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reversible reaction
a chemical reaction in which the products re-form the original reactants
Atomic level
No change except structure, rearranged, not created or destroyed
activation energy
the minimum amount of energy required to start a chemical reaction
temperature increase in an exothermic equilibrium will cause the reaction to shift _____
left, favouring the endothermic reaction.
Temperature decrease in an exothermic equilibrium will cause a shift ___.
right, favouring the exothermic reaction.
Temperature increase in an endothermic equilibrium will see a shift ____.
right, favouring the endothermic reaction.
Temperature decrease in an endothermic reaction will see a shift ____.
left, favouring the exothermic reaction.
If pressure is increased in a system, which way will the equilibrium shift to minimise the disruption?
To the side with less molecules present.
If pressure is decreased in a equilibrium, which way will the reaction shift to minimise the disruption?
To the side with more molecules present.
How can you tell if a system is at equilibrium (graph)?
The products/ reactants will have parallel lines to one another and unchanging.
If the concentration of the reactants is increased, how will the system move to minimise the disruption?
Shift to the right - create more products.
If the products from an equilibrium are removed, what will the system do to minimise the disruption?
Shift right. There will be an effort to create more products.
Le Chatelier's Principle
States that if a stress is applied to a system at equilibrium, the system shifts in the direction that relieves the stress.
Kc =
[products]/[reactants]
Kc tells us
Indicates the relationship between product and reactant concentrations at equilibrium.
Kc <1
at equilibrium, the reactants will be favoured
Kc > 1
at equilibrium, the products will be favoured
At equilibrium Kc=
Qc
If Qc is larger than Kc, what way will the equilibrium shift to balance?
left, create more reactants.
If Qc is smaller than Kc, what way will the equilibrium shift to balance?
right, to create more products.
Acids are
proton (H+) donors
Bases are
proton acceptors
monoprotic acid
an acid that can donate only one proton (hydrogen ion) per molecule
diprotic acid
an acid that can donate two protons per molecule
polyprotic acid
an acid that can donate more than one proton per molecule
Ka =
[H+][A-]/[HA]
Kw =
[H+][OH-]
Kb =
[BH+][OH-]/[B]
Ka tells us
The dissociation of acid
pH =
-log[H+]
pOH =
-log[OH-]
Bronsted-Lowry
Common definition of acids as proton donors and bases as proton acceptors.
conjugate base
the particle that remains when an acid has donated a hydrogen ion
conjugate acid
the particle formed when a base gains a hydrogen ion
Amphiprotic
having characteristics of both an acid and a base and capable of reacting as either
buffer solution
a solution made from a weak acid and its conjugate base that neutralizes small amounts of acids or bases added to it
end point of titration
the point at which the indicator changes colour
equivalence point
the point at which the two solutions used in a titration are present in chemically equivalent amounts
half-way equivalence point
pH=pKa
titration curve
a graph of the pH of a solution as a function of the volume of the added titrant
weak acid
an acid that is only slightly ionized in aqueous solution
acid-base indicator
a chemical dye whose colour is affected by acidic and basic solutions
indicators will change colour when:
pH = pKa (choose accordingly)
REDOX reactions include:
displacement reaction of metals, combustion, explosion and electrochemical processes
redox reaction
A chemical reaction involving the transfer of one or more electrons from one reactant to another; also called oxidation-reduction reaction.
The position of an atom on the periodic table can help predict whether it will ____
be oxidised or reduced
reducing agent
The electron donor in a redox reaction, gets oxidised.
oxidisng agent
The electron acceptor in a redox reaction, gets reduced.
Oxidation
loss of electrons
reduction
gain of electrons
How to balance redox reactions in acidic conditions?
find half equations, balance all except H and O, add H+ to even the hydrogen, add H2O to balance the Os, add e- to balance charges, add half equations back together.
Oxidation number of hydrogen in a METAL HYDRIDE (NaH, CaH2)
-1
oxidation state of transition metals can be represented by
roman numerals.
Oxidation number of oxygen in a compound with fluorine
Positive, usually +2, work it out.
Oxidation number of oxygen in peroxides
-1.E.g H2O2, BaO2
Oxidation Numbers of halogens
Always -1 for fluorine and always -1 for others except when bonded to oxygen or another G17 element above them.
Which element should receive the negative oxidation number?
The most electronegative because it attracts electrons more strongly.
galvanic cell
a device in which chemical energy is changed to electrical energy
electrolytic cell
an electrochemical cell used to cause a chemical change through the application of electrical energy
reactions in a galvanic cell are _____
spontaneous
Reactions in an electrochemical cell are _____
non-spontaneous
Why is a salt bridge necessary in a galvanic cell?
Movement of charged ions
Why is an external wire necessary?
Movement of electrons
Standard electrode potential
The voltage measured under standard conditions when a half cell is connected to a standard hydrogen electrode.
oxidising and reducing agents further apart on the reactivity series of metals will have _______
higher electrode potentials
oxidising and reducing agents closer on the reactivity series of metals will have ____
lower electrode potentials
Metal plating can be completed through the use of a ______
electrolytic cell
Alkane
a hydrocarbon containing only single covalent bonds
Alkene
C=C
Alkyne
triple bond
Alcohol
R-OH
Aldehyde
CHO
Ketone
RCOR
carboxylic acid
COOH
Haloalkane
R-X (X=F, Cl, Br, I)
Ester
RCOOR
Nitrile
RCN
Amine
NH2
Amide
RC(=O)NR′R″
Stereoisomers
Compounds with the same structural formula but with a different arrangement of the atoms in space.
Structural Isomers
Compounds with the same molecular formula but different structural arrangements of the atoms within the molecule, resulting in different properties and functions.
geometric isomers
Compounds that have the same molecular formula but differ in the spatial arrangements of their atoms around a double bond. (cis and trans)
Solubility in water
whether or not a substance dissolves in water
Factors that determine solubility in water
1. polar dissolves in polar, nonpolar dissolves in nonpolar (organic)
2. compounds with less than 5 carbons and a polar group are water soluble (exception, sugars are water soluble)
3. charged functional groups are soluble in water
intermolecular forces include
dispersion forces, dipole-dipole forces, hydrogen bonds
What functional groups will form hydrogen bonds?
carboxylic acids, alcohols, amines and amides
Carboxylic acids have high boiling points as they can form...
dimers (increase the dispersion forces)
Carbonyl compounds: BP trends
higher than hydrocarbons (as O present) so dipole-dipole interactions exist
What is the general trend as hydrocarbon chain length increases?
As chain length increases, the boiling point increases. So, harder to break bonds because more energy is required to increased surface area, hence intermolecular forces.
What is the effect of branching on boiling point?
closer molecules can fit together, meaning higher IMF (higher BP)
What is the trend around BP as alcohols go from primary --> tertiary?
Primary = high BP and Tertiary = lower BP
Which would have a higher BP. Diethyl ether or n-butanol?
n-butanol as if exhibits H-bonding
Do amines and amides have stronger IMF than alcohols?
No. N is not as electronegative as O.
As hydrocarbon chain length increases, what happens to the BP?
IMFs increase, hence, there is an increase in BP.
T or F? Even numbered carbon chains will have higher IMFs than odd chains?
True. Even numbered C chains will pack together tighter
Volatility
a measure of how readily a substance vaporises
If a molecule has high IMFs and therefore a high boiling point, would you expect this to be highly volatile?
No. Due to high IMFs it will be hard to break the bonds in the molecule - won't vaporise easily
Haloalkanes are generally what state at room temperature?
liquids
Will a haloalkane have a higher BP than its' hydrocarbon derivative?
yes, due to increases molecular mass and H-bonding.
saturated hydrocarbon
A hydrocarbon in which all the bonds between carbon atoms are single bonds