Relative masses, charges of subatomic particles
Proton: 1, +1 Neutron: 1, 0 Electron: Negligible, -1
Relative Atomic Mass definition
Average mass of atoms of that element taking into account the mass and amount of each isotope it contains, on a scale where the mass of a C-12 atom is 12
Relative Atomic Mass formula
((mass no.1×%abundance)+(mass no.2×%abundance)+⋯)/100
History of the atom
John Dalton: Atoms could form compounds
JJ Thompson: Before the discovery of the electron, atoms were thought indivisible. The electron led to JJ Thompson's plum pudding model (ball of positive charge with e- embedded in it).
Ernest Rutherford: After the Gold foil experiment (fired alpha particles at thin gold foil), Ernest Rutherford, concluded that the mass of at atom was concentrated at the centre, in a charged nucleus and most of the atom was empty space. If the plum pudding were correct, then all the particles would go straight through, but some bounced back (hit hard, dense nucleus), some veered off (repelled by positive nucleus), and some went through (empty space)
Niels Bohr: Energy levels (the electrons in an atom occupy the lowest available energy levels/shells until given energy)
Further experiments concluded: Positive charge of the nucleus could be divided into protons
James Chadwick: Proved the existence of neutrons within the nucleus.
What would have happened in Rutherford's experiments if the Plum pudding model were correct
All fast, highly charged alpha particles would pass through unhindered. This is because the positive charge and mass in the plum pudding model would be spread out throughout the entire very large volume of the atom, so in a single point that a tiny alpha particle would pass through, the charge would be too low to deflect it.
Plum pudding model vs Nuclear model
Positive charge - spread throughout in PP vs in centre in N
Negative charge - spread throughout ball of positive charge in PP vs electrons orbiting nucleus in N
Neutrons - none in PP vs in nucleus in N
Space - atom is solid with no empty space in PP vs atom mostly empty space in N
Mass - spread evenly throughout in PP vs in centre in N
Atomic mass vs Atomic number
Atomic mass: The sum of protons and neutrons (bottom) Atomic number: a unique number of protons = electrons (if atom) (top)
How is the periodic table arranged?
by increasing atomic number in groups of similar properties (occur at relative intervals - periodicity), and valency in periods of occupied electron shells
Relative atomic mass formula
RAM = (Mass no x abundance) + (Mass no. x abundance) / 100
Ions of metals
positive
Ions of non-metals
negative
Properties and Trends for Noble Gases/Group 0 (Appearance, Reactivity, Compound properties, Boiling/Melting points, density)
Gases
Unreactive due to stable electron configuration
Rarely form compounds
Have full outer shell
The boiling points of the noble gases increase with increasing relative atomic mass (going down the group)
Density increases down the group as atoms have higher RAM
Do not form ions
Properties and Trends for Alkali Metals/Group 1 (Appearance, Reactivity (+water reaction), Compound properties, Boiling/Melting points, density)
Metals
Appearance: dull when exposed to air and shiny
Very easy to cut and easier as you go down
Low densities. Less dense than water for first 3 and density increases down (potassium is an anomaly)
Relatively low melting points, decreasing as the atoms get bigger going down the group
All are very reactive due to valency of 1. The reactivity of the elements increases going down the group because of the increasing distance between the nucleus and the outer electron down the group, which results in a decreased force of attraction so it is lost easier
Reaction with water is more vigorous as you go down. It produces effervescence, an alkali solution (the metal dissolves), hydrogen and it is exothermic
Form white compounds
When reacting with water, forms alkaline solution
(As you go down the group, the metallic force of attraction decreased due to the sea of delocalized electrons being further away from the positive ions, so it easier to cut, and the melting and boiling points decrease. The density increases as you go down the group because there is a higher increase in mass than volume)
Group 1 reaction with oxygen (specifically first 3) and description
4Alkali metal + O₂(g) -> 2[Alkali metal]₂O(s) The metals burn with different colour flames
Group 1 reaction with water (specifically first 3) and description
Alkali metal + H₂0(l) -> [Alkali metal]OH(aq) + 1/2 H₂(g) All react with water to produce hydrogen gas (effervescence) and an alkaline solution containing metal hydroxide (metal dissolves). Exothermic reaction
Group 1 reaction with chlorine (specifically first 3) and description
2Alkali metal + Cl₂(g) -> 2[Alkali metal]Cl(s) All burn in chlorine to form metal chlorides which are white powders
Description of lithium reaction with water
Fizzes, moves on the surface of the water
Description of potassium reaction with water
Fizzes, melts into a ball, burns with lilac flame (hydrogen ignites), moves on the surface of the water
Description of caesium reaction with water
Explosive reaction
Definition of sublimination
When the melting and boiling points come together so liquid state is skipped
Properties and Trends for Halogens/Group 7 (Appearance, Reactivity, Compound properties, Boiling/Melting points, density)
Non-metals
Diatomic (exist in covalently bonded pairs to become stable)
They make halide salts (e.g. Chlorine in Sodium Chloride)
All are very reactive as they need only one electron to become stable and the reactivity decreases down the group because the distance between the outer shell and nucleus increases, so the electron is weakly attracted, and so in a displacement reaction (e.g. in a salt), the halogens would switch places when they come together as the electron is then more strongly attracted to the other nucleus so it moves and the halogen displaces the other
Low melting/boiling points, increase down the group as the atoms get heavier
Halogen appearances - Fluorine, Chlorine, Bromine, Iodine
Fluorine: pale yellow gas Chlorine: pale green gas Bromine: Dark brown liquid w/orange gas Iodine: grey solid (as a gas - 184°C - violet)
Halides meaning
Compounds made from Halogens
Displacement reaction between Chlorine and Potassium iodide
Cl₂ + 2KI -> 2KCl + I₂
Properties and Trends for Transition metals (Appearance, Reactivity, Compound properties, Boiling/Melting points, density, Conductivity)
Found in the D-block (not all elements in the D-block are transition metals
First row is Titanium - Copper
Many can form ions with different charges (e.g. Iron (II) oxide)
Form coloured compounds
Act as catalysts (e.g. copper can speed up Zinc + Sulfuric Acid reaction)
Good thermal and electrical conductors
Shiny when polished (retain it unlike Group 1)
Stronger and Harder
Low reactivity
High density
Boiling/Melting points higher than Group 1
History of the Periodic Table
Before discovering protons, neutrons and electrons, scientists tried to classify the elements by arranging them in order of their atomic weights (i.e. relative atomic mass) The early periodic tables were incomplete and some elements were placed in inappropriate groups if the strict order of atomic weights was followed. Newlands found the 'Law of Octaves' as the properties seemed to repeat every 8th element Mendeleev overcame some of the problems by leaving gaps for elements that he thought had not been discovered and in some places changed the order based on atomic weights. Elements with properties predicted by Mendeleev were discovered and filled the gaps. Knowledge of isotopes made it possible to explain why the order based on atomic weights was not always correct.
Differences between Mendeleev's table and the modern one
No gaps
More elements
Actinide and Lanthanide section
Noble gases
D-block of Transition metals
Mendeleev had some boxes with 2 elements in
Compound definition
Substance made from 2 or more elements chemically bonded together with a fixed proportion Can only be separated by chemical reaction
Mixture definition
More than one substance NOT CHEMICALLY BONDED with any proportions Can be separated through: Filtration, Evaporation, Crystallisation, Distillation, Chromatography
Saturated Solution definition
A solution in which no more solid can dissolve at that temperature
General properties of metals (Melting and boiling points, Conductivity, Appearance, Malleability, Bonding, Acid/base oxides)
High m.p. and b.p. Thermal and electrical conductor Shiny when polished Can be hammered into shape Ionically bonds with non-metals Metallically bonds with metal Metal oxides are basic
General properties of non-metals (Melting and boiling points, Conductivity, Appearance, Malleability, Bonding, Acid/base oxides)
Low Thermal and electrical insulator Dull Brittle as solids Ionically bonds with metals Covalently bonds with non-metals Non-metal oxides are acidic
Method of separation for Insoluble solid and liquid
Filtration - solid: residue, liquid: filtrate
Method of separation for Soluble solid dissolved in a solvent
Evaporation or Crystallisation for solid Simple Distillation for solvent (see image)
Method of separation for Soluble solids dissolved in solvent
Chromatography
Method of separation for Two miscible liquids (liquids that mix)
Fractional Distillation (see image)
Method of separation for Two immiscible liquids (liquids that don't mix)
Separating Funnel
2 types of solvent
Polar solvents (e.g., water) can dissolve ions and polar molecules
Organic solvents (e.g., alcohols, cyclohexane) are useful for non-polar substances
Practical: separating rock salt to get pure NaCl & sand
Add warm water to dissolve the NaCl as it is soluble and stir to ensure fully dissolved
Filter the sand out using filter funnel, paper and flask
Add extra water to ensure all solution has gone through (wash through)
Dry the sand in an oven
Evaporate the water out by heating gently with a Bunsen burner in an evaporating basin. Heat to the point of crystallisation/to the point is starts bubbling to leave water of crystallisation
Leave to allow crystals to form slowly for at least 24 hrs
Pat dry the crystals
Ionic bonding definition
Electrostatic attraction between positive and negative ions
Covalent bonding definition
Electrostatic force of attraction between the nuclei and shared electrons (non-metals only)
Metallic bonding definition
Electrostatic attraction between positive metal ion and delocalised electrons
Structures (4 of them)
Giant Ionic lattice Simple molecular Giant covalent lattice, e.g., diamond, graphite, silicon, silicon dioxide Giant metallic lattice
Giant ionic lattice melting/boiling point
High - lots of energy needed to break lots of ionic bonds
Giant ionic lattice electrical conductivity
solid: non-conductor liquid/aqueous: conductor
Giant covalent lattice melting/boiling point
Very High - lots of energy needed to break lots of covalent bonds
Simple molecular electrical conductivity
Non-conductor (no ions and no delocalised e-)
Simple molecular melting/boiling point
Low - little energy needed to overcome weak intermolecular forces
Giant covalent lattice electrical conductivity
Non-conductor (except graphite)
Giant Metallic lattice melting/boiling point
High - lots of energy needed to break lots of metallic bonds
Giant Metallic lattice electrical conductivity
Conductor (delocalised e-)
Reason for thermosoftening polymers softening
Polymers contain very large molecules with covalent bonds. Thermosoftening polymers soften or melt when heated as the molecules are not joined together (intermolecular forces are strong enough due to large molecules to keep them solid at room temperature)
Reason for alloys' higher strength over pure metals
Pure metals are malleable as the metallic lattice has layers of atoms which can slide over each other Alloys are not as they have other elements of different sizes which distort the layers so they can't slide over each other
Forms (allotropes) of carbon
Graphite Diamond Graphene Fullerenes Carbon nanotubes
Graphite structure
Giant covalent lattice bonded in flat layers (hexagons) which are weakly attracted to each other. Each carbon is bonded to 3 others, leaving a delocalised outer shell e- on each atom free to move along the layers
Graphite melting/boiling point
Very high
Graphite Hardness
Soft (layers slide over with weak intermolecular forces)
Graphite electrical conductivity
✔
Graphite uses + reasons
Electrodes as they are unreactive, cheap, can withstand high temperatures, is a conductor Pencil
Diamond structure
Giant covalent lattice where each carbon is bonded to 4 others in a tetrahedral arrangement
Diamond melting/boiling point
Very high
Diamond hardness
Very hard
Diamond electrical conductivity
✘
Diamond uses
Jewellery Drill bits + saw tips
Graphene melting/boiling point
Very high
Graphene structure
Giant covalent lattice - one layer of graphite (one atom thick) Each carbon is bonded to 3 others, leaving a delocalised outer shell e- on each atom free to move along the layers
Fullerene structure
Simple molecule. Has a spherical shape with hexagonal or pentagonal rings. Hollow at the centre of the molecule. Each carbon is bonded to 3 others, leaving a delocalised outer shell e- on each atom but e- cannot move between molecules
Fullerene electrical conductivity
✘
Fullerene uses
Delivery of drugs (hollow part) Lubricants in metal as it can roll Catalysts
Carbon nanotubes structure
Giant covalent lattice Very high length Tubes of graphene sheets. Each carbon is bonded to 3 others, leaving a delocalised outer shell e- on each atom free to move along the tube
Carbon nanotubes melting/boiling point
Very high
Carbon nanotubes hardness
High tensile strength + very hard
Carbon nanotubes electrical conductivity
✔
Carbon nanotubes uses
Reinforce tennis racquets + golf clubs
Reason for nanoparticles behaving differently to bulk
Behave differently as the increased surface area: volume ratio means that there are more particles on the surface which can react, and they tend to clump together.
Uses of nanoparticles
Fuel cells require platinum as a catalyst so to lower costs, platinum nanoparticles are being used
Delivery of drugs - Gold nanoparticles are used to reduce the amount of the drug needed and reduce side effects of the drug by delivering them to specific cells.
Sun creams - Nanoparticles of Titanium dioxide and Zinc oxide are used to absorb harmful UV radiation and are clear and colourless, and give better skin coverage
Synthetic skin - Nanoparticles (e.g., carbon nanotubes) are being used to create better synthetic skin that is stronger and more flexible (and maybe sense touch and heat)
Cosmetics - In face creams in emulsions that contain vitamins, In moisturisers to kill bacteria, In foundations to diffuse light to partially disguise wrinkles Deodorants - Silver nanoparticles kill bacteria to prevent odour Electronics - Used to make smaller components
Nanoparticles dangers
Nanoparticles may penetrate cell membranes to enter cells and cause DNA damage which can cause mutation and increase risk of cancer
Advantages of dot cross diagram for ionic bonding
Shows the electron structure of the ions
Disadvantages of dot cross diagram for ionic bonding
Can give impression that the structure is only pairs of ions
Advantages of 2D space-filling structure for ionic bonding
Very easy to draw
Disadvantages of 2D space-filling structure for ionic bonding
Can give impression that structure is limited to a few ions
Only shows 2D structure
Advantages of ball and stick structure for ionic bonding
Helps show how the ions are arranged relative to each other
Disadvantages of 3D space-filling structure for ionic bonding
Can give impression that structure is limited to a few ions
Advantages of 3D space-filling structure for ionic bonding
Gives good representation of how the ions are packed together
Disadvantages of ball and stick structure for ionic bonding
May look like covalent bonds
May look that ions are a long way apart
Relative Formula Mass
Sum of the relative atomic masses of all the atoms in the formula - Mr
Avogadro's constant
6.02 × 10²³
Conservation of mass
Total mass of reactants = total mass of products (prove using relative formula masses). NB: any 'missing' mass is the mass of gas (not weighed) which has escaped into the air
Thermal decomposition definition & example with Calcium Carbonate
A reaction where heat causes a substance to break down into simpler substances CaCO₃ → CaO + CO₂
Excess
When the amount of a reactant is greater than the amount that can react (ensures all of the other reactant is used up)
Limiting reactant
The reactant in a reaction that determines the amount of products formed. Any other reagents are in excess and will not all react
Equations for mol, mass, and molar mass
Amount (n,mol)= Mass (m,g)/Molar mass (M,g/mol)
Molar mass is just the relative formula mass (Mr)
Equation for solution concentration
Number of moles (mol) = Concentration (mol⁄dm³ ) × Volume (dm³)
Equation for gas volume
Volume = Moles × 24
Percentage yield equation
% yield= experimental yield (mol or g)/theoretical yield (mol or g)×100
Atom economy equation
% Atom economy= Total Mr of useful products/Total Mr of all reactants×100
Titrations method
Use a volumetric pipette with pipette filler to measure your acid or alkali and place into conical flask Add indicator (methyl orange or phenolphthalein) The other solution, acid or alkali is added to the burette using a filter funnel The solution is added from the burette into the conical flask until the indicator changes colour (end point). This is your first rough titre. The next titres will be added drop-wise around the point where the indicator changed colour in your rough titre Repeat until concordant results are found - 0.1cm³ close to each other and find a mean of the 2 concordant results
How to improve accuracy of titration
Add drop-wise near to the endpoint Repeat and calculate a mean Have a white tile under the flask Swirl the solution
Methyl Orange
Acid: Red Alkali: Yellow End point: Peach/Orange
Phenolphthalein
Acid: Colourless Alkali: Pink End point: [Colour of whichever substance you're adding]