- •1.Molecular orbital of o2
- •2. The first Law of thermodynamics. Enthalpy. Show the calculation of enthalpies of reaction based on Enthalpies of Formation.
- •3. The second Law of Thermodynamics. Entropy. Free Energy and Spontaneity.
- •4. Why electrolytes are classified into strong and weak, give a detail answer. Bronsted and Lowry theory.
- •5. Crystal field theory using as an example of inorganic complex compounds.
- •7. Quantum theory of the hydrogen atom. Quantum numbers, their physical meaning. Heisenberg's uncertainty principle.
- •8. Theory of acid and base. Bronstend and Lowry theory. The pH calculations for acid and base solutions.
- •9. Main principles to fill electronic configuration of atoms. Please show by using specific examples.
- •10. The wave functions ψ, ψ2, and their physical meaning. Schrodinger equation. Application of the method of linear combination of atomic orbitals (lcao).
- •15. Describe spectrochemical series of ligands. The concept of crystal field stabilization energy (cfse) and stability of the complexes
- •16. Factors affecting the chemical equilibrium constant and do not affect it (give examples), its significance in practice. Relationship with the magnitude of the Free Energy.
- •17. Nature of chemical bonding in metals. Electronic band structure.
- •18. Describe influence of temperature on rate of chemical reaction. Give determination of Vant-Hoff’s law and write the Arhenius’s equation.
- •19. Describe hydrolysis of salts as an acid-base interaction. Give a definition of constant and the degree of hydrolysis.
- •20. Describe the Hess's Law, its consequences and their use in the calculation of the thermodynamic processes.
- •21. Characteristics of hydrogen compounds of elements in relation to the distribution of elements in the periodic table.
- •22. Anomalous properties of fluorine and its compounds in the group of halogens (simple hydrogen and oxygen compounds).
- •23. Internal periodicity in lanthanide and actinide families. Radioactivity and its types. The uranium and thorium series, explain why they create series.
- •24. The four types of periodicity of properties change in the periodic table. Secondary and internal periodicities.
- •25. Describe the hydrolytic ability of salts (give examples). Give a definition: The ionic product of water. Autoionization of water.
- •26. General group trends in Binary Acid Strength. Variation of Binary Acid Strength Across Periods. Structure and Relative Strengths of Oxoacids.
- •27. Describe types of isomers of complex compounds. Cis-and trans-isomers. Trans effect ligands.
- •28. Chemistry of Metals. Provide Comparative analysis.
- •29. The characteristic features of the structure and properties of the general laws of d - elements. Give examples.
- •30. General characteristics of VII a group elements.
- •31. General characteristics of VI a group of elements. Trends of major parameters up to down.
- •40. Calculate the concentration of the various ionic species at equilibrium in a 0.1 m solution of h2so4 at 25 c. Ka for hso4- is 1.2x10-2.
5. Crystal field theory using as an example of inorganic complex compounds.
6. Ways of expressing the concentration of solutions.
A solution can be semi-quantitatively described as
unsaturated: a solution in which more solute will dissolve, or
saturated: a solution in which no more solute will dissolve.
The solubility of a solute is the amount of solute that will dissolve in a given amount of solvent to produce a saturated solution. For example, at 0oC, we can dissolve a maximum of 35.7 g of solid NaCl in 100 mL of water (a saturated solution). Any additional solid NaCl that we add to the saturated solution simply falls to the bottom of the container and does not dissolve.
Percent Composition (by mass)
We can consider percent by mass (or weight percent, as it sometimes called) in two ways:
The parts of solute per 100 parts of solution.
The fraction of a solute in a solution multiplied by 100.
We need two pieces of information to calculate the percent by mass of a solute in a solution:
The mass of the solute in the solution.
The mass of the solution.
Use the following equation to calculate percent by mass:
Example:
Molarity
Molarity tells us the number of moles of solute in exactly one liter of a solution. (Note that molarity is spelled with an "r" and is represented by a capital M.)
We need two pieces of information to calculate the molarity of a solute in a solution:
The moles of solute present in the solution.
The volume of solution (in liters) containing the solute.
To calculate molarity we use the equation:
Example:
Molality
Molality, m, tells us the number of moles of solute dissolved in exactly one kilogram of solvent. (Note that molality is spelled with two "l"s and represented by a lower case m.)
We need two pieces of information to calculate the molality of a solute in a solution:
The moles of solute present in the solution.
The mass of solvent (in kilograms) in the solution.
To calculate molality we use the equation:
A 1-molal solution contains one mole of solute per 1 kg of solvent. Molality is a hybrid concentration unit, retaining the convenience of mole measure for the solute, but expressing it in relation to a temperature-independent mass rather than a volume. Molality, like mole fraction, is used in applications dealing with certain physical properties of solutions; we will see some of these in the next lesson.
Example:
Mole Fraction
The mole fraction, X, of a component in a solution is the ratio of the number of moles of that component to the total number of moles of all components in the solution.
To calculate mole fraction, we need to know:
The number of moles of each component present in the solution.
The mole fraction of A, XA, in a solution consisting of A, B, C, ... is calculated using the equation:
To calculate the mole fraction of B, XB, use:
Mole fraction formula/equation: Xsolute = nn+NThe mole fraction of the solvent, then would be: Xsolvent = Nn+N Mole fraction does not have any unit. Sum of the mole fractions of solute and solvent would be unity. Xsolute + Xsolvent = 1
Example:
