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STPM Chemistry Form 6 Definition List:

   1. The Hund Rule ± orbital with the same energy level (degenerate orbitals), electron will
      occupy different orbital singly/one electron first with the parallel spin, before
      pairing.(Reject: same spin, spin with same direction) STPM 2008, 2007
   2. Pauli Exclusive Principle ± Each orbital can hold a maximum of two electrons with
      opposite spin. (Reject: different spin) STPM 2007
   3. Aufbau principle ± Electrons occupy orbitals with the lowest energy level first. (Reject:
      occupy lower energy first) STPM 2006, 2007
   4. Vapour pressure ± the pressure exerted by a vapour that is in equilibrium with its liquid
      at a fixed temperature in a closed system. It is due to the collision of the vapour particles
      on the walls of the container. STPM 2004

STOICHIOMETRY

   1. Molarity (M) [concentration of a fluid solution] ± defined as the moles of a solute per
      volume of solution.
   2. Density [concentration of a fluid solution] ± defined as the mass of solution per volume
      of solution.
   3. Dilution ± addition of solvent to a solution resulting in an increase in the volume of the
      solution and a decrease in the concentration of the solute in solution.
   4. Precipitation reaction (also refer to as double-displacement reaction) ± a reaction that
      involve two aqueous salts being added together to form ions and a solid salt precipitate.

ACID-BASE EQUILIBRIA

   1.  Arrhenius acid ± acid yields H3O+ when added to water
   2.  Arrhenius base ± base yields OH- when added to water
   3.  Bronsted-Lowry acid (proton donor) ± a substance that donate a proton, H+ to a base.
   4.  Bronsted-Lowry base (proton acceptor) ± a substance that accept a proton, H+ from an
       acid.
   5. Conjugate acid ± a species (molecule or ion) formed when a proton is added to a base.
   6. Conjugate base ± a species (molecule or ion) formed when a proton is removed from an
       acid.
   7. Lewis acid ± an electron-pair acceptor.
   8. Lewis base ± an electron-pair donor.
   9. Electrolyte (also electrolytic conductor) ± a chemical compound that will conduct
       electricity in the molten state or in aqueous solution.
   10. Strong acid ± an acid that is almost completely dissociated in aqueous solution.
       (Stronger the acid, the weaker its conjugate base)
   11. Weak acid ± an acid that is only partially dissociated in aqueous solution. (Weaker the
       acid, the stronger its conjugate base)
STPM Chemistry Form 6 Definition List ± Part 2:

Acid-Base Equilibria

Term                Definition                         Example
Arrhenius acid      Yields H3O+ when added to          aq: [H3O+] > [OH-]
                    H2O
Arrhenius base      Yields OH- when added to           aq: [OH-] > [H3O+]
                    H2O
Bronsted-Lowry acid Proton donor                       HX in protic solvent
Bronsted-Lowry base Proton acceptor                    KOH in protic solvent
Lewis acid          Electron pair acceptor             BF3 in aprotic solvent
Lewis base          Electron pair donor                NH3 in aprotic solvent

Four important concepts (just the berry essence):

   1. Acid dissociation ± (expressed quantitatively) acid dissociation constant, Ka, is nothing
      more than the equilibrium constant for the dissociation reaction of an acid in water.
      Relative strength of an acid (increases), its Ka (increases) and its pKa (decreases).
      (The Ka and pKa of an acid depend on the strength of an acid, but not its concentration.)
   2. Base hydrolysis ± base hydrolysis constant, Kb, nothing more than the equilibrium
      constant for the hydrolysis reaction of a base in water.
      Relative strength of a base (increases), its Kb (increases) and its pKb (decreases).
      (The Kb and pKb of an acid depend on the strength of an acid, but not its concentration.)
   3. Overall Relationship : Acid strength , Ka , pKa , conjugate base strength , Kb , pKb

   4. Strength of a reagent (Ka / pKa and Kb / pKb) ± the completeness of a reaction in water.
      (dissociation = ionisation or electrolytic nature)
      The stronger the acid, the more electrolytic it is, because it conducts electricity better due
      to the greater number of ions in solution.
      The stronger the base, the more readily it undergoes hydrolysis when mixed with water



Acid                        Name                          pKa
Cl3CCOOH                    Trichloroacetic acid          0.64
Cl2HCCOOH                   Dichloroacetic acid           1.27
H2SO3                       Sulfurous acid                1.82
HClO2                       Chloroacetic acid             1.90
ClH2CCOOH                   Chloroacetic acid             2.82
HF                          Hydrofluoric acid             3.15
HNO2                        Nitrous acid                  3.41
HCOOH                       Formic acid                   3.74
H3CCOOH                     Acetic acid                   4.74
2,4-(H3C)2C6H3NH3+   2,4-dimethylanilinium   5.08
4-H2NC6H4NH3+        4-aminoanilinium        6.18
H3CO3                Carbonic acid           6.36
4-O2NC6H4OH          4-nitrophenol           7.15
HClO                 Hypochlorous acid       7.46
HBrO                 Hypobromous acid        8.72
NH4+                 Ammonium                9.26
HCN                  Hydrogen cyanide        9.36
HIO                  Hypoiodous acid         10.66

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57996218-STPM-Chemistry-Form-6

  • 1. STPM Chemistry Form 6 Definition List: 1. The Hund Rule ± orbital with the same energy level (degenerate orbitals), electron will occupy different orbital singly/one electron first with the parallel spin, before pairing.(Reject: same spin, spin with same direction) STPM 2008, 2007 2. Pauli Exclusive Principle ± Each orbital can hold a maximum of two electrons with opposite spin. (Reject: different spin) STPM 2007 3. Aufbau principle ± Electrons occupy orbitals with the lowest energy level first. (Reject: occupy lower energy first) STPM 2006, 2007 4. Vapour pressure ± the pressure exerted by a vapour that is in equilibrium with its liquid at a fixed temperature in a closed system. It is due to the collision of the vapour particles on the walls of the container. STPM 2004 STOICHIOMETRY 1. Molarity (M) [concentration of a fluid solution] ± defined as the moles of a solute per volume of solution. 2. Density [concentration of a fluid solution] ± defined as the mass of solution per volume of solution. 3. Dilution ± addition of solvent to a solution resulting in an increase in the volume of the solution and a decrease in the concentration of the solute in solution. 4. Precipitation reaction (also refer to as double-displacement reaction) ± a reaction that involve two aqueous salts being added together to form ions and a solid salt precipitate. ACID-BASE EQUILIBRIA 1. Arrhenius acid ± acid yields H3O+ when added to water 2. Arrhenius base ± base yields OH- when added to water 3. Bronsted-Lowry acid (proton donor) ± a substance that donate a proton, H+ to a base. 4. Bronsted-Lowry base (proton acceptor) ± a substance that accept a proton, H+ from an acid. 5. Conjugate acid ± a species (molecule or ion) formed when a proton is added to a base. 6. Conjugate base ± a species (molecule or ion) formed when a proton is removed from an acid. 7. Lewis acid ± an electron-pair acceptor. 8. Lewis base ± an electron-pair donor. 9. Electrolyte (also electrolytic conductor) ± a chemical compound that will conduct electricity in the molten state or in aqueous solution. 10. Strong acid ± an acid that is almost completely dissociated in aqueous solution. (Stronger the acid, the weaker its conjugate base) 11. Weak acid ± an acid that is only partially dissociated in aqueous solution. (Weaker the acid, the stronger its conjugate base)
  • 2. STPM Chemistry Form 6 Definition List ± Part 2: Acid-Base Equilibria Term Definition Example Arrhenius acid Yields H3O+ when added to aq: [H3O+] > [OH-] H2O Arrhenius base Yields OH- when added to aq: [OH-] > [H3O+] H2O Bronsted-Lowry acid Proton donor HX in protic solvent Bronsted-Lowry base Proton acceptor KOH in protic solvent Lewis acid Electron pair acceptor BF3 in aprotic solvent Lewis base Electron pair donor NH3 in aprotic solvent Four important concepts (just the berry essence): 1. Acid dissociation ± (expressed quantitatively) acid dissociation constant, Ka, is nothing more than the equilibrium constant for the dissociation reaction of an acid in water. Relative strength of an acid (increases), its Ka (increases) and its pKa (decreases). (The Ka and pKa of an acid depend on the strength of an acid, but not its concentration.) 2. Base hydrolysis ± base hydrolysis constant, Kb, nothing more than the equilibrium constant for the hydrolysis reaction of a base in water. Relative strength of a base (increases), its Kb (increases) and its pKb (decreases). (The Kb and pKb of an acid depend on the strength of an acid, but not its concentration.) 3. Overall Relationship : Acid strength , Ka , pKa , conjugate base strength , Kb , pKb 4. Strength of a reagent (Ka / pKa and Kb / pKb) ± the completeness of a reaction in water. (dissociation = ionisation or electrolytic nature) The stronger the acid, the more electrolytic it is, because it conducts electricity better due to the greater number of ions in solution. The stronger the base, the more readily it undergoes hydrolysis when mixed with water Acid Name pKa Cl3CCOOH Trichloroacetic acid 0.64 Cl2HCCOOH Dichloroacetic acid 1.27 H2SO3 Sulfurous acid 1.82 HClO2 Chloroacetic acid 1.90 ClH2CCOOH Chloroacetic acid 2.82 HF Hydrofluoric acid 3.15 HNO2 Nitrous acid 3.41 HCOOH Formic acid 3.74 H3CCOOH Acetic acid 4.74
  • 3. 2,4-(H3C)2C6H3NH3+ 2,4-dimethylanilinium 5.08 4-H2NC6H4NH3+ 4-aminoanilinium 6.18 H3CO3 Carbonic acid 6.36 4-O2NC6H4OH 4-nitrophenol 7.15 HClO Hypochlorous acid 7.46 HBrO Hypobromous acid 8.72 NH4+ Ammonium 9.26 HCN Hydrogen cyanide 9.36 HIO Hypoiodous acid 10.66