Chemical Equilibrium And Ph Biology Essay

Chemical Equilibrium And Ph Biology EssayIn a chemical process, chemical is a state in which cocentration of reactants and the tautness of crossings does non change overtime i.e when the forward reception proceeds at the akin rate as backward reaction and it exists in dynamic equilibrium.The laws of chemical equilibrium define the direction in which a chemical reaction allow for proceed, as well as the quantities of reactants and products that will remain after the reaction comes to an end. An understanding of chemical equilibrium and how it can manipulated is essential for anyone involved in interpersonal chemistry and its applications. The fundamental equation provides the basis for understanding chemical equilibrium.pH is Quantitative measure of stength of acidity and alkalinity of solution. When the concentration of H+ and OH- ions in aqueous solution ar frequently very small numbers and there fore inconvenient to work with, Soren Sorensen in 1909 proposed a more practical measure called pH. It is defined as the negative of the hydrogen ion concentration.pH= -logH+.Acidic and basic ar two extremes that describe a chemical property chemicals. Mixing acids and bases can cancel verboten or neutralize their extreme effects. A pith that is neither acidic nor basic is neutral.The pH scale measures how acidic or basic a substance is. The pH ranges from 0 to 14. A pH of 7 is neutral. A pH less than 7 is acidic. A pH greater than 7 is basic.HISTORY-The plan of chemical equilibrium develop after Berthoket (1803) found that some chemical are reversible. For any reaction to be equilibrium, rate of forward reaction is have-to doe with rate of backward reaction, so at equilibrium nearly all the reactant are used up for to left it hardly any product make from reactant.In 1864 Guldberg and waage showed experimentally that in chemical reactions an equillibrium is reached that can be approached from either direction. They were apparently the first to realize t hat there is a mathematical relation betwixt the concentration of reactants and products at equillibrium. In 1877 vant hoff suggested that in the equillibrium expressions the concentrationof each reactant should appear to the first power, corresponding with the stochiometric numbers in the balanced chemical equation.The belief of pH was first introduced by Soren Peder Lauritz Sorensen at the carlsberg laboratory in 1909 and revised to the modern pH in 1924 after it became apparent that electromotive force in cells depended on drill rather than concentration of hydrogen ions.TYPES OF EQUILLIBRIUM-Physical equillibrium- Equillibrium between two phases of the same substance is called Physical equillibrium because the changes that occur are physical processes.e.g The vaporization of water in a closed container at a precondition temperature is an compositors case of physical equilibrium. In this instance the number of H2O molecules leaving and the number of returning to the unruffl ed phase are equal.H2O(l) = H2O(g)The study of physical equilibrium Yields useful information such as the equilibrium vapour pressure. If a reaction is-aA + bB = cC + dDwhere a, b, c and d are the stoichiometric coefficients for the reacting species A, B, C , and D. For the reaction at a particular temperatureK = (C)C (D)d(A)a (B)bwhere K is the equilibrium continuous.This equation was formulated by cato Guldberg and Petr occupy in 1864. It is the mathematical expressions of their law of mass of action, which holds that for a reversible reaction at equilibrium and a constant temperature, a certain ratio of reactant and product concentration has a constant value K. and the equilibrium constant does depend on the volume, concentration, catalyst, pressure e.t.c. It only depends upon temperature.The equilibrium constant ,then, is defined by a quotient, the numerator of which is obtained by multiplying together the equilibrium concentration of the products, each raised to a power equal to its stoichiometric coefficient in the balanced equation denoted by Q.If Q If Q K then reaction takes backward reaction.If Q = K then reaction is at equilibrium state.The magnitude of equilibrium constant tells whether the reaction favors the products or reactant.If K 1 , the equilibrium will lie to the right and favours the products.If K Homogeneous equillibrium- The term homogeneous equilibrium applies to reactions in which all reacting species are in the same phase.E.g An example of homogenous gas phase equilibrium is the dissociation of N2O4.N2O4 (g) = N2O4 (g)aA(g) = bB(g)then, Kc = (B)b/(A)athe concentrations of reactants and the products in gaseous reaction can also be expressed in basis of their partial pressures. At constant temperature the pressure P of gas is presently related to the concentrations in mol/ L of the gas. i.e P =(n/V)RT.And the expressions can be given by Kp = PbB/PaA where Pa and P b are the partial pressure of A and B. After substiuting these relat ions in to the expressions, we getKp=Kc(RT)b-aIf b-a is equal to zero, then reaction is at equilibrium.If b-a 0 , then backward reaction is favourable.If b-a Heterogeneous equilibrium- A heterogeneous equilibrium results from a reversible reaction and products that are in different phases.e.g when calcium carbonate is heated in a closed vessel, the following equilibrium is attained.CaCO3(S = CaO(S) + CO2If a reaction aA(S) + bB(s) = cC(s) + dD(g),the concentration of a straightforward , like its density , is an intensive property and does not depend on how much of the substance is present. In thermodynamics , the activity of pure solid us 1. Thus yhe concentration terms for A,B and C are unity. So,Kc = DdSimilarly , the activity of a pure liquid is also 1. Thus if a reactant or a product is a liquid, we cant omit in the equilibrium constant expressions.Also we can express the equilibrium constant asKp = P(D)d .Factor Affecting Equilibrium-Chemical equilibrium represents a balance between forward and reverse reactions. In most cases, this balance is quit delicate. alteration in experimental condition may disturb the balance and shift the equilibrium countersink so that variable can be controlled experimentally are concentration, pressure, volume and temperature.Effect of change of temperature- A change in concentration, pressure, or volume may alter the equilibrium position , that is, the relative amounts of reactants and products but it point not change the value of equilibrium constant .Only a change in temperature can alter the equilibrium constant. At equilibrium at a certain temperature, the heat effect is zero because there is no net reaction .If we treat heat as though it were a chemical reagent, than a rise in temperature adds heat to the organization and a drop in a temperature removes heat from the system .As with a change in any another(prenominal) parameter ,(concentration, pressure, or volume), the system shift to reduce the effect of the cha nge. Therefore, a temperature increase favours the endothermic direction (from left to right of the equilibrium equation ) and a temperature decrease favours the exothermic direction.In summary, a temperature increase favours an exothermic direction and a temperature decrease favours the exothermic reaction. The effect of changing temperature on an equilibrium constant is given by the van t Hoff equationd ln K/ d T = H/RT2Thus, for exothermic reactions, (H is negative) K decreases with an increase in temperature, but, for endothermic reactions, (H is positive) K increases with an increase temperature. An alternative formulation isd ln K/ d(1/T) = H/RAt first sight this appears to offer a means of obtaining the standard molar enthalpy of the reaction by studying the variation of K with temperature.Effect of change of pressure and volume- Change in pressure ordinarily do not effect the concentration of the reacting species in condensed phases(say, in an aqueous solution) because liqu ids and solids are virtually in compressible. On the other hand, concentration of gases are greatly affected by change in pressure. The greater the pressure, the smaller the volume, and vice versa. Note, too, that the term (n/V) is the concentration of the gas in mol/L, and it varies directly with pressure.In general an increase in pressure (decrease in volume) favours the net reaction that decreases the total numbers of moles of gases (the reverse reaction, in this case), and a decrease in pressure (increase in volume) favours the net reaction that increases the total numbers of moles of gases(here the forward reaction).For reaction in which there is no change in the numbers of moles of gases, a pressure (or volume)change has no effect on the position of equilibrium.Effect of catalyst at equilibrium -Catalyst does not affect the the equilibrium constant. And it can not shift the equilibrium positon. Catalyst only enhance the rate of reaction to reach the equilibrium position.Effect of concentration of reactant- Effect of concentration change the position of equilibrium. If we increase the concentration of the products shifts the equilibrium to left, and decreasing the concentration of the product shifts the equilibrium to right. These results are just predicted by Le Chatelier principle.Le chatelier principle- If an external latent hostility is applied to a system at equilibrium, the system adjusts in such a way that the stress is partially off set as the system reaches a new equilibrium position.pH -A MEASURE OF ACIDITY.Because the concentrations of H+ and OH- in aqueous solution are frequently very small numbers and thence inconvenient to work with, Soren Sorensen in 1909 proposed a more practical measure called pH.The pH of a solution is defined as the negative logarithm of hydrogen ion concentration in (mol/L)pH = -log H3O+ or pH = -log H+The negative logarithm gives us a positive number for Ph, which otherwise would be negative receivable to small val ue of H+. Furthermore the term H+ permits only to the numerical part of the expression for hydrogen ion concentration, for we cant take the logarithm of units. Thus, like the equilibrium constant, the pH of a solution is a dimensionless quantity.Acidic solutions pH is less than 7.00.Basic solutions pH is more than 7.00.Neutral solutions pH is equal to 7.00.Notice that pH increases as H+ decreases.For real solutions, activity usually differs from concentrations, sometimes appreciably. Knowing the solute concentration, there are reliable ways based on thermodynamics for estimating its activity, but the details are beyond the scope of text.Keep in mind, therefore, that the measured pH of a solution is usually mot same as that , because the concentration of the H+ ion in molar concentration is not numerically equal to its activity value. Although we will continue to use concentration in our discussion, it is important to know that this approach will give us only an approximationOf the chemical process that actually take place in solution phase. In the laboratory, pH of a solution is measured with a pH meter.List of some pH of a number of common fluid, the pH of a body fluid varies greatly, depending on location and function. The low pH (high acidity) of gastric juices facilitates digestion whereas a higher pH of blood is necessary for transport of oxygen.APPLICATION OF pH-A pH indicator is substances that change colour virtually a particular pH. It is weak acid or weak base and the colour changes occur around 1pH unit either side of its acid dissociatian constant.For.ex. Naturaly occuring indicator litmus is red in acid solution and blue in alkaline solution.REFRENCES-P.W. Atkins, Physical Chemistry, third edition, Oxford University Press, 1985.F.van Zeggeren and S.N Steery,the computation of chemical equilibrium,1920.W.R.Smith and R.W.Mission,chemical equilibrium Analysis.RAYMOND CHANG, Williams college.