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Science 0654 (2025-): Chemistry

ScienceGrades 09, 10, 11, 12CSP ID: 4F659977BE874E52A80AE208B037248CStandards: 411

Standards

Showing 411 of 411 standards.

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C1

Depth 0

States of matter

C2

Depth 0

Atoms, elements and compounds

C3

Depth 0

Stoichiometry

C4

Depth 0

Electrochemistry

C5

Depth 0

Chemical energetics

C6

Depth 0

Chemical reactions

C7

Depth 0

Acids, bases and salts

C8

Depth 0

The Periodic Table

C9

Depth 0

Metals

C10

Depth 0

Chemistry of the environment

C11

Depth 0

Organic chemistry

C12

Depth 0

Experimental techniques and chemical analysis

C1.1

Depth 1

Solids, liquids and gases

C1.2

Depth 1

Diffusion

C2.1

Depth 1

Elements, compounds and mixtures

C2.2

Depth 1

Atomic structure and the Periodic Table

C2.3

Depth 1

Isotopes

C2.4

Depth 1

lons and ionic bonds

C2.5

Depth 1

Simple molecules and covalent bonds

C2.6

Depth 1

Giant covalent structure

C2.7

Depth 1

Metallic bonding

C3.1

Depth 1

Formulas

C3.2

Depth 1

Relative masses of atoms and molecules

C3.3

Depth 1

The mole and the Avogadro constant

C4.1

Depth 1

Electrolysis

C4.2

Depth 1

Hydrogen-oxygen fuel cells

C5.1

Depth 1

Exothermic and endothermic reactions

C6.1

Depth 1

Physical and chemical changes

C6.2

Depth 1

Rate of reaction

C6.3

Depth 1

Redox

C7.1

Depth 1

The characteristic properties of acids and bases

C7.2

Depth 1

Oxides

C7.3

Depth 1

Preparation of salts

C8.1

Depth 1

Arrangement of elements

C8.2

Depth 1

Group I properties

C8.3

Depth 1

Group VII properties

C8.4

Depth 1

Transition elements

C8.5

Depth 1

Noble gases

C9.1

Depth 1

Properties of metals

C9.2

Depth 1

Uses of metals

C9.3

Depth 1

Alloys and their properties

C9.4

Depth 1

Reactivity series

C9.5

Depth 1

Corrosion of metals

C9.6

Depth 1

Extraction of metals

C10.1

Depth 1

Water

C10.2

Depth 1

Air quality and climate

C11.1

Depth 1

Formulas and terminology

C11.2

Depth 1

Naming organic compounds

C11.3

Depth 1

Fuels

C11.4

Depth 1

Alkanes

C11.5

Depth 1

Alkenes

C11.6

Depth 1

Alcohols

C11.7

Depth 1

Polymers

C12.1

Depth 1

Experimental design

C12.2

Depth 1

Acid-base titrations

C12.3

Depth 1

Chromatography

C12.4

Depth 1

Separation and purification

C12.5

Depth 1

Identification of ions and gases

C1.1.1

Depth 2

State the distinguishing properties of solids, liquids and gases

C1.1.2

Depth 2

Describe the structure of solids, liquids and gases in terms of particle separation, arrangement and motion

C1.1.3

Depth 2

Describe changes of state in terms of melting, boiling, evaporating, freezing and condensing

C1.1.4

Depth 2

Describe the effects of temperature and pressure on the volume of a gas

C1.1.5S

Depth 2

Explain changes of state in terms of kinetic particle theory, including the interpretation of heating and cooling curves

C1.1.6S

Depth 2

Explain, in terms of kinetic particle theory, the effects of temperature and pressure on the volume of a gas

C1.2.1

Depth 2

Describe and explain diffusion in terms of kinetic particle theory

C1.2.2S

Depth 2

Describe and explain the effect of relative molecular mass on the rate of diffusion of gases

C2.1.1

Depth 2

Describe the differences between elements, compounds and mixtures

C2.2.1

Depth 2

Describe the structure of the atom as a central nucleus containing neutrons and protons, surrounded by electrons in shells

C2.2.2

Depth 2

State the relative charges and relative masses of a proton, a neutron and an electron

C2.2.3

Depth 2

Define proton number / atomic number as the number of protons in the nucleus of an atom

C2.2.4

Depth 2

Define mass number/ nucleon number as the total number of protons and neutrons in the nucleus of an atom

C2.2.5

Depth 2

Determine the electronic configuration of elements with proton number 1 to 20, e.g. 2,8,3

C2.2.6

Depth 2

State that:

C2.3.1

Depth 2

Define isotopes as different atoms of the same element that have the same number of protons but different numbers of neutrons

C2.3.2

Depth 2

Interpret and use symbols for atoms, e.g. (symbol for, including atomic number and mass) Carbon, and ions, e.g. Chloride ion

C2.3.3S

Depth 2

State that isotopes of the same element have the same chemical properties because they have the same number of electrons and therefore the same electronic configuration

C2.4.1

Depth 2

Describe the formation of positive ions, known as cations, and negative ions, known as anions

C2.4.2

Depth 2

State that an ionic bond is a strong electrostatic attraction between oppositely charged ions

C2.4.3

Depth 2

Describe the formation of ionic bonds between elements from Group I and Group VIll, including the use of dot-and-cross diagrams

C2.4.4

Depth 2

Describe the properties of ionic compounds: 

C2.4.5S

Depth 2

Describe the formation of ionic bonds between ions of metallic and non-metallic elements, including the use of dot-and-cross diagrams

C2.4.6S

Depth 2

Explain in terms of structure and bonding the properties of ionic compounds:

C2.4.7S

Depth 2

Describe the giant lattice structure of ionic compounds as a regular arrangement of alternating positive and negative ions, exemplified by sodium chloride

C2.5.1

Depth 2

State that a covalent bond is formed when a pair of electrons is shared between two atoms leading to noble gas electronic configurations

C2.5.2

Depth 2

Describe the formation of covalent bonds in simple molecules, including H2, Cl2, H2O, CH4, NH3 and HCl. Use dot-and cross diagrams to show the electronic configurations in these molecules

C2.5.3

Depth 2

Describe in terms of structure and bonding the properties of simple molecular compounds:

C2.5.4S

Depth 2

Describe the formation of covalent bonds in simple molecules, including СН3ОН, С2H4, O2, CO2, and Na. Use dot-and-cross diagrams to show the electronic configurations in these molecules

C2.5.5S

Depth 2

Explain in terms of structure and bonding the properties of simple molecular compounds:

C2.6.1

Depth 2

Describe the giant covalent structures of graphite and diamond

C2.6.2S

Depth 2

Relate the structures and bonding of graphite and diamond to their uses, limited to:

C2.7.1

Depth 2

Describe metallic bonding as the electrostatic attraction between the positive ions in a giant metallic lattice and a 'sea' of delocalised electrons

C2.7.2S

Depth 2

Explain in terms of structure and bonding the properties of metals:

C3.1.1

Depth 2

State the formulas of the elements and compounds named in the subject content

C3.1.2

Depth 2

Define the molecular formula of a compound as the number and type of atoms in one molecule

C3.1.3

Depth 2

Deduce the formula of a simple molecular compound from the relative numbers of atoms present in a model or a diagrammatic representation

C3.1.4

Depth 2

Construct word equations to show how reactants form products

C3.1.5

Depth 2

Balance and interpret simple symbol equations, including state symbols

C3.1.6S

Depth 2

Deduce the formula of an ionic compound from the relative numbers of the ions present in a model or a diagrammatic representation or from the charges on the ions

C3.1.7S

Depth 2

Construct symbol equations with state symbols, including ionic equations

C3.1.8S

Depth 2

Deduce the symbol equation with state symbols for a chemical reaction, given relevant information

C3.2.1

Depth 2

Describe relative atomic mass, Ar, as the average mass of the isotopes of an element compared to 1/12th of the mass of an atom of Carbon-12

C3.2.2

Depth 2

Define relative molecular mass, Mr, as the sum of the relative atomic masses. Relative formula mass, Mr will be used for ionic compounds

C3.2.3

Depth 2

Calculate reacting masses in simple proportions (calculations will not involve the mole concept)

C3.3.1

Depth 2

State that concentration can be measured in g/dm3

C3.3.2S

Depth 2

State that the mole, mol, is the unit of amount of substance and that one mole contains 6.02 × 10^23 particles, e.g. atoms, ions, molecules; this number is the Avogadro constant

C3.3.3S

Depth 2

se the relationship - Amount of substance (mol) = mass (g) / molar mass (g/mol) to calculate:

C3.3.4S

Depth 2

Use the molar gas volume, taken as 24 dm3 at room temperature and pressure, r.t.p., in calculations involving gases

C3.3.5S

Depth 2

Calculate stoichiometric reacting masses, limiting reactants, volumes of gases at r.t.p., including conversion between cm3 and dm3

C4.1.1

Depth 2

Define electrolysis as the decomposition of an ionic compound, when molten or in aqueous solution, by the passage of an electric current

C4.1.2

Depth 2

Identify in simple electrolytic cells:

C4.1.3

Depth 2

Identify the products formed at the electrodes and describe the observations made during the electrolysis of:

C4.1.4S

Depth 2

Describe the transfer of charge during electrolysis:

C4.1.5S

Depth 2

Identify the products formed at the electrodes and describe the observations made during the electrolysis of aqueous copper(II) sulfate using carbon/ graphite electrodes and when using copper electrodes

C4.1.6S

Depth 2

State that metals or hydrogen are formed at the cathode and that non-metals other than hydrogen) are formed at the anode

C4.1.7S

Depth 2

Predict the identity of the products at each electrode for the electrolysis of a binary compound in the molten state

C4.1.8S

Depth 2

Construct ionic half-equations for reactions at the cathode (showing gain of electrons as a reduction reaction)

C4.2.1

Depth 2

State that a hydrogen-oxygen fuel cell uses hydrogen and oxygen to produce electricity with water as the only chemical product

C4.2.2S

Depth 2

Describe the advantages and disadvantages of using hydrogen-oxygen fuel cells in comparison with gasoline/ petrol engines in vehicles

C5.1.1

Depth 2

State that an exothermic reaction transfers thermal energy to the surroundings leading to an increase in the temperature of the surroundings

C5.1.2

Depth 2

State that an endothermic reaction takes in thermal energy from the surroundings leading to a decrease in the temperature of the surroundings

C5.1.3S

Depth 2

Interpret reaction pathway diagrams showing exothermic and endothermic reactions

C5.1.4S

Depth 2

State that the transfer of thermal energy during a reaction is called the enthalpy change, ∆H, of the reaction. ∆H is negative for exothermic reactions and positive for endothermic reactions

C5.1.5S

Depth 2

Define activation energy, Ea, as the minimum energy that colliding particles must have to react

C5.1.6S

Depth 2

Draw and label reaction pathway diagrams for exothermic and endothermic reactions using information provided, to include:

C5.1.7S

Depth 2

State that bond breaking is an endothermic process and bond making is an exothermic process

C6.1.1

Depth 2

Identify physical and chemical changes, and understand the differences between them

C6.2.1

Depth 2

Describe the effect on the rate of reaction of:

C6.2.2

Depth 2

State that a catalyst increases the rate of a reaction and is unchanged at the end of a reaction

C6.2.3

Depth 2

Describe practical methods for investigating the rate of a reaction including change in mass of a reactant or product and the formation of a gas

C6.2.4

Depth 2

Interpret data, including graphs, from rate of reaction experiments

C6.2.5S

Depth 2

Explain the effect on the rate of reaction of: 

C6.2.6S

Depth 2

State that a catalyst decreases the activation energy, Ea, of a reaction

C6.2.7S

Depth 2

Describe collision theory in terms of:

C6.3.1

Depth 2

Define redox reactions as involving simultaneous oxidation and reduction

C6.3.2

Depth 2

Define oxidation as gain of oxygen and reduction as loss of oxygen

C6.3.3

Depth 2

Identify redox reactions as reactions involving gain and loss of oxygen

C6.3.4

Depth 2

Identity oxidation and reduction in redox reactions. (Oxidation number limited to its use to name ions, e.g. iron(II), iron(III), copper(II).)

C6.3.5S

Depth 2

Define oxidation in terms of:

C6.3.6S

Depth 2

Define reduction in terms of:

C7.1.1

Depth 2

Describe the characteristic properties of acids in terms of their reactions with:

C7.1.2

Depth 2

Describe acids in terms of their effect on the indicators:

C7.1.3

Depth 2

State that bases are oxides or hydroxides of metals and that alkalis are soluble bases

C7.1.4

Depth 2

Describe the characteristic properties of bases in terms of their reactions with acids

C7.1.5

Depth 2

Describe alkalis in terms of their effect on the indicators:

C7.1.6

Depth 2

Describe how to compare neutrality, relative acidity and relative alkalinity in terms of colour and pH using universal indicator

C7.1.7

Depth 2

Describe the neutralisation reaction between an acid and an alkali to produce a salt and water (the ionic equation for this reaction is not required)

C7.2.1

Depth 2

Classify oxides as either acidic, including SO2 and CO2, or basic, including CuO and Cao, related to metallic and non-metallic character

C7.2.2S

Depth 2

Describe amphoteric oxides as oxides that react with acids and with bases to produce a salt and water

C7.2.3S

Depth 2

Classify Al2O3 and ZnO as amphoteric oxides

C7.3.1

Depth 2

Describe the preparation, separation and purification of soluble salts by reaction of an acid with:

C7.3.2

Depth 2

Define a hydrated substance as a substance that is chemically combined with water and an anhydrous substance as a substance containing no water

C7.3.3S

Depth 2

Describe the preparation of insoluble salts by precipitation (the general solubility rules for salts are not required)

C8.1.1

Depth 2

Describe the Periodic Table as an arrangement of elements in periods and groups and in order of increasing proton number/ atomic number

C8.1.2

Depth 2

Describe the change from metallic to non-metallic character across a period

C8.1.3

Depth 2

Explain similarities in the chemical properties of elements in the same group of the Periodic Table in terms of their electronic configuration

C8.1.4S

Depth 2

Identity trends in groups, given information about the elements

C8.2.1

Depth 2

Describe the Group I alkali metals, lithium, sodium and potassium, as relatively soft metals with general trends down the group, limited to:

C8.2.2

Depth 2

Predict the properties of other elements in Group I, given information about the elements

C8.3.1

Depth 2

Describe the Group VII halogens, chlorine, bromine and iodine, as diatomic non-metals with general trends down the group, limited to:

C8.3.2

Depth 2

State the appearance of the halogens at room temperature and pressure, r.t.p., as:

C8.3.3S

Depth 2

Describe and explain the displacement reactions of halogens with other halide ions

C8.3.4S

Depth 2

Predict the properties of other elements in Group VII, given information about the elements

C8.4.1

Depth 2

Describe the transition elements as metals that:

C8.5.1

Depth 2

Describe the Group VIll noble gases as unreactive, monatomic gases and explain this in terms of electronic configuration

C9.1.1

Depth 2

Compare the general physical properties of metals and non-metals, including:

C9.1.2

Depth 2

Describe the general chemical properties of metals, limited to their reactions with:

C9.2.1

Depth 2

Describe the uses of metals in terms of their physical properties, including:

C9.3.1

Depth 2

Describe alloys as mixtures of a metal with other elements, including:

C9.3.2

Depth 2

State that alloys can be harder and stronger than the pure metals and are more useful

C9.3.3

Depth 2

Describe the use of alloys in terms of their physical properties, including stainless steel in cutlery because of its hardness and resistance to rusting 

C9.3.4

Depth 2

Identify representations of alloys from diagrams of structure

C9.3.5S

Depth 2

Explain in terms of structure how alloys can be harder and stronger than the pure metals because the different sized atoms in alloys mean the layers can no longer slide over each other

C9.4.1

Depth 2

State the order of the reactivity series as: potassium, sodium, calcium, magnesium, aluminium, carbon, zinc, iron, hydrogen, copper, silver, gold

C9.4.2

Depth 2

Describe the reactions, if any, of:

C9.4.3

Depth 2

Deduce an order of reactivity from a given set of experimental results

C9.4.4S

Depth 2

Describe the relative reactivities of metals in terms of their tendency to form positive ions, by displacement reactions, if any, with the aqueous ions of magnesium, zinc, iron, copper and silver

C9.5.1

Depth 2

State the conditions required for the rusting of iron (presence of oxygen and water)

C9.5.2

Depth 2

State some common barrier methods, including painting, greasing and coating with plastic

C9.5.3

Depth 2

Describe how barrier methods prevent rusting by excluding oxygen and water

C9.5.4S

Depth 2

Describe the use of zinc in galvanising steel as an example of a barrier method and sacrificial protection

C9.5.5S

Depth 2

Explain sacrificial protection in terms of the reactivity series and in terms of electron loss

C9.6.1

Depth 2

Describe the ease in obtaining metals from their ores, related to the position of the metal in the reactivity series

C9.6.2

Depth 2

State that iron from hematite is extracted by reduction of iron(IIl) oxide in the blast furnace

C9.6.3

Depth 2

State that main ore of aluminium is bauxite and that aluminium is extracted by electrolysis

C9.6.4S

Depth 2

Describe the extraction of iron from hematite in the blast furnace, limited to:

C10.1.1

Depth 2

Describe chemical tests for the presence of water using anhydrous cobalt(II) chloride and anhydrous copper(Il) sulfate

C10.1.2

Depth 2

Describe how to test for the purity of water using melting point and boiling point

C10.1.3

Depth 2

State that distilled water is used in practical chemistry rather than tap water because it contains fewer chemical impurities

C10.1.4

Depth 2

Describe the treatment of the domestic water supply in terms of:

C10.2.1

Depth 2

State the composition of clean, dry air as approximately 78% nitrogen, N2, 21% oxygen, O2, and the remainder as a mixture of noble gases and carbon dioxide, CO2 

C10.2.2

Depth 2

State the source of each of these air pollutants, limited to:

C10.2.3

Depth 2

State the adverse effect of these air pollutants, limited to:

C10.2.4

Depth 2

State and explain strategies to reduce the effects of climate change:

C10.2.5S

Depth 2

State and explain strategies to reduce the effects of acid rain: reducing emissions of sulfur dioxide by using low-sulfur fuels and flue gas desulfurisation with calcium oxide

C10.2.6S

Depth 2

Describe how the greenhouse gases carbon dioxide and methane cause global warming, limited to:

C10.2.7S

Depth 2

Explain how oxides of nitrogen form in car engines and describe their removal by catalytic converters, limited to: 2CO + 2NO → 2CO2 + N2

C11.1.1

Depth 2

Draw and interpret the displayed formula of a molecule to show all the atoms and all the bonds

C11.1.2

Depth 2

State that a saturated compound has molecules in which all carbon-carbon bonds are single bonds

C11.1.3

Depth 2

State that an unsaturated compound has molecules in which one or more carbon-carbon bonds are not single bonds

C11.1.4S

Depth 2

State that a homologous series is a family of similar compounds with similar chemical properties

C11.1.5S

Depth 2

Describe the general characteristics of a homologous series as:

C11.2.1

Depth 2

Name and draw the displayed formulas of: 

C11.2.2

Depth 2

State the type of compound present, given a chemical name ending in -ane, -ene or -ol, or from a molecular formula or displayed formula

C11.2.3S

Depth 2

Name and draw the structural formulas and displayed formulas of unbranched: 

C11.3.1

Depth 2

Name the fossil fuels: coal, natural gas and petroleum

C11.3.2

Depth 2

Name methane as the main constituent of natural gas

C11.3.3

Depth 2

State that hydrocarbons are compounds that contain hydrogen and carbon only

C11.3.4

Depth 2

State that petroleum is a mixture of hydrocarbons

C11.3.5

Depth 2

Describe the separation of petroleum into useful fractions by fractional distillation

C11.3.6

Depth 2

Name the uses of the fractions as:

C11.3.7S

Depth 2

Describe how the properties of fractions obtained from petroleum change from the bottom to the top of the fractionating column, limited to:

C11.4.1

Depth 2

State that the bonding in alkanes is single covalent and that alkanes are saturated hydrocarbons

C11.4.2

Depth 2

Describe the properties of alkanes as being generally unreactive, except in terms of combustion

C11.5.1

Depth 2

State that the bonding in alkenes includes a double carbon-carbon covalent bond and that alkenes are unsaturated hydrocarbons

C11.5.2

Depth 2

Describe the test to distinguish between saturated and unsaturated hydrocarbons by their reaction with aqueous bromine

C11.5.3

Depth 2

Describe the manufacture of alkenes and hydrogen by the cracking of larger alkane molecules using a high temperature and a catalyst

C11.5.4S

Depth 2

Describe the properties of alkenes in terms of addition reactions with:

C11.6.1

Depth 2

Describe the complete combustion of ethanol

C11.6.2

Depth 2

State the uses of ethanol as: 

C11.7.1

Depth 2

Define polymers as large molecules built up from many smaller molecules called monomers

C11.7.2

Depth 2

Describe the formation of poly(ethene) as an example of addition polymerisation using ethene monomers

C11.7.3S

Depth 2

Identify the repeat units in addition polymers and in condensation polymers

C11.7.4S

Depth 2

Deduce the structure or repeat unit of an addition polymer from a given alkene and vice versa

C11.7.5S

Depth 2

Describe the differences between addition and condensation polymerisation

C11.7.6S

Depth 2

Describe and draw the structure of nylon, a polyamide

C12.1.1

Depth 2

Name appropriate apparatus for the measurement of time, temperature, mass and volume, including:

C12.1.2

Depth 2

Describe a:

C12.2.1

Depth 2

Describe an acid-base titration to include the use of a: 

C12.2.2

Depth 2

Describe how to identify the end-point of a titration using an indicator

C12.3.1

Depth 2

Describe how paper chromatography is used to separate mixtures of soluble coloured substances, using a suitable solvent

C12.3.2

Depth 2

Interpret simple chromatograms to identify: 

C12.3.3S

Depth 2

State and use the equation for Rf: Rf = Distance travelled by the substance / Distance travelled by solvent

C12.4.1

Depth 2

Describe and explain methods of separation and purification using:

C12.4.2

Depth 2

Suggest suitable separation and purification techniques, given information about the substances involved

C12.4.3

Depth 2

Identify substances and assess their purity from melting point and boiling point information

C12.5.1

Depth 2

Describe tests to identify the anions:

C12.5.2

Depth 2

Describe tests using aqueous sodium hydroxide and aqueous ammonia to identify the aqueous cations:

C12.5.3

Depth 2

Describe tests to identify the gases:

C12.5.4

Depth 2

Describe the use of a flame test to identify the cations:

C2.2.6.a

Depth 3

Group Vill noble gases have a full outer shell

C2.2.6.b

Depth 3

the number of outer-shell electrons is equal to the group number in Groups I to VII

C2.2.6.c

Depth 3

the number of occupied electron shells is equal to the period number

C2.4.4.a

Depth 3

high melting points and boiling points 

C2.4.4.b

Depth 3

good electrical conductivity when aqueous or molten and poor when solid

C2.4.4.c

Depth 3

generally soluble in water

C2.4.6S.a

Depth 3

high melting points and boiling points

C2.4.6S.b

Depth 3

good electrical conductivity when aqueous or molten and poor when solid

C2.5.3.a

Depth 3

low melting points and boiling points 

C2.5.3.b

Depth 3

poor electrical conductivity

C2.5.5S.a

Depth 3

low melting points and boiling points in terms of weak intermolecular forces (specific types of intermolecular forces are not required) 

C2.5.5S.b

Depth 3

poor electrical conductivity

C2.6.2S.a

Depth 3

graphite as a lubricant and as an electrode

C2.6.2S.b

Depth 3

diamond in cutting tools

C2.7.2S.a

Depth 3

good electrical conductivity

C2.7.2S.b

Depth 3

malleability

C3.3.3S.a

Depth 3

amount of substance (b) mass 

C3.3.3S.b

Depth 3

molar mass

C3.3.3S.c

Depth 3

relative atomic mass or relative molecular/ formula mass

C4.1.2.a

Depth 3

the anode as the positive electrode

C4.1.2.b

Depth 3

the cathode as the negative electrode 

C4.1.2.c

Depth 3

the electrolyte as the molten or aqueous substance that undergoes electrolysis

C4.1.3.a

Depth 3

molten lead(II) bromide

C4.1.3.b

Depth 3

concentrated aqueous sodium chloride

C4.1.3.c

Depth 3

dilute sulfuric acid using inert electrodes made of platinum or carbon/ graphite

C4.1.4S.a

Depth 3

the movement of electrons in the external circuit

C4.1.4S.b

Depth 3

the loss or gain of electrons at the electrodes

C4.1.4S.c

Depth 3

the movement of ions in the electrolyte

C5.1.6S.a

Depth 3

reactants

C5.1.6S.b

Depth 3

products

C5.1.6S.c

Depth 3

overall energy change of the reaction, ∆H (d) activation energy, Ea

C6.2.1.a

Depth 3

changing the concentration of solutions

C6.2.1.b

Depth 3

changing the pressure of gases 

C6.2.1.c

Depth 3

changing the surface area of solids 

C6.2.1.d

Depth 3

changing the temperature

C6.2.1.e

Depth 3

adding or removing a catalyst

C6.2.5S.a

Depth 3

changing the concentration of solutions

C6.2.5S.b

Depth 3

changing the pressure of gases 

C6.2.5S.c

Depth 3

changing the surface area of solids 

C6.2.5S.d

Depth 3

changing the temperature 

C6.2.5S.e

Depth 3

adding or removing a catalyst using collision theory 

C6.2.7S.a

Depth 3

number of particles per unit volume

C6.2.7S.b

Depth 3

frequency of collisions between particles

C6.2.7S.c

Depth 3

kinetic energy of particles 

C6.2.7S.d

Depth 3

activation energy, Ea

C6.3.5S.a

Depth 3

loss of electrons

C6.3.5S.b

Depth 3

an increase in oxidation number (determination of oxidation numbers is not required)

C6.3.6S.a

Depth 3

gain of electrons

C6.3.6S.b

Depth 3

a decrease in oxidation number (determination of oxidation numbers is not required)

C7.1.1.a

Depth 3

metals

C7.1.1.b

Depth 3

bases

C7.1.1.c

Depth 3

carbonates

C7.1.2.a

Depth 3

litmus

C7.1.2.b

Depth 3

methyl orange

C7.1.5.a

Depth 3

litmus

C7.1.5.b

Depth 3

methyl orange

C7.3.1.a

Depth 3

an alkali by titration

C7.3.1.b

Depth 3

excess metal

C7.3.1.c

Depth 3

excess insoluble base

C7.3.1.d

Depth 3

excess insoluble carbonate (the general solubility rules for salts are not required)

C8.2.1.a

Depth 3

decreasing melting point 

C8.2.1.b

Depth 3

increasing density 

C8.2.1.c

Depth 3

increasing reactivity with water

C8.3.1.a

Depth 3

increasing density 

C8.3.1.b

Depth 3

decreasing reactivity

C8.3.2.a

Depth 3

chlorine, a pale yellow-green gas 

C8.3.2.b

Depth 3

bromine, a red-brown liquid 

C8.3.2.c

Depth 3

iodine, a grey-black solid

C8.4.1.a

Depth 3

have high densities 

C8.4.1.b

Depth 3

have high melting points

C8.4.1.c

Depth 3

form coloured compounds

C8.4.1.d

Depth 3

often act as catalysts as elements and in compounds

C9.1.1.a

Depth 3

thermal conductivity 

C9.1.1.b

Depth 3

electrical conductivity

C9.1.1.c

Depth 3

malleability and ductility 

C9.1.1.d

Depth 3

melting points and boiling points

C9.1.2.a

Depth 3

dilute acids

C9.1.2.b

Depth 3

cold water and steam

C9.2.1.a

Depth 3

aluminium in the manufacture of aircraft because of its low density

C9.2.1.b

Depth 3

aluminium in the manufacture of overhead electrical cables because of its low density and good electrical conductivity 

C9.2.1.c

Depth 3

aluminium in food containers because of its resistance to corrosion

C9.2.1.d

Depth 3

copper in electrical wiring because of its good electrical conductivity

C9.3.1.a

Depth 3

brass as a mixture of copper and zinc 

C9.3.1.b

Depth 3

stainless steel as a mixture of iron and other elements such as chromium, nickel and carbon

C9.4.2.a

Depth 3

potassium, sodium and calcium with cold water

C9.4.2.b

Depth 3

magnesium with steam 

C9.4.2.c

Depth 3

magnesium, zinc, iron, copper, silver and gold with dilute hydrochloric acid and explain these reactions in terms of the position of the metals in the reactivity series

C9.6.4S.a

Depth 3

the burning of carbon (coke) to provide heat and produce carbon dioxide C + O2 → CO2

C9.6.4S.b

Depth 3

the reduction of carbon dioxide to carbon monoxide С + СО2 → 2CO

C9.6.4S.c

Depth 3

the reduction of iron(III) oxide by carbon monoxide Fe2O3 + 3CO → 2Fe + 3CO2

C9.6.4S.d

Depth 3

the thermal decomposition of calcium carbonate/ limestone to produce calcium oxide CaCO3 → CaO + CO2

C9.6.4S.e

Depth 3

the formation of slag CaO + SiO2 → CaSiO3

C10.1.4.a

Depth 3

sedimentation and filtration to remove solids

C10.1.4.b

Depth 3

use of carbon to remove tastes and odours

C10.1.4.c

Depth 3

chlorination to kill microbes (pathogens)

C10.2.2.a

Depth 3

carbon dioxide from the complete combustion of carbon-containing fuels 

C10.2.2.b

Depth 3

carbon monoxide and particulates from the incomplete combustion of carbon containing fuels 

C10.2.2.c

Depth 3

methane from the decomposition of vegetation and waste gases from digestion in animals (d) oxides of nitrogen from car engines

C10.2.2.d

Depth 3

sulfur dioxide from the combustion of fossil fuels which contain sulfur compounds

C10.2.3.a

Depth 3

carbon dioxide: higher levels of carbon dioxide leading to increased global warming, which leads to climate change 

C10.2.3.b

Depth 3

carbon monoxide: toxic gas

C10.2.3.c

Depth 3

particulates: increased risk of respiratory problems and cancer 

C10.2.3.d

Depth 3

methane: higher levels of methane leading to increased global warming, which leads to climate change

C10.2.3.e

Depth 3

oxides of nitrogen: acid rain and respiratory problems 

C10.2.3.f

Depth 3

sulfur dioxide: acid rain

C10.2.4.a

Depth 3

planting trees 

C10.2.4.b

Depth 3

reduction in livestock farming 

C10.2.4.c

Depth 3

decreasing use of fossil fuels 

C10.2.4.d

Depth 3

increasing use of hydrogen and renewable energy, e.g. wind, solar

C10.2.6S.a

Depth 3

the absorption, reflection and emission of thermal energy 

C10.2.6S.b

Depth 3

reducing thermal energy loss to space

C11.1.5S.a

Depth 3

having the same general formula (recall of specific general formulas is not required) 

C11.1.5S.b

Depth 3

displaying a trend in physical properties

C11.2.1.a

Depth 3

methane and ethane 

C11.2.1.b

Depth 3

ethene

C11.2.1.c

Depth 3

ethanol

C11.2.3S.a

Depth 3

alkanes

C11.2.3S.b

Depth 3

alkenes, including but-1-ene and but-2-ene (not cis/trans) containing up to four carbon atoms per molecule

C11.3.6.a

Depth 3

refinery gas fraction for gas used in heating and cooking 

C11.3.6.b

Depth 3

gasoline / petrol fraction for fuel used in cars

C11.3.6.c

Depth 3

naphtha fraction as a chemical feedstock 

C11.3.6.d

Depth 3

diesel oil / gas oil for fuel used in diesel engines 

C11.3.6.e

Depth 3

bitumen for making roads

C11.3.7S.a

Depth 3

decreasing chain length 

C11.3.7S.b

Depth 3

lower boiling points

C11.5.4S.a

Depth 3

bromine

C11.5.4S.b

Depth 3

hydrogen in the presence of a nickel catalyst 

C11.5.4S.c

Depth 3

steam in the presence of an acid catalyst

C11.6.2.a

Depth 3

a solvent

C11.6.2.b

Depth 3

a fuel

C12.1.1.a

Depth 3

stop-watches

C12.1.1.b

Depth 3

thermometers

C12.1.1.c

Depth 3

balances

C12.1.1.d

Depth 3

burettes

C12.1.1.e

Depth 3

volumetric pipettes 

C12.1.1.f

Depth 3

measuring cylinders

C12.1.1.g

Depth 3

gas syringes

C12.1.2.a

Depth 3

solvent as a substance that dissolves a solute

C12.1.2.b

Depth 3

solute as a substance that is dissolved in a solvent

C12.1.2.c

Depth 3

solution as a mixture of one or more solutes dissolved in a solvent

C12.1.2.d

Depth 3

saturated solution as a solution containing the maximum concentration of a solute dissolved in the solvent at a specified temperature

C12.1.2.e

Depth 3

residue as a solid substance that remains after evaporation, distillation, filtration or any similar process

C12.1.2.f

Depth 3

filtrate as a liquid or solution that has passed through a filter

C12.2.1.a

Depth 3

burette

C12.2.1.b

Depth 3

volumetric pipette 

C12.2.1.c

Depth 3

suitable indicator

C12.3.2.a

Depth 3

unknown substances by comparison with known substances

C12.3.2.b

Depth 3

pure and impure substances

C12.4.1.a

Depth 3

a suitable solvent

C12.4.1.b

Depth 3

filtration

C12.4.1.c

Depth 3

crystallisation

C12.4.1.d

Depth 3

simple distillation

C12.4.1.e

Depth 3

fractional distillation

C12.5.1.a

Depth 3

carbonate, CO3²⁻ by reaction with dilute acid and then testing for carbon dioxide gas

C12.5.1.b

Depth 3

chloride, C⁻, bromide, Br⁻, and iodide, I⁻, by acidifying with dilute nitric acid then adding aqueous silver nitrate

C12.5.1.c

Depth 3

nitrate, NO3⁻ , reduction with aluminium foil and aqueous sodium hydroxide and then testing for ammonia gas

C12.5.1.d

Depth 3

sulfate, SO4²⁻ by acidifying with dilute nitric acid and then adding aqueous barium nitrate

C12.5.2.a

Depth 3

ammonium, NH4⁺

C12.5.2.b

Depth 3

calcium, Ca²⁺

C12.5.2.c

Depth 3

copper(II), Cu²⁺

C12.5.2.d

Depth 3

iron(LI), Fe²⁺

C12.5.2.e

Depth 3

iron(III), Fe³⁺

C12.5.2.f

Depth 3

zinc, Zn²⁺ (formulas of complex ions are not required)

C12.5.3.a

Depth 3

ammonia, NH3, using damp red litmus paper

C12.5.3.b

Depth 3

carbon dioxide, CO2, using limewater 

C12.5.3.c

Depth 3

chlorine, Cl2, using damp litmus paper 

C12.5.3.d

Depth 3

hydrogen, H2, using a lighted splint 

C12.5.3.e

Depth 3

oxygen, O2, using a glowing splint

C12.5.4.a

Depth 3

lithium, Li⁺

C12.5.4.b

Depth 3

sodium, Na⁺

C12.5.4.c

Depth 3

potassium, K⁺ 

C12.5.4.d

Depth 3

copper(II), Cu²⁺

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Source document
Science 0654 (2025-)
License
CC BY 4.0 US