Reaction energy profile graph. Phase equilibria
The enthalpy change DH is essentially the difference between the bond energies of reactants and products, including conjugation, stress, and solvation energies. DH can be calculated by summing the energies of all the bonds that break during the reaction and subtracting from them the sum of the energies of all the bonds formed, adding all changes in conjugation, stress, and solvation energies. In addition, the change in enthalpy can be determined experimentally by measuring the thermal effect of the reaction, since the change in enthalpy is equal to the heat of the reaction, taken with the opposite sign.
- DH=Qp
The change in entropy DS characterizes the degree of disorder of the system. In organic chemistry, this factor rarely plays a big role, because. reactions proceed at relatively low temperatures, at which the entropy factor is small. However, in some cases, the change in entropy can play a significant role:
Since gases have a higher entropy than liquids (especially than solids), then any reaction in which the starting materials are liquid or solid, and one or more products are gaseous, is thermodynamically favorable, since the entropy of the system increases;
If during the reaction more molecules of products are formed than molecules of the starting substances, then the reaction proceeds with an increase in entropy.
By itself, a negative DG value does not mean that the reaction will proceed in a foreseeable period of time. The negative value of the change in free energy is a necessary but not sufficient factor for the spontaneous occurrence of a chemical reaction. For example, the reaction of two moles of hydrogen with one mole of oxygen, proceeding with the formation of water, is characterized by a large negative change in free energy. However, a mixture of O 2 and H 2 can be stored for decades at room temperature without any sign of a chemical reaction.
Mechanisms of organic reactions
Knowledge of their mechanisms is extremely useful for understanding organic reactions.
Reaction mechanism - a detailed description of the process of transformation of starting compounds into products. The mechanism includes data on the method and sequence of cleavage and formation of bonds, the structure of intermediates (intermediate products), kinetics, thermodynamics, and stereochemistry of the reaction. The mechanism should not contradict the existing experimental facts, and when new ones appear, they should also explain them.
When considering the subtle features of mechanisms, it is extremely useful to use the so-called energy diagram (energy profile) reactions. This is a graphical dependence of the energy of the system on the complex function of the distance between the reacting substances, which is usually called " reaction coordinate" or " the course of the reaction» (Figure 3.1).
Rice. 3.1. Energy diagram: A - endo-, B - exothermic reaction.
This figure illustrates the flow of one-step reactions. An endothermic reaction takes place with the absorption of heat, an exothermic reaction with release.
Almost all chemical reactions occur when two or more, which is very rare, reacting particles collide. From fig. 3.1 it can be seen that the approach of the reacting molecules leads to an increase in the energy of the system up to a certain maximum. Collisions will be effective when the reacting substances have some excess energy compared to the average energy of the molecules in the system. Particles that do not have such an excess of energy after a collision scatter in different directions. Activation energy- excess energy required to overcome the energy barrier. The maximum energy of the system (the highest point of the energy diagram) corresponds to transition state (activated complex). It is the presence of the transition state that explains the reason that even exothermic reactions usually do not occur spontaneously, but only when heated or other ways of activating the system.
It is the transition state - the highest energy point of the reaction - that determines the course of the entire transformation. Knowledge of its structure can clarify the mechanism of chemical transformation. However, the lifetime of the activated complex is so short that there are no physical methods to register it and, consequently, to obtain knowledge about its structure.
J. Hammond's postulate
To indirectly estimate the structure of the transition state, one uses postulate by J. Hammond (1955): insignificant energy changes are accompanied by minor changes in the molecular structure. More clear wording: the structure of the transition state is similar to the structure of those substances to which it is closer in energy. In exothermic reactions, the transition state is closer in structure to the starting reactants (Fig. 3.1). Such an activated complex is called early transition state. The transition state in endothermic reactions is closer in structure to the reaction products, it is called late. Similar impacts on similar structures lead to similar results. That's why everything factors that stabilize(energy-lowering states) energetically close to the transition state initial, intermediate or final substance, lower and the energy of the activated complex.
The use of Hammond's postulate is especially useful when considering multi-step reactions (Figure 3.2).
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Fig 3.2. Energy diagram of a two-step reaction
Figure 3.2 shows that the reaction proceeds in two stages, through one intermediate product. The transformation of products into an intermediate (first stage) is of greater importance for the entire reaction than the transformation of an intermediate into reaction products (second stage). This is confirmed by the corresponding activation energies of the first and second stages (Ea 1 and Ea 2, respectively). The entire course of the reaction is determined by its highest energy point - the transition state of the first stage [PS 1]. If Hammond's postulate is applied to this reaction, it is easy to conclude that the intermediate product is energetically closest to the transition states of both stages of the reaction.
Energy profile of the reaction. A + B = AB (no catalyst) A + B + K? + V? ? AB + K (with cat.).
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In total there are 28 presentations in the topic
Collision theory allows you to establish a mathematical relationship between the reaction rate and the frequency of collisions, as well as the probability that the collision energy E exceeds the minimum energy Em necessary for the reaction to occur. This ratio has the form
Reaction Rate = (Frequency of Collisions) (Probability that E > Em) From this relationship, the following equation can be derived:
where k is the reaction rate constant; P-steric factor, having a value from 0 to 1 and corresponding to that part of the colliding molecules that have the necessary mutual orientation during the collision; Z-number of collisions, which is related to the frequency of collisions; Ea is the activation energy corresponding to the minimum collision energy that the reacting molecules must have; L is the gas constant; T is absolute temperature.
The two factors, P and Z, can be combined into one constant A, which is called the pre-exponential factor or the Arrhenius constant. The result is the well-known Arrhenius equation, which we already met in the previous section:
TRANSITION STATE THEORY
The transition state theory considers reacting molecules as a single system. She studies in detail the changes in the geometric arrangement of atoms in this system as the transformation of reactants into products takes place in it. The geometric arrangement of atoms in such a molecular system is called a configuration. As the configuration of the reactants turns into the configuration of products, there is a gradual increase in the potential energy of the system until it reaches a maximum. At the moment when the maximum energy is reached, the molecules have a critical configuration, which is called the transition state or activated complex. Only those molecules that have sufficient total energy can achieve this critical configuration. As the configuration of this transition state turns into the configuration of products, there is a decrease in potential energy (Fig. 9.12). The reaction coordinate in these two diagrams represents the changes in the geometric arrangement of the atoms of the reacting molecules, considered as a single system, as this system undergoes a transformation, starting with the configuration of the reactants, passing into the critical configuration, and ending with the configuration of the products. If intermediates are formed in the reaction, then the appearance of each intermediate corresponds to a minimum on the graph of the dependence of the potential energy on the reaction coordinate (Fig. 9.13).
Rice. 9.12. Energy profile of the reaction - a plot of the potential energy versus the reaction coordinate, a - for an exothermic reaction; b-for an endothermic reaction.
The transition state theory can be used to predict the constants A and El in the Arrhenius equation. The use of this theory and modern computer technology makes it possible to establish an accurate picture of the course of chemical reactions at the molecular level.
The rate of a chemical reaction
and its dependence on various factors
Lesson using information technology
Chemistry can never be learned
not seeing the practice itself and not taking up chemical operations.
M.V. Lomonosov
The restructuring of higher and secondary specialized education in the country, school reform provides for further improvement of the forms, methods and means of education, the use of various technologies, including student-centered learning (LOO), problem-search and computer technologies.
As teachers, we are changing too. In my work I try to constantly use new developments, modern educational technologies.
Recently, a lot of materials have appeared on computer disks. They can be used in the development of essays, writing term papers, with independent work of students. Information technologies allow me to quickly organize training and knowledge testing, compose adaptive programs and apply them in teaching chemistry.
Computer technology and the use of computer technology today act not only as a means of automating all learning processes, but also as a tool for a sharp increase in the efficiency of students' intellectual activity.
I use computer technologies in my lessons for different purposes:
Problem solving, quantitative calculations, data processing (according to the proposed algorithm);
Implementation of self-control and standardized control of knowledge on the content of educational information (test, control differentiated tasks, maps and other questionnaires);
Automation of a chemical experiment, connection with optical equipment (projections of experiments on a screen);
Obtaining the necessary reference data, compiling control, differentiated work, analyzing typical mistakes of students (automated control systems and information banks);
Independent work of students on the development of essays and term papers, work with the material, performance of verification work (getting the result, exercise self-control).
The proposed lesson from the section "Chemical Kinetics" corresponds to the program of the textbook "Chemistry-10" by the authors L.S. Guzey and R.P. Surovtseva. The study of this topic is preceded by the study of thermodynamics of reactions. The proposed material does not correspond to the mandatory minimum content, but primarily to the profile level of education.
The lesson uses group work, a differentiated approach, developing and problem-search technologies, and most importantly, computer technologies for conducting a demonstration experiment, which makes it possible to clearly understand what the rate of a chemical reaction is and how it depends on various factors.
Lesson goals. Update and deepen knowledge about the rate of a chemical reaction; using group work, consider and study on various factors: the nature of the reactants, the surface area of contact of substances, temperature, catalyst; using a computer measuring unit, to clearly demonstrate what the rate of a chemical reaction is and how it depends on the concentration of reactants.
Lesson motto.“There is only that which can be measured” (M. Planck).
Class decoration. The teacher announces the topic of the upcoming lesson in advance, divides the class into four creative groups of 5-6 people, approximately the same in ability. In the previous lesson, students receive homework - to prepare reports on the practical application of the Arrhenius equation and on the types of catalysis.
Equipment and reagents. On the tables of students - textbooks, notebooks, tables, laboratory sheets, racks with test tubes;
group 1: zinc granules, magnesium tape, hydrochloric acid solution;
group 2: glass rod; iron filings, iron nail, copper(II) chloride solution;
group 3: pipette, test tube holder, spirit lamp, matches; copper(II) oxide, sulfuric acid solution;
group 4(performs a demonstration experiment on a demonstration table): a computer with a measuring unit, an optical density sensor at a wavelength of 525 nm, a cuvette, a magnetic stirrer, a 10 ml syringe, a 100 ml graduated cylinder; solutions of potassium iodide KI 1M, potassium persulfate K 2 S 2 O 8 0.1M, distilled water.
All notes during the lesson, students complete in their notebooks.
DURING THE CLASSES
Motivation of the importance of the chosen topic
The teacher begins the explanation of the material with examples of chemical reactions occurring at different rates. Students can give examples of reactions.
Chemical reactions proceed at different rates. Some go slowly, over months, such as the corrosion of iron or the fermentation (fermentation) of grape juice, which results in wine. Others are completed in a few weeks, like the alcoholic fermentation of glucose. Still others end very quickly, such as the precipitation of insoluble salts, and some proceed instantly, such as explosions.
Almost instantly, many reactions in aqueous solutions proceed very quickly:
We mix aqueous solutions of Na 2 CO 3 and CaCl 2, the reaction product CaCO 3 is insoluble in water, it is formed immediately;
We add an excess of acid to an alkaline solution of phenolphthalein, the solution becomes colorless instantly. This means that the neutralization reaction, the reaction of turning the colored form of the indicator into a colorless one, proceeds very quickly.
Rust forms slowly on iron objects. On copper and bronze objects, corrosion products of black-brown or greenish color (patina) slowly form. The speed of all these processes is different.
Updating views
about the rate of chemical reactions
Chemical reactions are one of the most important concepts in chemistry. For their understanding and competent use in the educational process, the teacher needs to know and be able to explain the main characteristics of any chemical reaction: thermal effect, equilibrium, speed. Chemical thermodynamics makes it possible to predict in which direction a particular chemical reaction can spontaneously proceed, but chemical thermodynamics alone does not answer the question of how and at what rate the reaction will proceed. The concept of the rate of a chemical reaction is one of the basic concepts in chemical kinetics.
To study new material, students use the necessary knowledge about the rate of a chemical reaction, the stage of updating knowledge is going through. But this concept is deepened by the concepts of the rate of homogeneous and heterogeneous reactions, activation energy, the Arrhenius equation is introduced - this is the zone of proximal development of students (see Appendix No. 1 "The structure of the problem-search activity of the teacher and students ...").
What is meant by reaction rate? How can it be measured and changed? To answer these questions will help the science that studies the patterns of reactions in time - chemical kinetics.
Recall the basic concepts and patterns used in kinetics (the students answer and the teacher supplements).
Chemical kinetics is a branch of chemistry whose task is to explain the qualitative and quantitative changes in chemical processes that occur over time. Usually this general task is divided into two, more specific ones:
1) identification of the reaction mechanism - the establishment of the elementary stages of the process and the sequence of their course (qualitative changes);
2) quantitative description of a chemical reaction - the establishment of strict ratios that allow you to calculate changes in the amounts of initial reagents and products as the reaction proceeds.
The basic concept in chemical kinetics is the concept of the reaction rate. The rate of a chemical reaction is determined by the amount of a substance that has reacted per unit of time in a unit of reaction space.
If the concentration of one of the reactants decreases from With 1 to With 2 for a period of time from t 1 to t 2 , then in accordance with the definition of the reaction rate is (Fig. 1):
The “–” sign on the right side of the equation means the following. As the reaction proceeds ( t 2 – t 1) > 0 the concentration of reagents decreases, therefore, ( c 2 – c 1) < 0, а т.к. скорость реакции всегда положительна, то перед дробью следует поставить знак «–».
Rice. one.
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Quantitatively, the relationship between the reaction rate and the molar concentrations of the reactants is described by the basic law of chemical kinetics - the law of mass action.
The rate of a chemical reaction at constant temperature is proportional to the product of the concentrations of the reactants.
For reaction
a A+ b B = With C + d D,
in accordance with the law of mass action, the dependence of the velocity on the concentrations of reactants can be represented as:
where k is the rate constant; n BUT, n B are the reaction orders for reagents A and B, respectively;
n A+ n B is the general order of the reaction.
In homogeneous reactions, the reactants are in the same gas phase or in solution, uniformly mixed with each other, the reaction proceeds throughout the volume of the mixture. The concentration of the reagent is equal to the quotient of the amount of substance divided by the volume of the mixture: With = /V.
Average reaction rate:
The shorter the time interval, the more accurate the reaction rate will be.
Heterogeneous reactions take place at the phase boundary: gas - solid, gas - liquid, liquid - solid, solid - solid. Speed reaction
measured per unit area of contact of reactants S.
When considering the thermal effects of chemical reactions, the transformation of reactant molecules (A + B) into product molecules (C + D) from a thermodynamic point of view is explained as “climbing an energy mountain” in the case of endothermic reactions (Fig. 2, a) or "downhill" for exothermic reactions (Fig. 2, b).
Reactant molecules, in order to react, must first stock up on additional energy in order to overcome the energy barrier on the way to the reaction products. It is significant that such a barrier also exists in the case of exothermic reactions, so that instead of simply “sliding down the hill”, the molecules have to “climb up the hill” first.
Rice. 2.
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The driving force of the reaction is the desire to reach a minimum of energy.
In order for a reaction to proceed, the particles of the reactants must collide with each other. As the temperature rises, the number of these collisions increases due to the increase in the kinetic energy of the molecules, so the reaction rate increases. But not every collision of molecules of reacting substances leads to their interaction: for the interaction of molecules, the bonds between atoms in them must become weaker or break, for which a certain energy must be expended. If the colliding molecules do not have this energy, their collision does not lead to a reaction. The excess energy that molecules must have in order for their collision to lead to the formation of molecules of a new substance is called activation energy this reaction E a, usually measured in J / mol, kJ / mol. Molecules with this energy are called active molecules.
On fig. 3 shows energy profiles:
a) endothermic reaction, + H = –Q,
N 2 + O 2 2NO - Q;
b) exothermic reaction, - H = +Q,
H 2 + I 2 2HI + Q.
During the reaction, chemical bonds in active molecules weaken and new bonds arise between the particles of the reacting substances, a transition state is formed - an activated complex, when old bonds are not completely destroyed, and new ones have already begun to be built. Activation energy is the energy required for the formation of an activated complex. The energy barrier is different, the lower it is, the easier and faster the reaction.
The point at the top of the energy barrier is called transition state. From this point, the system can freely pass into the reaction product or return to its original state (Fig. 4).
The activation energy is the factor by which the nature of the reactants affects the rate of a reaction. For some reactions it is small, for others it is large. If the activation energy is small (< 40 кДж/моль), то большая часть столкновений между молекулами реагирующих веществ приводит к реакции. Скорость таких реакций велика. Если энергия активации велика (>40 kJ / mol), then in this case only a small part of the collisions of molecules or other particles leads to a reaction. The rate of such a reaction is low.
The reaction rate at a given moment of time can be calculated if the number of active collisions of reacting particles per unit time is known. Therefore, the dependence of the reaction rate on temperature can be written as:
0 exp(- E a / RT),
where 0 is the reaction rate, provided that each collision leads to an interaction ( E a = 0). This expression for the reaction rate is − Arrhenius equation- an important equation in chemical kinetics (see Appendix No. 2 for its practical application, students make reports).
Why do chemical reactions proceed at different rates? This is the main question that faces the teacher and the guys in the lesson. Students answer it theoretically by conducting laboratory experiments in groups and solving problems.
Group work
The work of the groups includes the following activities:
Experimental study of factors affecting the rate of a chemical reaction;
Observation and analysis of the obtained results of experiments;
Filling out laboratory sheets reflecting the progress of work and conclusions.
A prerequisite for successful work in groups and the implementation of the tasks set is the provision of each student’s workplace with the necessary equipment, visual aids. During the work, the teacher approaches all groups, if necessary, provides advisory assistance. The content of tasks for the work of each of the groups is disclosed below.
Laboratory experience No. 1.
The dependence of the rate of a chemical reaction
from the nature of the reactants
Target. To consolidate the concept of "the rate of a chemical reaction" and to reveal its dependence on the nature of the reacting substances.
Equipment and reagents. Stand with test tubes; zinc granules, magnesium tape, hydrochloric acid solution.
Demonstration experience.
Reaction rate and its dependence
from the concentration of starting substances
Target. Demonstrate clearly what the rate of a chemical reaction is and how it depends on the concentration of the starting substances.
Equipment and reagents. Computer with measuring unit, optical density sensor at wavelength = 525 nm, cuvette, magnetic stirrer, 5 ml syringe, 100 ml graduated cylinder; solutions - 1M KI, 0.1M K 2 S 2 O 8, distilled water.
Chemical nature of the process. The reaction of oxidation of iodide ion with persulfate is investigated:
2I – + S 2 O 8 2– = I 2 + 2SO 4 2– .
The reaction is carried out in excess of potassium iodide. The released iodine turns the solution brown. The concentration of iodine is determined by the color intensity of the solution using an optical density sensor at 525 nm.
Preparation for work. An optical density sensor tuned to a wavelength of 525 nm is connected to the first channel of the measuring unit. Turn on the sensor in the time-dependent mode, pour 10 ml of 1M KI solution and 90 ml of distilled water into the cuvette. Set up the sensor.
Performance. Start the mixing process. Take 5 ml of K 2 S 2 O 8 solution into the syringe, quickly pour it into the cuvette, simultaneously starting the measurement process by pressing the “Start” screen button. The measurement is stopped when the optical density reaches 0.5.
The experiment is repeated using 20 ml of KI solution and 80 ml of water.
Comments. The rate of a reaction is the change in the concentration of reactants or reaction products per unit time. The reaction rate depends on the concentration of the initial reagents at a given time.
inferred concepts. Reaction rate, its dependence on concentration.
Conclusions. Since the reactants are consumed during the course of the reaction, the rate slows down.
With an increase in the concentration of the initial reagent, the reaction rate increases. Moreover, in this case, with a doubling of the concentration, the reaction rate also doubled.
Laboratory experience number 2.
Effect of temperature on speed
Target. To consolidate the concept of "the rate of a chemical reaction" and to investigate the effect of temperature on the rate of a chemical reaction.
Equipment and reagents. Stand with test tubes, pipette, spirit lamp, test tube holder; copper(II) oxide, sulfuric acid solution (1:3).
Laboratory experience number 3.
The dependence of the rate of a chemical reaction
from the area of the contact surface
reactants
Target. To consolidate the concept of "the rate of a chemical reaction" and to reveal its dependence on the size of the contact surface of the reactants.
Equipment and reagents. Stand with test tubes, glass rod; iron filings, iron nail, copper(II) chloride solution.
Presentation of the results of group work, their discussion
The order in which the results are presented is determined by the group numbers (in turn). Students speak at the blackboard using tables filled out according to the results of laboratory experiments. A brief discussion of the results of the work of the groups is organized, conclusions are formulated. The teacher points out another factor that affects the rate of a chemical reaction - the presence of a catalyst.
Catalysts are substances that speed up a chemical reaction inhibitors are substances that slow down a chemical reaction. The catalysts and inhibitors themselves are not consumed in the reaction and are not part of the reaction products.
Catalysis is the process of changing the rate of a reaction under the action of a catalyst. The action of the catalyst is selective. Reactions that take place with the participation of a catalyst are called catalytic reactions.
M echanism
Often reactions are slow because their activation energy E and is large (Fig. 5):
A + B A B AB.
The catalyst (K) speeds up the reaction:
Activation energies E"a and E"" a are small, so the reactions proceed quickly.
With the participation of a catalyst, there is a decrease E a, an energy gain is formed and the reaction proceeds faster.
V i d y k a t a l i z a
1. homogeneous catalysis– initial substances and catalyst – single-phase system.
For example, natural fluctuations in the thickness of the Earth's ozone layer are associated with changes in solar activity. In the upper atmosphere, the ozone layer is destroyed, catalyzed by nitrogen oxides:
2. heterogeneous catalysis– the initial substances and the catalyst form a different-phase system.
The mechanism of heterogeneous catalysis includes five stages:
Diffusion - reacting molecules diffuse to the surface of the catalyst;
Adsorption - reactants accumulate on the surface of the catalyst;
Chemical reaction - the surface of the catalyst is not uniform, there are active centers on it, they weaken the bonds between atoms in the adsorbed molecules, the reacting molecules are deformed, sometimes break down into atoms, which facilitates the chemical reaction;
Desorption - product molecules are first held by the catalyst surface, then released;
Diffusion - product molecules diffuse from the surface of the catalyst.
Figuratively speaking, the mechanism of the catalyst can be compared with the passage of tourists through a mountain pass. Tourists unfamiliar with the terrain will choose the most obvious but most difficult route, requiring a long ascent and descent over the top of the mountain. An experienced guide (catalyst) will lead his group along the path, bypassing the top. Although this path is winding, but less difficult, it is easier to reach the final point along it, after which the guide returns to the starting point.
Catalysts operating in living organisms constitute a special group. Such catalysts are called enzymes or enzymes.
Enzymes (enzymes)- these are protein molecules that accelerate chemical processes in biological systems (there are about 30 thousand different enzymes in the body, each of them accelerates the corresponding reaction).
Demonstration experience.
Catalytic decomposition of hydrogen peroxide
(conducted by the teacher)
2H 2 O 2 2H 2 O + O 2 .
Pour 5 ml of a pharmacy solution of hydrogen peroxide into three test tubes. The first test tube is a control tube, for comparison, a piece of raw meat is lowered into the second test tube with tweezers, and a piece of raw carrot is placed into the third test tube. Boiling is observed in two test tubes, except for the first one. Smoldering splinters are introduced into the second and third test tubes, which flare up, because. oxygen is released. The teacher explains that the decomposition of hydrogen peroxide occurs without a catalyst, but much more slowly. The reaction may take several months. Fast reactions in other test tubes demonstrate the work of an enzyme - catalase, which is found in both plant and animal cells.
The efficiency of the catalase enzyme can be illustrated by data on the decomposition of H 2 O 2 in an aqueous solution.
In more detail, they get acquainted with enzymes when studying the course of chemistry of the 11th grade.
With a demonstration experiment, the upbringing of sustained attention, the ability to observe experience, analyze, and draw conclusions begins. The group form of work allows you to effectively acquire knowledge, cultivating a sense of collectivism.
The use of a set of equipment with a computer measuring unit and sensors (temperature, optical density, electrical conductivity, pH level) significantly expands the possibilities of a demonstration experiment, because allows you to look inside the process, which previously, studying this topic only theoretically, we could not do. The study of quantitative patterns is one of the key and most complex topics in chemistry (see Appendix No. 3 "Parameters that are used in quantitative chemical calculations").
In this lesson, we are interested in the parameters of the reaction. In previous lessons, students got acquainted with thermodynamic parameters, and the parameters of matter and medium will be studied in subsequent lessons.
Lesson summary, reflective analysis
The teacher summarizes the lesson. Students fill out the student's work control sheets, on which they indicate the class, last name, first name, evaluate their work in the lesson, the work of the group, understanding the topic (“bad”, “good”, “excellent”).
Students answer to questions.
1. With what mood do you leave the lesson?
2. What is interesting about the lesson for each group and each student?
3. What is the use of this lesson for you?
4. What difficulties did you face in the lesson?
Different classes ask different questions. From experience, we can say that at the reflective stage, students give a high assessment of the lesson (“5”, less often “4”), note the unusualness, clarity, richness of the lesson, a high emotional level, logic, and interesting information material. The technology of cooperation between teacher and students is the most important in the lesson. Together, common goals are achieved, students learn the material better and apply the knowledge gained.
Homework
Along with the paragraphs of the textbook, each group receives an individual task to study the influence of a particular factor on the rate of a chemical reaction.
Task 1. At t= 30 °С the reaction proceeds in 25 min, and at t= 50 °С - in 4 min. Calculate the temperature coefficient of the reaction.
Task 2. The interaction of aluminum with chlorine proceeds according to the equation:
2Al (solid) + 3Cl 2 (g) = 2AlCl 3 (solid).
The initial concentration of chlorine is 0.05 mol/l. Reaction rate constant 0.2 L/(mol s).
Write a mathematical expression for the reaction rate. How does the reaction rate change compared to the initial one if the pressure in the system is increased by 6 times?
Task 3. Decomposition reactions with the formation of oxygen and hydrogen were carried out in two identical vessels. For 10 s, 22.4 l of O 2 were obtained in the first vessel, and 4 g of H 2 in the second. Which chemical reaction has the highest rate? How many times?
Task 4. Suggest ways to increase the reaction rate by 16 times by changing the concentrations of the starting substances:
a) 2Cu (tv.) + O 2 (g.) \u003d 2CuO (tv.);
b) 2H 2 (g.) + O 2 (g.) \u003d 2H 2 O (g.).
A feature of the lesson is that it offers material that goes beyond the scope of the textbook. This is necessary both to improve general erudition and for future applicants. Additional material in the profile class is based mainly on the materials of entrance exams to various universities.
The purpose of pedagogical technologies is to increase the efficiency of the educational process. The main thing in any technology is a focus on the personality of the student. Pedagogical technology is a set of interrelated means, methods, processes necessary for a targeted impact on the formation of a personality with given qualities. I use a student-centered approach in my lessons. As a result, students manage to approach the study of the material more consciously and creatively. It is the technology of cooperation between teacher and student that is important in achieving high results. The active use of elements of pedagogical technologies in the classroom contributes to the development of the student's motivational sphere, intelligence, independence, the ability to control and manage their educational and cognitive activities.
My subject is chemistry, but I also teach human studies. The use of new approaches in education allows you to look at your subject differently. The main thing is to see a person in every student.
Chemistry is the science of substances. I approach the study of substances not only from the point of view of their practical significance for society, but also from the position of philosophical understanding of the world. In the lessons of chemistry and human studies, I show the integrity of the world and man, I try to reveal to children the infinity and harmony of life, to cultivate the desire to understand and know oneself, the desire to improve oneself, to work on oneself in order to improve life. I am pleased with the interest of the guys in these problems. And I think it's good for us as teachers to reflect on this. Only by improving and developing ourselves, we can teach children.
APPENDIX No. 1
The structure of the problem-search activity of the teacher and students
on the study of the properties of substances and the essence of chemical reactions
(possible use of information technology)
APPENDIX No. 2
Practical use of the Arrhenius equationExample 1 The speed (frequency) of cricket chirping obeys, although not quite strictly, the Arrhenius equation, gradually increasing in the temperature range from 14.2 °C to 27 °C, with an effective activation energy E a = 51 kJ/mol. By the frequency of chirring, you can accurately determine the temperature: you need to count their number in 15 seconds and add 40, you get the temperature in degrees Fahrenheit (F) (Americans still use this temperature scale).
So, at 55 F (12.8 ° C), the chirring frequency is 1 str. / s, and at 100 F (37.8 ° C) - 4 str. / s.
Example 2
In the temperature range from 18 °C to 34 °C, the heart rate of the sea turtle is consistent with the Arrhenius equation, which gives the activation energy
E a = 76.6 kJ/mol, but at lower temperatures the activation energy increases sharply. This may be due to the fact that at lower temperatures the turtle does not feel very well and its heart rate begins to be controlled by other biochemical reactions.
Example 3
Particularly interesting are the attempts to “put on Arrhenius dependence” the psychological processes of a person. So, people with different body temperatures (from 36.4 ° C to 39 ° C) were asked to count seconds. It turned out that the higher the temperature, the faster the score
(E a = 100.4 kJ/mol). Thus, our subjective sense of time obeys the Arrhenius equation. The author of the sociological study, G. Hoagland, suggested that this is due to some biochemical processes in the human brain.
The German researcher H. von Ferstler measured the rate of forgetting in people with different temperatures. He gave people a sequence of different signs and measured the time during which people remembered this sequence. The result was the same as Hoagland's: an Arrhenius dependence with E a = 100.4 kJ/mol.
These examples show that many processes in nature, including psychological ones, obey the Arrhenius equation with rather high values of activation energy E a. The last remark is especially important because E and physical processes (for example, viscous fluid flow) usually does not exceed 20 kJ/mol. A high activation energy generally means that chemical bonds are being broken. So in all the analyzed examples, undoubtedly, real chemical reactions (obviously, enzymatic ones) take place.
APPENDIX No. 3
The theory was formulated by S. Arrhenius in 1889. This theory is based on the idea that for a chemical reaction to occur, a collision between the molecules of the initial substances is necessary, and the number of collisions is determined by the intensity of the thermal motion of the molecules, i.e. temperature dependent. But not every collision of molecules leads to a chemical transformation - only active collision leads to it.
The activation energy is a characteristic of each reaction and determines the influence on the rate of a chemical reaction of the nature of the reactants.
Arrhenius equation:
Energy profile of exo- and endothermic reaction
Exothermic reaction - with the release of heat.
CH 4 (g) + 2O 2 (g) \u003d CO 2 (g) + 2H 2 O (g) + Q
Endothermic - with the absorption of heat. CaCO 3 (cr) \u003d CaO (cr) + CO 2 (g) - Q,
Catalysis. The concept of homogeneous and heterogeneous catalysis. Catalysts positive and negative
The phenomenon of catalysis is a change in the rate of a reaction under the action of certain substances, which by the end of the reaction remain chemically unchanged.
The homogeneous catalyst and reactant form one phase.
Heterogeneous catalyst and reactant are in different phases
Distinguish positive catalysis(acceleration of reactions) and negative catalysis(reaction slowdown)
Energy profile of a catalytic reaction
The concept of enzymatic catalysis. Features of the catalytic activity of enzymes
Enzymatic catalysis- catalytic reactions occurring with the participation of enzymes - biological catalysts of protein nature. Enzymatic catalysis has two characteristic features: 1) high specificity 2) high activity
The catalytic activity of an enzyme can most accurately be expressed using a measure called molar activity, which is measured in katals per 1 mol of enzyme (cat × mol -1 f.). This indicator shows how many substrate molecules are converted in 1 second by one enzyme molecule.
Reversible and irreversible in the direction of the reaction
Reversible reactions- chemical reactions occurring simultaneously in two opposite directions (forward and reverse), for example:
3H 2 + N 2 ⇆ 2NH 3
irreversible called such chemical processes, the products of which are not able to react with each other with the formation of starting substances. Examples of irreversible reactions are the decomposition of Berthollet salt when heated
2KSlO3 > 2KSl + 302,
Chemical equilibrium constant. Thermodynamic equilibrium conditions in thermodynamic systems
The equilibrium constant is the ratio of the products of the concentrations of the reaction products to the product of the concentrations of the starting substances
Thermodynamic equilibrium- the state of the system, in which the macroscopic quantities of this system (temperature, pressure, volume, entropy) remain unchanged in time under conditions of isolation from the environment.
Diffusion
diffusion is the mixing of molecules of a substance during their random thermal motion.
the process of mutual penetration of molecules or atoms of one substance between the molecules or atoms of another, leading to spontaneous alignment of their concentrations throughout the occupied volume
examples: 1) dissolving milk in coffee;
2) brewing tea;
3) the spread of odors;
Osmosis. Endo-exoosmosis
Osmosis is the result of the inequality of the chemical potentials of water on opposite sides of the membrane. An ideal semi-permeable membrane allows water molecules to pass through but does not allow solute molecules to pass through.
One-way diffusion of a solvent through a semi-permeable membrane that separates the solution from the pure solvent.
are observed when fluids come into interaction through the membranes.
ENDOOSMOS biol. the process of seepage (diffusion) of liquids and certain solutes from the external environment into the cell
EKZOOSMOS biol. the process of seepage (diffusion) of liquids and certain solutes from the cell into the surrounding environment
Osmosis, directed inside a limited volume of liquid, is called endosmosis, out - exosmosome.
22. Osmotic pressure (van't Hoff's law)
The osmotic pressure is equal to the pressure that the solute would have if it were in a gaseous state in the bulk of the solution.
