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Welcome to GCSE Edexcel Science revision.

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Unit S C 19: Heat energy changes in chemical reactions.

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An exothermic change transfers heat energy from the reacting system to the surroundings, so the surrounding temperature can rise.

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The system loses energy overall.

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An endothermic change takes in heat from surroundings, which can cool.

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The system gains energy overall.

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Temperature observations depend on heat exchange and insulation.

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Common exothermic examples include combustion and many acid, alkali neutralisations and displacement reactions.

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Do not infer every reaction's energy change from its category alone without evidence.

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Dissolving salts in water can release or absorb heat depending on the salt.

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Precipitation reactions can also show measurable temperature changes.

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The same energy transfer can be described from two perspectives: an exothermic system loses heat while surroundings gain it.

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A temperature change in a solution reflects exchange with that solution and apparatus.

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For the reverse of a reaction, the energy change has the opposite sign.

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An exothermic forward reaction has an endothermic reverse reaction.

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For a solution reaction, measure suitable reagent volumes and starting temperatures, mix in an insulated container and record the highest or lowest temperature reached.

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Use a polystyrene cup with a lid where appropriate to reduce heat exchange with the room.

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Support the cup securely in a beaker and use an appropriate thermometer or temperature probe.

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Insulation and a lid reduce exchange with the room; stir and record the extreme temperature.

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Temperature change delta T equals final relevant temperature minus initial temperature.

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A rise gives positive delta T for the measured surroundings; a fall gives negative delta T.

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For a comparison, control reagent amounts and concentrations, initial temperature, container and mixing.

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Repeat runs and use comparable recording intervals.

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Heat loss during an exothermic reaction can make the observed maximum rise too small.

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Heat entering from the room can make an endothermic cooling appear smaller.

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Wear eye protection and follow the specified dilute-reagent method.

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A rise alone does not identify every product, and a small change may be limited by instrument resolution.

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A reaction profile plots energy vertically against reaction progress horizontally.

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Reaction progress is not a time axis.

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Reactants begin at one energy level, the curve reaches a peak, and products end at another.

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The activation energy is the difference from the reactant level to the peak for the forward reaction.

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Activation energy is the minimum energy barrier required for successful reaction.

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Exothermic reactions still need an initial energy input; a fuel does not necessarily ignite spontaneously.

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For an exothermic reaction the product level is below reactants.

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Overall energy change delta H equals energy of products minus energy of reactants is negative.

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Products lower than reactants; activation energy remains positive.

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For an endothermic reaction the product level is above reactants and delta H is positive.

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The activation-energy arrow must still start at the reactant level.

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Products higher than reactants; distinguish overall delta H from the activation barrier.

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A catalyst gives an alternative pathway with a lower peak, reducing activation energy.

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Reactant and product energy levels and overall energy change remain unchanged.

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A catalyst changes the pathway and activation energy, not delta H.

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Forward and reverse activation energies are measured from different starting levels to the relevant peak.

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They are not necessarily equal.

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Breaking chemical bonds requires energy and is endothermic.

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It is incorrect to say breaking a fuel's bonds itself releases energy.

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Forming chemical bonds releases energy and is exothermic.

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Overall reaction energy depends on both bond breaking and bond making.

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An exothermic reaction releases more energy in forming product bonds than it takes in to break reactant bonds.

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An endothermic reaction takes in more than it releases.

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An exothermic result releases more in making bonds than it needs for breaking them.

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Average bond energies are usually given in kilojoules per mole of bonds.

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They are average values, so calculations using them may differ from the actual measured energy change of a reaction (its enthalpy change).

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Count all bonds in every molecule, multiplying by the balanced-equation coefficients.

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A double bond has its given double-bond energy, not necessarily twice a single-bond value.

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Estimated reaction energy change equals total energy needed to break reactant bonds minus total energy released forming product bonds.

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Use the sign to identify endothermic or exothermic.

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For H 2 plus C L 2 produces 2 H C L,

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using H to H 436,

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C L to C L 243 and H to C L 431 kilojoules per mole: break 436 plus 243 equals 679;

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form 2 times 431 equals 862;

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delta H equals 679 minus 862 equals minus 183 kilojoules per mole for the equation as written.

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Equation: H 2 plus C L 2 produces 2 H C L; negative delta H is exothermic.

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For 2 H 2 plus O 2 produces 2 H 2 O,

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using H to H 436,

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O double bonded to O 498 and O to H 463: break 2 times 436 plus 498 equals 1370;

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form 4 times 463 equals 1852;

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delta H equals minus 482 kilojoules per mole for two moles of water as written.

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For C H 4 plus 2 O 2 produces C O 2 plus 2 H 2 O, count four C to H bonds and two O double bonded to O bonds broken; two C double bonded to O bonds and four O to H bonds formed.

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Coefficients are essential.

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If a question asks per mole of one product rather than per balanced reaction, adjust accordingly.

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For the water equation above, per mole of water is minus 241 kilojoules per mole using those average values.

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Show the bond counts and both totals before subtracting.

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A negative answer indicates heat released overall; do not drop a minus sign just because the released energy has a positive magnitude.

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That completes Heat energy changes in chemical reactions.

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Revisit the notes and test yourself on the revision website.
