Advantages And Disadvantages Of Hydrocolubic Solubility

I. LIQUID - Identification of an Unknown Liquid: Using the physical properties of Solubility, Density, and Boiling Point.

increasing the waste of HCl. Water was also used to wash the vial to remove all solids

The principals of stoichiometry and limiting reagents were used to predict that amount of product that is produced when mixing two solutions to produce an insoluble product. We were able to determine this information by starting with a balanced chemical equation: 3CuCl2 2H2O +2Al  3Cu +2AlCl3

6. The solubility of the solids were tested using a micro tray, by placing them in water and oil to observe their polarity,

Substance A and B were weighed; Substance A weighed 0.502 g and substance B weighed 0.503 g. Both substances were put into two different test tube with approximately 8 ml of DI water into the test tub. Substance A and B were stirred and B dissolved while A did not. This shows that B is soluble in water compared to A. Thus, shows that B is soluble in water than A. The reason why B is soluble in water is because it has a higher dipole moment than A. With a higher dipole moment, it shows that it is soluble in water since it is polar and the bonds were easily broken.

AP Chemistry Background The solubility product constant, Ksp, is a particular type of equilibrium constant. The equilibrium is formed when an ionic solid dissolves in water to form a saturated solution. The equilibrium exists between the aqueous ions and the undissolved solid. A saturated solution contains the maximum concentration of ions of the substance that can dissolve at the solutions temperature. A knowledge of the Ksp of a salt is useful, since it allows us to determine the concentration of ions of the compound in a saturated solution. This allows us to control a solution so that precipitation of a compound will not occur, or to find the concentration needed to cause a precipitate to form. The solubility product which will be

2) Explain the trend in the solubility of the three alcohols in water. (In your discussions, bring out the theoretical concepts on which

solvent- able to dissolve other substances, the liquid in which a solute is dissolved to form a solution

By identifying the solubility of the unknown, it could lead to a closer interpretation as to what the functional group the unknown may be. Solubility is determined based on intermolecular attractive forces, such as hydrogen bonding, dipole-dipole, and London dispersion forces. Intermolecular attractive forces arise due to different electron environments in different molecules. For example, water molecules are good at dissolving

The objectives in this laboratory were to be able to observe and discuss solubility while working with several metal ions and reagents. This was done through the use of spot tests to determine if the metal ion and reagent would form a precipitate. If a substance forms, this concluded that a precipitate had formed. This process appears simple, however when several metal ions are combined into one solution a new approach must be taken. It becomes necessary to follow a well detailed, multi step flow chart in order to test for cations and ions (as in table 1.3).

The purpose of using solubility analysis on an unknown is to narrow the possible unknowns given based on the solubility analysis. Acetone was a control for ketone and was soluble in water. Hexanal was a control for an aldehyde and was insoluble in water due to intermolecular forces, such as an increased amount of hydrophobic area rather than hydrophilic area. As a result, by identifying the solubility of the

Continually, the solution was allow to cool down, before it was reheated to dissolve the solid. The solution stood undisturbed until crystals were formed. Solubility tests were performed on all possible solvent-solute pairings. The most efficient pair was

Proposed mode of action for RIS (benzisoxazole derivative) is blocking of 5-HT2A and dopamine D2 receptors. Despite of its potential, RIS is reported to have higher log P value along with poor water solubility and is classified as biopharmaceutical classification system (BCS) class II drug [6]. This poor water solubility leads to limited oral bioavailability through gastrointestinal tract as well as by parenteral route and limits the use of aforementioned drug candidate [4]. Various solubility enhancement techniques can be used to enhance apparent solubility of BCS class II drugs such as salt formation, solid state modification, use of co-solvents, hydro-trophy, complexation with cyclodextrins size reduction etc. Researchers have reported solid dispersion [7], self-nano-emulsifying powder [8] and co-solvent [9] approach for enhancement of RIS water solubility. Use of sodium lauryl sulphate (SLS) in marketed formulation (Risperdal®) of drug presents the probability of solubility enhancement with the use of surfactant [10]. All these approaches have their own advantages and limitations like toxicity issues associated with use of co-solvents [11] (generally water miscible organic solvents) and surfactants beyond a particular level

The absorbance obtained from the results of each test sample, then put into the equation of calibration curve in accordance with the respective raw substances, after which it would have obtained the value of molar absorptivitas. The molar absorptivitas results obtained are used in the determination of the percentage of the sample levels

In this experiment, a system of a sparingly soluble salt in water is studied. From the solubility information