing chemical reaction
rates.
• The factors that affects the rate of chemical
reactions
• The form and meaning of a rate law including the
ideas of reaction order and rate constant .
• The branch of physical chemistry that is concerned
with understanding the chemical rates .
• Factors affecting the rate of reaction:-
1. Nature of reactant.
2. Physical state.
3. Surface area of solids.
4. Concentration.
5. Temperature.
6. Catalyst.
7. Pressure.
8. Presence of light .
• Experimental methods:-
1. Fast reaction
2. Equilibrium
3. Free energy
• Collision theory:-
Collision theory used to predict the rates of chemical
reactions, particularly for gases. Collision theory used to
predict the rates of chemical reactions, particularly for
gases.
➢ BIBLLIOGRAPHY:-
• WWW.WIKIPEDIA.COM
• WWW.PEDRO JULIO.COM
• WWW.BRITANNICA.COM
• WWWCHEMGUIDE.COM