Spec point which is NOT in Triple Science
1:51 know that covalent compounds do not usually conduct electricity
Electric current is a flow of charged particles that can move.
Covalent compounds do not conduct electricity.
Spec point which is NOT in Triple Science
Electric current is a flow of charged particles that can move.
Covalent compounds do not conduct electricity.
Group 1 metals such as potassium, sodium and lithium, react with water to produce a metal hydroxide and hydrogen. For example:
lithium + water → lithium hydroxide + hydrogen
2Li (s) + 2H₂O (l) → 2LiOH (aq) + H₂ (g)
The observations for the reaction of water with either potassium or sodium or lithium have the following similarities:
In each case a metal hydroxide solution is produced.
These similarities in the reactions provide evidence that the 3 metals are in the same group of the Periodic Table (i.e. have the same number of electrons in their outer shell).
Lithium is the first element in group 1 of the Periodic Table. The observations for the reaction of lithium and water are:
Sodium is the second alkali metal in the group. The reaction of sodium and water is more vigorous than lithium’s:
Potassium is the third alkali metal in the group. The reaction of potassium and water is more vigorous than sodium’s:
When the group 1 metals react with air they oxidise, showing a similar trend in reactivity as we go down the group of the Periodic Table.
Therefore, as we go down group 1 (increasing atomic number), the elements become more reactive: Li<Na<K<Rb<Cs<Fr
From the data in the table, it is possible to deduce the properties of francium from the trends in the other group 1 metals.
For example, we can predict that francium will have a melting point around 20⁰C and a density of just over 2g/cm³.
We can also predict that francium will react violently with water, producing francium hydroxide and hydrogen.
Alkali metal | Melting point (⁰C) | Density (g/cm³) | Reaction with water | Products |
---|---|---|---|---|
lithium (Li) | 181 | 0.53 | fizzing | lithium hydroxide + hydrogen |
sodium (Na) | 98 | 0.97 | rapid fizzing | sodium hydroxide + hydrogen |
potassium (K) | 63 | 0.86 | vigorous fizzing and lilac flame | potassium hydroxide + hydrogen |
rubidium (Rb) | 39 | 1.53 | ? | rubidium hydroxide + hydrogen |
caesium(Cs) | 29 | 1.88 | ? | caesium hydroxide + hydrogen |
francium (Fr) | ? | ? | ? | ? |
Element | Colour | State at room temp |
---|---|---|
Chlorine (Cl2) | Green | Gas |
Bromine (Br2) | Red-brown | Liquid |
Iodine (l2) | Grey | Solid |
Chlorine is a toxic gas, so should be handled in a fume cupboard.
If you look at the trends in the physical properties of the halogens, Cl2, Br2, I2 you can make predictions about the properties of the other halogens.
Element | Colour | State at room temp |
---|---|---|
Fluorine (F2) | Yellow | Gas |
Astatine (At2) | Black | Solid |
Group 7 elements are called the Halogens. As you go up group 7 (decreasing atomic number), the elements become more reactive. For example, fluorine is the most reactive and astatine is the least reactive.
A more reactive halogen will displace a less reactive halogen, e.g. chlorine will displace bromine:
By reacting a halogen solution with a potassium halide solution and making observations, the order of their reactivity can be deduced:
Potassium chloride, KCl(aq) | Potassium bromide, KBr(aq) | Potassium iodide, KI(aq) | |
---|---|---|---|
Chlorine, Cl2(aq) | No change | Colourless to orange | Colourless to brown |
Bromine, Br2(aq) | No change | No change | Colourless to brown |
Iodine, I2(aq) | No change | No change | No change |
From the above results, chlorine displaces both bromine and iodine, and bromine displaces iodine. Therefore the order of reactivity is: chlorine is more reactive than bromine, which in turn is more reactive than iodine.
Air is a mixture of different gases.
The abundance of gases in the air is as follows:
Gas | % by volume |
---|---|
Nitrogen, N2 | 78.1 |
Oxygen, O2 | 21.0 |
Argon, Ar | 0.9 |
Carbon dioxide, CO2 | 0.04 |
The following 3 experiments can be used to determine that oxygen (O2) makes up approximately 20% by volume of the composition of air.
Copper
The copper is in excess and uses up the oxygen to form copper oxide (CuO).
All the oxygen in the air is therefore used up, and so the volume of the air decreases by about 20% (the percentage of oxygen in air).
Iron
The iron reacts with the oxygen in the air (rusting).
As long as the iron and water are in excess, the total volume of air enclosed by the apparatus decreases by about a fifth (20%) over several days.
Phosphorus
The phosphorus is lit with a hot wire.
It reacts with the oxygen in the air and causes the water level in the bell jar to rise by about 20%.
Magnesium reacts with oxygen producing a bright white flame leaving behind a white ash of magnesium oxide.
magnesium + oxygen → magnesium oxide
2Mg (s) + O₂ (g) → 2MgO
MgO is a base, which can react with an acid to give a salt and water.
Hydrogen reacts with oxygen in an explosive reaction. This is the basis of the ‘squeak pop’ test for hydrogen in test tube. With larger quantities of hydrogen this explosion can be dangerous.
hydrogen + oxygen → water
2H₂ (g) + O₂ (g) → 2H₂O (l)
Sulfur reacts with oxygen producing a blue flame.
sulfur + oxygen → sulfur dioxide
S (s) + O₂ (g) → SO₂ (g)
When sulfur dioxide (SO₂) dissolves in water it forms an acidic solution of sulfurous acid:
SO₂ (g) + H₂O (l) → H₂SO₃ (aq)
thermal decomposition is the process of breaking down by heating.
On heating metal carbonates thermal decompose into metal oxides and carbon dioxide.
Observation: green powder (CuCO3) changes to a black powder (CuO)
Carbon dioxide (CO2) is a greenhouse gas.
It absorbs infra-red radiation and therefore warms the atmosphere. This leads to global warming.
This may cause climate change.
The following 3 experiments can be used to determine that oxygen (O2) makes up approximately 20% by volume of air.
Copper
The copper is in excess and uses up the oxygen to form copper oxide (CuO).
All the oxygen in the air is therefore used up, and so the volume of the air decreases by about 20% (the percentage of oxygen in air).
Iron
The iron reacts with the oxygen in the air (rusting).
As long as the iron, oxygen and water are all in excess, the total volume of air enclosed by the apparatus decreases by about a fifth (20%) over several days.
Phosphorus
The phosphorus is lit with a hot wire.
It reacts with the oxygen in the air and causes the water level in the bell jar to rise by about 20%.
Some metals are more reactive than others.
The order of reactivity can be determined by adding acid to different metals and observing the rate of reaction.
For example, when hydrochloric acid is added to iron (Fe) then bubbles of hydrogen are produced slowly. However, if the same acid is added to zinc (Zn) then bubbles will be produced more quickly. This tells us that zinc is more reactive than iron.
Instead of using acid, water can be used to test the relative reactivity of metals. However, many metals are too low in the reactivity series to react with water
A metal will displace another metal from its oxide that is lower in the reactivity series. For example, a reaction with magnesium and copper (II) oxide will result in the magnesium displacing the copper from its oxide:
A metal will also displace another metal from its salt that is lower in the reactivity series. For example, the reaction between zinc and copper (II) sulfate solution will result in zinc displacing the copper from its salt:
The blue colour of the copper (II) sulfate solution fades as colourless zinc sulfate solution is formed.
A more reactive metal will displace a less reactive metal.
In addition a more reactive metal will react more vigorously than a less reactive metal.
For example, potassium takes a shorter time to react than sodium:
Iron rusts when oxygen and water are present.
Reaction:
Barrier Methods: Rusting may be prevented by stopping the water and oxygen getting to the iron with a barrier of grease, oil, paint or plastic.
Galvanising: (coating in zinc) also prevents water and oxygen getting to the iron, but with galvanising even if the barrier is broken the more reactive zinc corrodes before the less reactive iron. During the process, the zinc loses electrons to form zinc ions.
Sacrificial Protection: Zinc blocks are attached to iron boat hulls and underground pipelines to act as sacrificial anodes. Zinc is more reactive than iron, so oxygen in the air reacts with the zinc to form a layer of zinc oxide instead of the iron.
Oxidation
Reduction
Redox: A reaction involving oxidation and reduction.
A good way to remember the definitions of oxidation and reduction in terms of electrons is:
Oxidising agent: A substance that gives oxygen or removes electrons (it is itself reduced).
Reducing agent: A substance that takes oxygen or gives electrons (it is itself oxidised).
Metals which are above hydrogen in the reactivity series will react with dilute hydrochloric or sulfuric acid to produce a salt and hydrogen.
metal + acid → salt + hydrogen
For example:
magnesium + hydrochloric acid → magnesium chloride + hydrogen
Mg (s) + 2HCl (aq) → MgCl₂ (aq) + H₂ (g)
This is a displacement reaction.
There is a rapid fizzing and a colourless gas is produced. This gas pops with a lighted splint, showing the gas is hydrogen.
The reaction mixture becomes warm as heat is produced (exothermic).
The magnesium disappears to leave a colourless solution of magnesium chloride.
If more reactive metals are used instead of magnesium the reaction will be faster so the fizzing will be more vigorous and more heat will be produced.
Indicators are substances which change colour in response to a change in pH (acid or alkali).
Indicator | Colour in acidic solution [H+] | Colour in alkaline solution [OH-] |
---|---|---|
Litmus | Red | Blue |
Methyl orange | Red | Yellow |
Phenolphthalein | Colourless | Pink |
Methyl orange is orange in a neutral solution
The pH scale ranges from 0 to 14, and tells you how acidic or how alkaline a solution is.
strongly acidic | weakly acidic | neutral | weakly alkaline | strongly alkaline | |
---|---|---|---|---|---|
pH | 0-3 | 4-6 | 7 | 8-10 | 11-14 |
An indicator is a substance that has more than one colour form depending on the pH.
Universal indicator is a mixture of different dyes which change colour in a gradual way over a range of pH.
An acid is source of hydrogen ions (H+).
An alkali is source of hydroxide ions (OH–).
Metal oxides, metal hydroxides and ammonia (NH₃) are called bases.
Bases neutralise acids by combining with the hydrogen ions in them.
The key reaction is:
acid + base → salt + water
An example of this is:
sulfuric acid + copper oxide → copper sulfate + water
H₂SO₄ + CuO → CuSO₄ + H₂O
Salt | Solubility | Exceptions |
---|---|---|
sodium (Na+), potassium (K+) and ammonium (NH4+) | soluble | none |
nitrates (NO3-) | soluble | none |
chlorides (Cl-) | soluble | silver chloride (AgCl) and lead (II) chloride (PbCl2) |
sulfates (SO42-) | soluble | barium sulfate (BaSO4), calcium sulfate (CaSO4) and lead (II) sulfate (PbSO4) |
carbonates (CO32-) | insoluble | sodium carbonate (Na2CO3), potassium carbonate (K2CO3) and ammonium carbonate ((NH4)2CO3) |
hydroxides (OH-) | insoluble | sodium hydroxide (NaOH), potassium hydroxide (KOH) and calcium hydroxide (Ca(OH)2) (calcium hydroxide is slightly soluble) |
An acid is a proton (H⁺) donor.
A base is a proton (H⁺) acceptor.
A proton is the same as a hydrogen ion. A good way to think about that is to realise that a hydrogen atom is just one proton and zero neutrons surrounded by only one electron. If that atom becomes an ion by the removal of the electron, then only one proton is left.
When sulfuric acid reacts with copper (II) oxide (CuO):
Cu²⁺O²⁻ (s) + H₂SO₄ (aq) → Cu²⁺ (aq) + SO₄²⁻ (aq) + H₂O (l)
H₂SO₄ is an acid. It donates protons (H⁺) to CuO, the base.
An acid is a proton donor.
A base is a proton acceptor.
A proton is the same as a hydrogen ion. A good way to think about that is to realise that a hydrogen atom is just one proton and zero neutrons surrounded by only one electron. If that atom becomes an ion by the removal of the electron, then only one proton is left.
Acid reactions summary
alkali + acid → water + salt
base + acid → water + salt
carbonate + acid → water + salt + carbon dioxide
metal + acid → salt + hydrogen
To assist remembering this list, many pupils find it useful to remember this horrid looking but very effective mnemonic:
AAWS
BAWS
CAWS CoD
MASH
Acids are a source of hydrogen ions (H⁺) when in solution. When the hydrogen in an acid is replaced by a metal, the compound is called a salt. The name of the salt depends on the acid used. For example if sulfuric acid is used then a sulfate salt will be formed.
Parent acid | Formula | Salt | Formula ion |
---|---|---|---|
sulfuric acid | H2SO4 | sulfate | SO42- |
hydrochloric acid | HCl | chloride | Cl- |
nitric acid | HNO3 | nitrate | NO3- |
Acid + Alkali and Acid + Base
A base is a substance that can neutralise an acid, forming a salt and water only.
Alkalis are soluble bases. When they react with acids, a salt and water is formed. The salt formed is often as a colourless solution. Alkalis are a source of hydroxide ions (OH⁻) when in solution.
alkali + acid → water + salt
base + acid → water + salt
Examples of acid + alkali reactions:
Example of an acid + base reaction:
CuO (s) + H₂SO₄ (aq) → CuSO₄ (aq) + H₂O (l)
Acid + Carbonate
carbonate + acid → water + salt + carbon dioxide
A carbonate is a compound made up of metal ions and carbonate ions. Examples of metal carbonates are sodium carbonate, copper carbonate and magnesium carbonate.
When carbonates react with acids, bubbling is observed which is the carbon dioxide being produced. If the acid is in excess the carbonate will disappear.
Examples of acid + carbonate reactions:
Acid + Metal
metal + acid → salt + hydrogen
Metals will react with an acid if the metal is above hydrogen in the reactivity series.
When metals react with acids, bubbling is observed which is the hydrogen being produced. If the acid is in excess the metal will disappear.
Examples of acid + metal reactions:
A base is a substance that neutralises an acid by combining with the hydrogen ions in them to produce water.
A base usually means a metal oxide, a metal hydroxide or ammonia.
Alkalis are bases which are soluble in water.
Some metal oxides are soluble in water and react with it to form solutions of metal hydroxides. For example:
Na₂O (s) + H₂O (l) → 2NaOH (aq)
Apart from this and other group 1 oxides (such as potassium oxide) most other metal oxides are not soluble in water.
One exception is calcium oxide which does dissolve slightly in water to form calcium hydroxide (known as limewater):
CaO (s) + H₂O (l) → Ca(OH)₂ (aq)
Ammonia is another base. Ammonia reacts with water to form ammonium ions and hydroxide ions:
NH₃ (aq) + H₂O (l) ⇋ NH₄⁺ (aq) + OH⁻ (aq)
All the solutions produced here contain hydroxide ions (OH⁻) so they are all alkalis.
Excess Solid Method:
Preparing pure dry crystals of copper sulfate (CuSO4) from copper oxide (CuO) and sulfuric acid (H2SO4)
Step | Explanation |
---|---|
Heat acid (H2SO4) in a beaker | Speeds up the rate of reaction |
Add base (CuO) until in excess (no more copper oxide dissolves) and stir with glass rod | Neutralises all the acid |
Filter the mixture using filter paper and funnel | Removes any excess copper oxide |
Gently heat the filtered solution (CuSO4) | To evaporate some of the water |
until crystals form on a glass rod | Shows a hot saturated solution formed |
Allow the solution to cool so that hydrated crystals form | Copper sulfate less soluble in cold solution |
Remove the crystals by filtration | Removes crystals |
Dry by leaving in a warm place | Evaporates the water |
Excess Solid Method:
Preparing pure dry crystals of copper sulfate (CuSO4) from copper oxide (CuO) and sulfuric acid (H2SO4)
Step | Explanation |
---|---|
Heat acid (H2SO4) in a beaker | Speeds up the rate of reaction |
Add base (CuO) until in excess (no more copper oxide dissolves) and stir with glass rod | Neutralises all the acid |
Filter the mixture using filter paper and funnel | Removes any excess copper oxide |
Gently heat the filtered solution (CuSO4) | To evaporate some of the water |
until crystals form on a glass rod | Shows a hot saturated solution formed |
Allow the solution to cool so that hydrated crystals form | Copper sulfate less soluble in cold solution |
Remove the crystals by filtration | Removes crystals |
Dry by leaving in a warm place | Evaporates the water |
Test for hydrogen gas (H2)
Test for carbon dioxide (CO2)
Tests for gases
Gas | Test | Result if gas present |
---|---|---|
hydrogen (H2) | Use a lit splint | Gas pops |
oxygen (O2) | Use a glowing splint | Glowing splint relights |
carbon dioxide (CO2) | Bubble the gas through limewater | Limewater turns cloudy |
ammonia (NH3) | Use red litmus paper | Turns damp red litmus paper blue |
chlorine (Cl2) | Use damp litmus paper | Turns damp litmus paper white (bleaches) |
A flame test is used to show the presence of certain metal ions (cations) in a compound.
Properties of the platinum or nichrome wire is:
When put into a roaring bunsen burner flame on a nichrome wire, compounds containing certain cations will give specific colours as follows.
Ion | Colour in flame test |
---|---|
lithium (Li⁺) | red |
sodium (Na⁺) | yellow |
potassium (K⁺) | lilac |
calcium (Ca²⁺) | orange-red |
copper (II) (Cu²⁺) | blue-green |
Describe tests for the cations Cu2+, Fe2+ and Fe3+, using sodium hydroxide solution
First, add sodium hydroxide (NaOH), then observe the colour:
Describe tests for anions: Carbonate ions (CO32-)
Describe tests for anions: Halide ions (Cl–, Br– and I–)
Underneath are the tests for:
chloride ion test, bromide ion test, iodide ion test, sulfate ion test, carbonate ion test
Describe tests for anions: Sulfate ions (SO42–)
Describe tests for anions: Carbonate ions (CO32-)
Add anhydrous copper (II) sulfate (CuSO4) to a sample.
If water is present the anhydrous copper (II) sulfate will change from white to blue.
If the sample is pure water it will boil at 100oC
Exothermic: chemical reaction in which heat energy is given out.
Endothermic: chemical reaction in which heat energy is taken in.
(So, in an exothermic reaction the heat exits from the chemicals so temperature rises)
Calorimetry allows for the measurement of the amount of energy transferred in a chemical reaction to be calculated.
EXPERIMENT1: Displacement, dissolving and neutralisation reactions
Example: magnesium displacing copper from copper(II) sulfate
Method:
Initial temp. of solution (oC) | Maximium temp. of solution (oC) | Temperature rise (oC) |
---|---|---|
24.2 | 56.7 | 32.5 |
Note: mass of 50 cm3 of solution is 50 g
The cup used is polystyrene because:
polystyrene is an insulator which reduces heats loss
EXPERIMENT2: Combustion reactions
To measure the amount of energy produced when a fuel is burnt, the fuel is burnt and the flame is used to heat up some water in a copper container
Example: ethanol is burnt in a small spirit burner
Method:
Mass of water (g) | Initial temp of water (oC) | Maximum temp of water (oC) | Temperature rise (oC) | Initial mass of spirit burner + ethanol (g) | Final mass of spirit burner + ethanol (g) | Mass of ethanol burnt (g) |
---|---|---|---|---|---|---|
100 | 24.2 | 54.2 | 30.0 | 34.46 | 33.68 | 0.78 |
The amount of energy produced per gram of ethanol burnt can also be calculated:
Calorimetry allows for the measurement of the amount of energy transferred in a chemical reaction to be calculated.
EXPERIMENT1: Displacement, dissolving and neutralisation reactions
Example: magnesium displacing copper from copper(II) sulfate
Method:
Initial temp. of solution (oC) | Maximium temp. of solution (oC) | Temperature rise (oC) |
---|---|---|
24.2 | 56.7 | 32.5 |
Note: mass of 50 cm3 of solution is 50 g
EXPERIMENT2: Combustion reactions
To measure the amount of energy produced when a fuel is burnt, the fuel is burnt and the flame is used to heat up some water in a copper container
Example: ethanol is burnt in a small spirit burner
Method:
Mass of water (g) | Initial temp of water (oC) | Maximum temp of water (oC) | Temperature rise (oC) | Initial mass of spirit burner + ethanol (g) | Final mass of spirit burner + ethanol (g) | Mass of ethanol burnt (g) |
---|---|---|---|---|---|---|
100 | 24.2 | 54.2 | 30.0 | 34.46 | 33.68 | 0.78 |
The amount of energy produced per gram of ethanol burnt can also be calculated:
Calorimetry allows for the measurement of the amount of energy transferred in a chemical reaction to be calculated.
EXPERIMENT1: Displacement, dissolving and neutralisation reactions
Example: magnesium displacing copper from copper(II) sulfate
Method:
Initial temp. of solution (oC) | Maximium temp. of solution (oC) | Temperature rise (oC) |
---|---|---|
24.2 | 56.7 | 32.5 |
Note: mass of 50 cm3 of solution is 50 g
EXPERIMENT2: Combustion reactions
To measure the amount of energy produced when a fuel is burnt, the fuel is burnt and the flame is used to heat up some water in a copper container
Example: ethanol is burnt in a small spirit burner
Method:
Mass of water (g) | Initial temp of water (oC) | Maximum temp of water (oC) | Temperature rise (oC) | Initial mass of spirit burner + ethanol (g) | Final mass of spirit burner + ethanol (g) | Mass of ethanol burnt (g) |
---|---|---|---|---|---|---|
100 | 24.2 | 54.2 | 30.0 | 34.46 | 33.68 | 0.78 |
The amount of energy produced per gram of ethanol burnt can also be calculated:
The rate of a chemical reaction can be measured either by how quickly reactants are used up or how quickly the products are formed.
The rate of reaction can be calculated using the following equation:
The units for rate of reaction will usually be grams per min (g/min)
An investigation of the reaction between marble chips and hydrochloric acid:
Marble chips, calcium carbonate (CaCO3) react with hydrochloric acid (HCl) to produce carbon dioxide gas. Calcium chloride solution is also formed.
Using the apparatus shown the change in mass of carbon dioxide can be measure with time.
As the marble chips react with the acid, carbon dioxide is given off.
The purpose of the cotton wool is to allow carbon dioxide to escape, but to stop any acid from spraying out.
The mass of carbon dioxide lost is measured at intervals, and a graph is plotted:
Experiment to investigate the effects of changes in surface area of solid on the rate of a reaction:
The experiment is repeated using the same mass of chips, but this time the chips are larger, i.e. have a smaller surface area.
Since the surface area is smaller, the rate of reaction is less.
Both sets of results are plotted on the same graph.
If instead the chips were smashed into powder (and again same mass of chips used) the surface area would be much larger and so the rate of reaction higher (steeper line on graph).
Experiment to investigate the effects of changes in concentration of solutions on the rate of a reaction:
The experiment is again repeated using the exact same quantities of everything but this time with half the concentration of acid. The marble chips must however be in excess. The reaction with the half the concentration of acid happens slower and produces half the amount of carbon dioxide.
Experiment to investigate the effects of changes in temperature on the rate of a reaction:
The experiment is once again repeated using the exact same quantities of everything but this time at a higher temperature. The reaction with the higher temperature happens faster.
Experiment to investigate the effects of the use of a catalyst on the rate of a reaction:
Hydrogen peroxide naturally decomposes slowly producing water and oxygen gas.
Manganese (IV) oxide can be used as a catalyst to speed up the rate of reaction.
The rate of reaction can be measured by measuring the volume of oxygen produced at regular intervals using a gas syringe.
Both sets of results are plotted on the same graph.
Experiment to investigate the reaction between varying concentrations of sodium thiosulfate and hydrochloric acid
Sodium thiosulfate (Na2S2O3) and hydrochloric acid (HCl) are both colourless solutions. They react to form a yellow precipitate of sulfur.
sodium thiosulfate + hydrochloric acid → sodium chloride + sulfur dioxide + sulfur + water
Na2S2O3(aq) + 2HCl(aq) → 2NaCl(aq) + SO2(g) + S(s) + H2O(l)
To investigate the effects of changes in concentration of sodium thiosulfate on the rate of a reaction, the conical flask is placed above a cross. The reaction mixture is observed from directly above and the time for a cross to disappear is measured. The cross disappears because a precipitate of sulfur is formed.
In order to change the concentration of sodium thiosulfate, the volumes of sodium thiosulfate and water are varied (see results table). However the total volume of solution must always be kept the same as to ensure that the depth of the solution remains constant.
In this reaction, sulfur dioxide gas (SO2), which is poisonous is produced therefore the experiment must be carried out in a well ventilated room.
The results are recorded in the table below and then plotted onto a graph.
Volume of Na2S2O3(aq) (cm3) | Volume of water (cm3) | Concentration of Na2S2O3(aq) (mol/dm3) | Time taken for cross to disappear (s) | Rate of reaction (s-1) (1/time) |
---|---|---|---|---|
50 | 0 | 0.10 | 45 | 0.0222 |
40 | 10 | 0.08 | 60 | 0.0167 |
30 | 20 | 0.06 | 80 | 0.0125 |
20 | 30 | 0.04 | 13 | 0.0769 |
10 | 40 | 0.02 | 255 | 0.0039 |
The graph shows that the rate of reaction is directly proportional to the concentration.
The experiment can also be repeated to show how temperature affects the rate of reaction.
In this experiment the concentration of sodium thiosulfate is kept constant but heated to range of different temperatures.
As a rough approximation, the rate of reaction doubles for every 10oC temperature rise.
Increasing the surface area of a solid increases the rate of a reaction.
Increasing the concentration of a solution increases the rate of a reaction.
Increasing the pressure of a gas increases the rate of a reaction.
Increasing the temperature increases the rate of a reaction.
Using a catalyst increases the rate of a reaction.
Increasing the surface area of a solid:
Increasing the concentration of a solution or pressure of a gas:
Increasing the temperature:
A catalyst is a substance that increases the rate of a reaction, but is chemically unchanged at the end of the reaction.