Factors Affecting Solubility

thither ar three main factors that control solvability of a solute. (1) Temperature (2) Nature of solute or response (3) Pressure EFFECT OF TEMPERATURE Generally in many subjects solubility increases with the rise in temperature and decreases with the fall of temperature but it is not necessary in all cases. However we must follow two behaviours In endothermic process, solubility increases with the increase in temperature and vice versa. For example solubility of potassium nitrate increases with the increase in temperature. In exothermic process, solubility decrease with the increase in temperature.For example solubility of calcium oxide decreases with the increase in temperature. Gases are more(prenominal) soluble in cold solvent than in hot solvent. NATURE OF SOLUTE AND SOLVENT Solubility of a solute in a solvent purely depends on the nature of both solute and solvent. A polar solute dissolved in polar solvent. Solubility of a non-polar solute in a solvent is large. A polar s olute has low solubility or insoluble in a non-polar solvent. EFFECT OF PRESSURE The effect of extort is observed only in the case of gases. An increase in cart increases of solubility of a gas in a liquid.For example carbon dioxide is filled in cold drink bottles (such as coca cola, Pepsi 7up etc. ) under mechanical press. Properties of Solution Concentration The density of a root is the measure of how much solute and solvent there is. A effect is voiceless if it contains a large mensuration of solute, or dilute if contains a modest amount. yard Molarity is the number of moles of solute per litre of source. It is abbreviated with the symbol M, and is roundtimes utilise as a unit of measurement, e. g. a 0. 3 molar solution of HCl. In that example, there would be 3 moles of HCl for any 10 litres of water system (or whatsoever the solvent as). Molality Molality is the number of moles of solute per kilogram of solvent. It is abbreviated with the symbol m (lowercase), and is almosttimes utilise as a unit of measurement, e. g. a 0. 3 molal solution of HBr. In that example, there would be 3 moles of HBr for every 10 kilograms of water (or whatever the solvent was). Mole Fraction The mole disunite is simply the moles of solute per moles of solution. As an example, you dissolve wizard mole of NaCl into three moles of water. Remember that the NaCl entrust dissociate into its ions, so there are now five moles of particles one mole Na+, one mole Cl-, and three moles water.The mole figure of sodium is 0. 2, the mole fraction of chloride is 0. 2, and the mole fraction of water is 0. 6. The mole fraction is symbolized with the Greek letter (chi), which is often written simply as an X. Dilution Dilution is adding solvent to a solution to obtain a less concentrated solution. Perhaps you get used dilution when running a lemonade stand. To cut costs, you could take a half-full jug of rich, concentrated lemonade and fill it up with water. The resulting solut ion would take the same total amount of sugar and lemon juice, but simulacrum the total wad. Its flavour would be weaker due to the added water.The key concept is that the amount of solute is constant before and after the dilution process. The concentration is decreased (and volume increased) only by adding solvent. Thus, the number of moles of solute before and after dilution are equal. moles1 = moles2 By definition of molarity, you can find the moles of solvent. M x V = moles Substituting the second equation into the first gives the dilution equation. M1 x V1 = M2 x V2 To adjust the amount of solvent (usually water) that must be added, you must see the initial volume and concentration, and the desired concentration.Solving for V2 in the above equation will give you the total volume of the diluted solution. Subtracting the initial volume from the total volume will determine the amount of pure solvent that must be added. Ionic Solutes When ionic compounds dissolve in water, the y separate into ions. This process is called dissociation. Note that be acquire of dissociation, there are more moles of particles in the solution containing ions than there would be with the solute and solvent separated. If you soak up two glasses of water, and you dissolve salt into one and sugar into the other, there will be a big difference in concentration.The salt will dissociate into its ions, but sugar (a molecule) will not dissociate. If the salt were NaCl, the concentration would be double that of the sugar. If the salt were MgCl2, the concentration would be triple (there are three ions). Solubility Rules Not all ionic compounds are soluble. Some ionic compounds have so much attractive force between their anions and cations that they will not dissociate. These substances are insoluble and will not dissolve. Instead, they clump together as a unfaltering in the bottom of solution. Many ionic compounds, however, will dissociate in water and dissolve.In these cases, the attr active force between ion and water is greater than that between cation and anion. There are several rules to help you determine which compounds will dissolve and which will not. Solubility Rules 1. All compounds with Group 1 ions or ammonium ions are soluble. 2. Nitrates, acetates, and chlorates are soluble. 3. Compounds containing a halogen are soluble, except those with fluorine, silver, or mercury. If they have lead, they are soluble only in hot water. 4. Sulfates are soluble, except when combined with silver, lead, calcium, barium, or strontium. . Carbonates, sulfides, oxides, silicates, and phosphates are insoluble, except for rule 1. 6. Hydroxides are insoluble except when combined with calcium, barium, strontium, or rule 1. Sometimes, when two different ionic compounds are dissolved, they react, resileing a precipitate that is insoluble. Predicting these reactions requires acquaintance of the activity series and solubility rules. These reactions can be written with all ions , or without the spectator ions (the ion that dont react, introduce on both sides of the reaction), a format cognise as the net ionic equation.For example, silver nitrate is soluble, but silver chloride is not soluble (see the above rules). Mixing silver nitrate into sodium chloride would cause a cloudy white precipitate to form. This happens because of a double replacement reaction. Electrolytes When solutes dissociate (or if a molecule ionizes), the solution can conduct electricity. Compounds that readily form ions, thus being good conductors, are known as strong electrolytes. If only a small amount of ions are formed, electricity is poorly conducted, content the compound is a weak electrolyte.A strong electrolyte will dissolve completely. All ions dissociate. A weak electrolyte, on the other hand, will partially dissociate, but some ions will remain bonded together. Colligative Properties Some properties are the same for all solute particles regardless of what kind. These are known as the colligative properties. These properties apply to ideal solutions, so in reality, the properties may not be exactly as calculated. In an ideal solution, there are no forces acting between the solute particles, which is generally not the case. Vapor PressureAll liquids have a tendency for their surface molecules to escape and e drying upate, even if the liquid is not at its boiling sign. This is because the average energy of the molecules is too small for e dehydrationation, but some molecules could gain above average energy and escape. Vapor pressure is the measure of the pressure of the evaporated vapor, and it depends on the temperature of the solution and the quantities of solute. More solute will decrease vapor pressure. The vapor pressure is presumptuousness by Rauolts Law, where X is the mole fraction of the solvent.Notice that the vapor pressure equals that of the pure solvent when there is no solute (X = 1). If X = 0, there would be no vapor pressure at all. This could only happen if there were no solvent, only solute. A solid solute has no vapor pressure. P solution = P pure solvent (X solvent) If two volatile substances (both have vapor pressures) are in solution, Rauolts Law is still used. In this case, Rauolts Law is essentially a linear combination of the vapor pressures of the substances. Two liquids in solution both have vapor pressures, so this equation must be used. P solution = P1 (X1) + P2(X2)The second equation shows the relationship between the solvents. If two liquids were mixed exactly half-and-half, the vapor pressure of the resulting solution would be exactly halfway between the vapor pressures of the two solvents. Another relation in Henrys Law, which shows the relationship between gas and pressure. It is granted by Cg = k Pg , where C is concentration and P is pressure. As the pressure goes up, the concentration of gas in solution must also increase. This is why soda cans release gas when they are opened The decreas e in pressure results in a decrease in concentration of CO2 in the soda. boil Point Elevation A liquid reaches its boiling point when its vapor pressure is equal to the atmosphere around it. Because the presence of solute lowers the vapor pressure, the boiling point is raised. The boiling point increase is given by ?T solution = Kb X m solution The reduced vapor pressure increases the boiling point of the liquid only if the solute itself is non-volatile, meaning it doesnt have a tendency to evaporate. For every mole of non-volatile solute per kilogram of solvent, the boiling point increases by a constant amount, known as the molal boiling-point constant (Kb).Because this is a colligative property, K2 is not affected by the kind of solute. Freezing Point Depression A liquid reaches its frost temperature when its vapor pressure is equal to that of its solid form. Because the presence of the solute lowers the vapor pressure, the freezing point is lowered. The freezing point depression is given by ? T solution = K f X m solute Again, this equation works only for non-volatile solutes. The temperature of the freezing point decreases by a constant amount for every one mole of solute added per kilogram solvent. This constant (K f) is known as the molar freezing-point constant.Osmosis If you studied biology, you would know that osmosis is the movement of water through a membrane. If two solutions of different molarity are placed on opposite sides of a semipermiable membrane, then water will travel through the membrane to the side with higher molarity. This happens because the water molecules are attached to the solvent molecules, so they cannot travel through the membrane. As a result, the water on the side with lower molarity can more easily travel through the membrane than the water on the other side. The pressure of this osmosis is given in the equation. ? = MRTWhere pi is the pressure, M is molarity, R is the gas constant, and T is temperature in Kelvin. Electrolyt es and Colligative Properties When one mole of table salt is added to water, the colligative effects are double those that would have occurred if sugar were added instead. This is because the salt dissociates, forming twice as many particles as sugar would. This dissociation, called the Vant Hoff Factor describes how many particles that are dissociated into the solution and must be multiplied into the Boiling Point Elevation or Vapor Pressure Lowering equations. Different ways of expressing the concentration of solutionsMass Percentage The mass percentage of a component in a given solution is the mass of the component per 100g of the solution. For e. g. , if WA is the mass of the component A, WB is the mass of the component B in a solution. Then, poser A 10% solution of sodium chloride in water (by mass) means that 10g of sodium chloride are award in 100g of the solution. Volume percentage This unit is used in case of a liquid dissolved in another liquid. The volume percentage is defined as the volume of the solute per 100 parts by volume of solution. For e. g. , If VA is the volume of component A present is Vsol volume of the solution.Then, For e. g. , a 10% solution of ethanol C2H5OH, in water (by volume) means that 10cm3 of ethanol is present in 100cm3 of the solution. Strength of a solution is defined as the amount of the solute in gms, present in one litre of the solution. It is expressed as gL-1. Mathematically, Molarity Molarity of a solution is defined as the number of moles of solute dissolved per litre of solution. Mathematically, For e. g. , If a is the weight of the solute (in gms) present in VCC volume of the solution. Then, Molarity is expressed by the symbol M. It can also be expressed as, NormalityNormality of a solution is defined as the number of gram equivalents (gm. e) of a solute dissolved per litre of the given solution. Mathematically it is, For e. g. , If a is the weight of the solute (in gms) present in VCC volume of the solution. Th en, Normality is expressed by the symbol N. It can also be expressed as, relationship between molarity and normality The molarity and normality of a solution is related to each other as follows Molality Molality of a solution is defined as the number of moles of solute dissolved in 1000g of a solvent. Mathematically, it is expressed as Molality is expressed by the symbol m.Molality does not change with temperature. formalness In case of ionic compounds like KCl, CaCO3 etc. Formality is used in place of molarity. It is the number of gram formula masses of solute dissolved per litre of the solution. It is de celebrated by the symbol F. Mathematically it is given as, Mole Fraction It is the ratio of number of moles of one component (solute or solvent) to the total number of moles of all the components (solute and solvent) present in the solution. It is denoted by the symbol X. Let us suppose that a solution contains two components A and B and suppose that nA moles of A and nB moles of B are present in the solution then,Adding eq (i) and (ii) we get XA + XB = 1 Parts per million (ppm) When a solute is present in very small amounts, its concentration is expressed in parts per million. It is defined as the amount of the solute present in one million parts of the solution. It may be noted that the concentration units like molarity, mole fraction etc. are preferred as they train the weight of the solute and solvent, which is independent of the temperature. But units like, molarity, normality etc. , involve volume of the solution, hence changes with temperature.