Sunday, September 29, 2013

Issue 38: Chemistry: Electrochemistry and Organic (Hoyle's Freshman Honor Chem Class)





Oxidation-Reduction reactions involve a transfer of electrons from the substance oxidized to the substance reduced
    ***LEO the lion says GER: loss of electrons is oxidation; gain of electrons is reduction


a.       Rules for oxidation states:
                i.      The oxidation state of an atom in an element is always 0
                ii.      Oxidation state of a monoatomic atom is its charge
                iii.      In compounds, fluorine is -1
                iv.      Oxidation is always -2, except when it is combined with fluorine or in a peroxide
                 v.      The oxidation state of Hydrogen is +1
b.      Electron shift method
                   i.      Divides reaction into two half reactions. These reactions are balanced by using the oxidation number, since charge is conserved.
                   ii.      Multiply if electrons gained and reduced are different
                   iii.      Finally the two equations are added together
c.       Ion electron method


Electro Chem:


ElectroChemistry much like its name implies is about electricity in chemistry, duh...


More specifically electrochemistry, at least what we are learning about deals with cells.


We’re not talking about the cells you find in the body. More like electric cells if you couldn’t figure it out by yourself.


Quoted from the orange book “ an electrochemical cell involves a chemical reaction and a flow of electrons.


There are two types of cells we want to talk about:
Voltaic
Electrolytic


Voltaic Cell:
This is a pretty cool cell, and it also explains how a normal battery works. When I was a child I thought that there was just a bunch of electricity in a battery, however, that seems to not be the case.


Since I don’t like paraphrasing here is another quote: “A voltaic cell is an electrochemical cell in which a spontaneous chemical reaction produces a flow of electrons.”


From this we know that we need a reaction that is spontaneous that can also involve the transfer of electrons. That means we have to use an ionic bond of some sort for the equation. In addition for this transfer of electrons to happen we need an oxidation/ reduction reaction to happen.


Since now we know a few parts that are involved in this cell, I am going to show a diagram.



The overall reaction for this cell is Zn + CuSO4 -> Cu + ZnSo4. The reason why Zn can do this is because it is much more active than Cu, therefore it can replace Cu in the equation
We can ignore the SO4 in this equation because that is a bystander particle, and no one likes those. So the equation becomes Zn+ Cu= Cu+Zn. Now this doesnt make much sense unless you put oxidation numbers on the elements. Now look: Zn(0) + Cu(2+) = Cu(0)+ Zn(2+). From this we can clearly see that Zn is being oxidized, while Cu is being reduced in this equation.


Now lets apply the diagram to this equation. We know that Zn is being oxidized so we can label it as the anode (where oxidation occurs). Also because we know Cu is being reduced we can label that side as the cathode (where reduction occurs).
Oxidation is happening in the anode so electrons are being lost and and transferred through the wire. If the circuit is closed (it isn't in the picture) then the electrons go through the load and get transferred to the cathode. Since electrons are being added to Cu t it is being reduced.


The anode is the negative side which gives away electrons, and the cathode is the positive side that gains electrons, much like the sides in a battery.


If you don’t understand what I am saying, don’t ask me for help, go read the orange book.


Electrolytic cell:


An electrolytic cell requires an electric current (a battery) to force a non- spontaneous reaction to occur.  Previously we have seen Zinc oxidize and give electrons to Cu, however, can the opposite take place? WELL YES!!! You just need a power source because the reaction isn’t spontaneous.


Before I go on I am going to clarify a term:
electrolysis: the process of using electricity to force a chemical reaction.


One purpose of the electrolytic cell is to obtain active elements (ones that are hard to find in nature because they always bond) by the electrolysis of fused salts. So using a electrolytic cell I would be able to separate molten NaCl to obtain the two highly active elements in their pure forms.


Another purpose is to electroplate metals onto a surface. For example I could coat Zn with Copper if I really wanted to.


Ok let us look at a electroplating example:




Ignore the guy on the right.


Ok, from this diagram we can see an anode of Ag silver. The anode is oxidizing creating Ag+ ions while transmitting electrons to the positive side of the battery. The anode metal piece has a positive charge due to oxidation. The electrons that were intercepted by the battery now flow out the negative side of the battery and are forced into the cathode. The cathode now has more electrons and develops a negative charge. Since the anode has a positive charge and the cathode has a negative charge, the Ag+ ions formed by the  anode are attracted to the cathode, therefore plating it with Ag.



Now that we are done with the explanations, I am now going to state the differences and similarities between the two types of cells


Similarities:


Both use redox reactions
The anode is the site of oxidation and the cathode is the site of reduction
Electrons flow through the wire from the anode to the cathode.


Differences:


Voltaic has a spontaneous chemical reaction, while the electrolytic cell is non-spontaneous.
A voltaic cell has a negative anode and a positive cathode, while in an electrolytic cell it is opposite.




Organic Chemistry:


Naming alcohol
- prefix = # of carbons
- # in the front shows the position of where the OH is
- ends in -ol
- an indicates single carbon bond; en indicates double;


E.g. 2-pentanol
5 carbons in the straight chain, all single bonds, OH is in the 2nd position


Naming Ethers:
- Put branches in order of increasing # of carbons.
- Name branches on each side of the Oxygen according to # of C.
- Add ether at the end of the name.
- Add -yl to the end of each branch name


E.g ethyl- propyl ether
2 carbons on one side of the oxygen and 3 carbons on the other side, all singly bonded.


Naming Organic Acids:
- Name ends with Acid
- prefix represents number of carbons.
- suffix for names is -oic
- an signals single bond and en signals a double bonded carbon.


E.g heptanoic acid
7 carbons singly bonded with a double bonded O and single bonded OH on the last carbon.


Naming Ketones:
- # represents the position of the double bonded Oxygen.
- Prefix for # of C.
- ends in -one.


Naming Aldehydes:
- Change the ending of parent chain to -al.



Naming Esters:
- Name the branch according to the # of carbons that does not contain the double bonded O.
- Name the main branch according to the # of carbons that contain the double bonded O.
- Branch goes first in name.
- Ends with -oate





good job =) =.=

Issue 37:Chemistry :Equilibrium (Hoyle's Freshman Honor Chem Class)

Chemistry Equilibrium Test
I.            Physical Equilibrium and Chemical Equilibrium (Physical refers to physical changes in reactions and chemical refers to chemical changes in reactions)
- Dynamic Equilibrium- when the rates of the forward and reverse reactions are equal. The system is dynamic because individual molecules react continuously
- Physical Equilibrium- very similar to chemical equilibrium, physical equilibrium does not involve any change in chemical properties.


- Chemical Equilibrium (Did not learn yet)- the state in which the chemical activities or concentrations of the reactants and products have no net change over time
-  Reversible reactions can proceed in forward and reverse directions and don’t go to completion
- Reverse reaction is faster than forward reaction
-  If concentration of products increase, the forward reaction is faster.
- If concentration of products decrease, the reverse reaction is faster
- At equilibrium, the concentrations of reactants and products are equivalent at constant.
- The concentrations of the reactants does not have to be the same as concentration of products.
II.            Keq=CcDdAaBb when  aA + bB  cC + dD


III.      Ksp=[A-]a[B+]when  AaB  aA + B
- Characteristics of Reversible Reactions:
    • Products can react and form initial reactants
    • Can never go to completion
    • Natural processes. Spontaneous rxn
- Characteristics of Irreversible Reactions:
    • Products cannot react and form initial reactants
    • Can go to completion
    • Does not occur on their own. Non-spontaneous rxn
- Rate of rxn= Change in concentration/ Time taken
- Rate of rxn is directly proportional to concentration of reactants
- Rate of forward reactions decreases as reactions progresses and rate of reverse reactions increases as reactions progresses.
- R of forward rxn= R of reverse rxn
- At equilibrium, K of forward rxn [A][B]= K of [C][C]
- Rxn doesn’t stop at equilibrium
- There is no change in concentration of reactants and products after equilibrium changed
- The value of the equilibrium constant or K depends only on temp. It changes when t changes.
- Rate of melting= Rate of freezing
- Rate of evaporation= Rate of condensation
- Rate of dissolving= Rate of crystallization
- [  ] is molar concentration= Molarity= moles/L
- Factors affecting Rate of rxn:
    • Ionic substance react faster
    • As energy increases, the number of collisions increases.
    • As temp increases, there are more molecules required as there is more enrgy effective and collisions increases, faster rxn
    • Pressure increases, more reactions
    • Catalyst  increases the rate by lowering the energy of activation.


IV.            Collision Theory
·         It states that reactions must have effective collisions with enough energy and proper orientation to react
V.            Factors Affecting Rate of Reaction
·         More exposure and surface area b/w reactants- more collisions
·         Less space b/w molecules, more collisions
·         Increased concentration, more collisions
·         More average kinetic energy or temperature, then more collisions
·         Catalyst causes proper orientation
-    Pressure and temperature (only affects gas)
VI.            Le Chatelier’s Principle
- If a system is at equilibrium and a stress is added or removed to the system, the equilibrium will shift to remove that stress.
  IE: If a stress is added to the left, then equilibrium will shift to the right to balance out
- If concentration increases on left, shift goes to right
- For pressure, equilibrium balances by shifting to the side with the least moles. If both sides have the same number of moles, then changing pressure would have no effect.
- Concentration of reactants will decrease b/c they are used.
- Concentration of products will increase b/c they are formed
- Pressure doesn’t change concentration and effects only gases.
- Pressure increases when equilibrium shifts to the direction of less moles.
- If the reaction is exothermic, then the shift will be to the left. (Exothermic energy released --> warm) and prefer low temp
-  If it is endothermic, the shift will be to the right.(Endothermic energy absorbed -->cold) and prefer high temp.
- Endothermic rxn rate increases by increase in temperature
- When temperature increases, the side with heat experienced more stress. Right side stress, left side shift
- Catalyst speeds up forward and reverse rxn equally and equilibrium reached faster.
- Common ion effect-a common ion from a different compound can shift the equilibrium
- In a thermochemical equation, the side that says heat is the side that experiences stress
VII. Colligative Properties
-Colligative properties-property of solvent that changes when solute is added to solution
-depends on number of particles
- Boiling point elevation and freezing point depression
- Molality= moles of solute/ Kg of solvent
Chemistry: Equilibrium
· Dynamic Equilibrium- when the rates of the forward and reverse reactions are equal. The system is dynamic because individual molecules react continuously
· Physical Equilibrium- very similar to chemical equilibrium, physical equilibrium does not involve any change in chemical properties.
· Chemical Equilibrium- the state in which the chemical activities or concentrations of the reactants and products have no net change over time
Reversible Processes
-          Phase Changes Ex. H2O (l) à H2O (g)
-          Solution Formation Ex. NaCl (s) à NaCl (aq)
-          Reversible Reactions Ex. N2 (g) + 3H2 (g) ó 2NH3 (g)
A system comes to equilibrium when…
-          The rates of the forward and reverse processes are equal
-          The concentrations of the reactants and products are constant
The Law of Mass Action  of aA + bB ó cC + dD
-          Keq = [C]c[D]d / [A]a[B]b
-          NOTE: only gases or aqueous species are included in the equilibrium constant (Keq)
-          Keq changes with TEMPERATURE ONLY
The Equilibrium Quotient (Q)
-          - [C]c[D]d / [A]a[B]b at ANY concentration
Le Chatelier’s Principle: If a system at equilibrium experiences a change in concentration, temperature, or pressure, the equilibrium position will shift to offset the change
RICE Charts
-          R: Reaction
-          I: Initial Concentration
-          C: Change (negative on reactant side, positive on products side)
-          E: Equilibrium
[Example] H2 (g) + I2 (g) ó 2HI (g), Keq = 64. Initial concentration: 0.2 M of H2 and I2, no HI
Ø  R: H2 (g) + I2 (g) ó 2HI (g)
Ø  I:  0.2 M     0.2 M        0
Ø  C:  – x           – x         + 2x
Ø  E: (0.2 – x) (0.2 – x) (2x)
To solve for x:
            Keq = [HI]2 / [H2][I2]
            64 = (2x)2 / (0.2 – x)2
            0.16 = x
Solubility Rules to Know
-          All Group I cations are soluble
-          All nitrates are soluble
-          Halides with Ag. Pb, Hg2 are insoluble
-          Common Ion: solubility is much less in the presence of a common ion
-          Molar Solubility: concentration of ions in a saturated solution of a very insoluble compound
Ion Product (Q) and Solubility Product (Ksp)
-          For AgCl (s) ó Ag+ (aq) + Cl- (aq) à [Ag+] [Cl-]
If…
-          Q > Keq : too much products, the reaction will run in reverse
-          Q < Keq : too much reactants, the reaction will run forward
-          Q = Keq : AT EQUILIBRIUM
-          K << 1 : reactants are favored
-          K >> 1 : products are favored
-          Reactant is added: shifts away fromP the added reactant (right)
-          Product is removed: towards the removed reactant (right)
-          Heat is added: away from the added heat
-          Volume is decreased: pressure increases; shifts towards fewer moles of gases
-          Q > Ksp : it will precipitate
-          Q < Ksp : it will dissolve (unsaturated)
-          Q = Ksp : at equilibrium (saturated)
-          Ksp < 1 : very insoluble species

-          Ksp > 1 : very soluble species