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Welcome to GCSE Edexcel Science revision.

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Unit S C 23: Alcohols and carboxylic acids.

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Alcohols contain the O H functional group attached to carbon, called a hydroxyl group.

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A functional group is the part of a molecule responsible for its characteristic reactions.

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The alcohol’s covalently bonded O H is different from a free hydroxide ion, O H, charge minus, in an alkali.

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The first four straight-chain primary alcohols here are methanol C H 3 O H, ethanol C H 3 C H 2 O H, propan-1-ol C H 3 C H 2 C H 2 O H and butan-1-ol C H 3 C H 2 C H 2 C H 2 O H.

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Show all atoms and bonds when asked for displayed formulae.

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The O to H group is bonded to the final carbon; all covalent bonds are shown.

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These members belong to a homologous series: they share the O H group, have similar reactions and differ successively by C H 2.

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Their boiling points generally rise with chain length.

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Alcohols burn in oxygen.

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Complete combustion produces carbon dioxide and water; ethanol obeys C 2 H 5 O H plus 3 O 2 produces 2 C O 2 plus 3 H 2 O.

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Insufficient oxygen can produce carbon monoxide or soot.

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Alcohols can be dehydrated to form alkenes by removing water.

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Ethanol forms ethene: C 2 H 5 O H produces C 2 H 4 plus H 2 O.

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Dehydration is removal of the elements of water, not simply evaporation of solvent.

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The carbon count is unchanged; an alkene double bond forms.

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Ethanol can be oxidised to ethanoic acid.

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Other suitable primary alcohols can similarly form the carboxylic acid with the same carbon count; the required oxidising reagents are beyond the recall scope here.

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Methanol is toxic, and alcohols are flammable.

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Do not infer that every alcohol has the uses or safety profile of ethanol.

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Compare ethanol, propanol, butanol and pentanol by burning them in spirit burners beneath a known mass of water.

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Measure initial and final water temperatures and weigh each burner before and after heating.

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Keep the separation between flame and water container constant.

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Keep the water mass, burner-to-container distance, apparatus, starting temperature and mixing method consistent.

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Stir the water for a representative temperature and use a lid or draught shield where appropriate.

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Water energy gain equals mass times specific heat capacity times temperature rise.

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With water mass in grams and c equals 4.2 joules per gram per degree Celsius, the result is joules; energy per gram burned equals energy gained divided by fuel mass burned.

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For comparison per mole, calculate fuel moles from mass divided by relative formula mass, then divide measured energy by the amount burned.

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Per-gram and per-mole comparisons answer different questions.

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Heat loss to the surroundings and container, incomplete combustion, evaporation of fuel and changes in flame conditions reduce accuracy.

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A simple apparatus usually captures less than the true combustion energy.

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Use repeats and means, identify anomalies and avoid concluding that a larger temperature rise means a better fuel unless the amounts burned and conditions are comparable.

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Wear eye protection, keep spare fuel away from flames, extinguish burners safely with their caps and allow hot apparatus to cool.

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Never refill a burning or hot spirit burner.

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Carboxylic acids contain the C O O H functional group: a carbon with a C double bonded to O bond and an O H group.

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The first four are methanoic acid H C O O H, ethanoic acid C H 3 C O O H, propanoic acid C H 3 C H 2 C O O H and butanoic acid C H 3 C H 2 C H 2 C O O H.

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The carboxyl carbon has a C double bonded to O bond and a C to O, H group.

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It counts in the chain length.

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The carbon in the C O O H group counts towards the molecule’s total carbon number.

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Ethanoic acid has two carbons, while methanoic acid has one; do not omit the functional-group carbon.

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Solutions of carboxylic acids show acidic properties: they turn blue litmus red and react with suitable metals, bases, alkalis and carbonates.

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Many simple carboxylic acids are weak acids because only some molecules ionise in water.

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A carboxylic acid and an alkali form a salt and water; ethanoic acid with sodium hydroxide gives sodium ethanoate and water.

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The salt name changes the acid ending to -oate.

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With a carbonate, a carboxylic acid forms a salt, carbon dioxide and water.

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Confirm carbon dioxide by its ability to turn limewater cloudy; bubbles alone do not identify a gas.

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With a suitable reactive metal, a carboxylic acid forms a salt and hydrogen.

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Reaction rates depend on the acid and metal; do not claim all metals react equally.

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Members of the carboxylic-acid series have similar reactions because they share C O O H.

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Use the same pattern to predict a reaction of another member.

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That completes Alcohols and carboxylic acids.

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Revisit the notes and test yourself on the revision website.
