Organic Chemistry
ICSE Class 10 · Chemistry · Chapter 12
What this chapter covers
- Unique nature of the carbon atom
- Single, double and triple bonds, chains and rings
- Structure and isomerism
- Homologous series
- Simple nomenclature
- Alkanes: methane and ethane
- Alkenes: ethene
- Alkynes: ethyne
- Uses of methane, ethane, ethene and ethyne
- Ethanol
- Acetic acid
Key definitions
Organic chemistry is the branch of chemistry that studies the compounds of carbon, mainly the hydrocarbons and the compounds derived from them.
An organic compound is a compound in which carbon atoms are joined covalently to hydrogen and often to other atoms such as oxygen, nitrogen or the halogens.
Tetravalency is the property of the carbon atom of forming four covalent bonds, because it has four valence electrons that it shares with other atoms.
Catenation is the property of an element by which its atoms link with one another through covalent bonds to form long chains, branched chains or rings.
A single covalent bond is a bond formed by the sharing of one pair of electrons between two atoms, shown by a single line, as in C-C.
A double covalent bond is a bond formed by the sharing of two pairs of electrons between two atoms, shown by two lines, as in C=C.
A triple covalent bond is a bond formed by the sharing of three pairs of electrons between two atoms, shown by three lines, as in CequivC.
A saturated hydrocarbon is a hydrocarbon in which all the carbon–carbon bonds are single bonds, so that every carbon atom holds the largest possible number of hydrogen atoms.
An unsaturated hydrocarbon is a hydrocarbon that contains at least one carbon–carbon double or triple bond, so that it can take up more hydrogen or halogen atoms by addition.
A hydrocarbon is a compound made of carbon and hydrogen only.
A cyclic compound is a compound in which the carbon atoms are joined end to end to form a closed ring.
A structural formula is a formula that shows how the atoms in a molecule are joined to one another, with a line for each covalent bond.
Key points
- Carbon forms millions of compounds because of tetravalency (four covalent bonds) and catenation (self-linking into chains and rings).
- Carbon atoms join by single, double or triple bonds and form straight chains, branched chains or rings such as benzene, C6H6.
- Isomers have the same molecular formula but different structures; chain isomers differ in the carbon skeleton, position isomers in where the multiple bond or functional group sits.
- A homologous series has one general formula, members differing by CH2, similar chemical properties and gradually changing physical properties.
- Alkanes CnH2n+2, alkenes CnH2n, alkynes CnH2n-2.
- IUPAC names use the longest chain containing the functional group and the smallest number for that group.
- Methane and ethane are made by heating sodium ethanoate or sodium propanoate with soda lime, or by reducing iodomethane or bromoethane.
- Alkanes burn completely to carbon dioxide and water, incompletely to carbon monoxide or carbon, and react with chlorine by substitution in diffused sunlight.
- Methane is a powerful greenhouse gas from paddy fields, cattle, landfills and gas leaks.
- Ethene is made by dehydrohalogenation of bromoethane or dehydration of ethanol at 170 \circC; ethyne from calcium carbide and water or from 1,2-dibromoethane and alcoholic potassium hydroxide.
- Alkenes and alkynes undergo addition of hydrogen (nickel catalyst) and of chlorine, bromine and iodine; decolourising bromine is a test for unsaturation.
- Ethanol is made by hydrolysis of bromoethane, boils at about 78 \circC, mixes with water, burns cleanly, reacts with sodium, forms esters and is dehydrated to ethene.
- Denatured and methylated spirit are ethanol made unfit to drink; spurious alcohol contains poisonous methanol.
- Acetic acid, CH3COOH, smells of vinegar, freezes into glacial acetic acid, turns blue litmus red, is neutralised by alkalis and forms esters with alcohols.
Questions answered
Define catenation, and give two reasons why carbon shows it more than any other element.
Why does carbon form covalent bonds and not ionic ones?
Write the general formulae of alkanes, alkenes and alkynes, and give the molecular formula of the member of each with four carbon atoms.
State three characteristics of a homologous series.
Draw the condensed structural formulae of the two chain isomers of butane and name them.
Name the type of isomerism shown by but-1-ene and but-2-ene, and give a reason.
Give the IUPAC names of: (a) acetaldehyde, (b) acetone, (c) methyl chloride, (d) ethyl acetate, (e) dimethyl ether.
Write balanced equations for the preparation of methane from sodium ethanoate and of ethane from bromoethane.
Past board exam questions
ICSE 2027 sample paper · 1 mark
Identify the organic compound(s) with the molecular formula C₃H₈O. 1. propanol 2. propanal 3. propanoic acid
- Only 1
- Only 2
- Both 2 and 3
- Both 1 and 2
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ICSE 2027 sample paper · 5 marks
(a) Give the IUPAC name of the following organic compounds: 1. HO–C(=O)–CH₂–CH₂–CH₃ (the carbon bonded to OH carries a double-bonded O) 2. H–C(H)(H)–C(H)(CH₃)–C(H)(H)–C(H)(CH₃)–H (a four-carbon chain drawn left to right: the 1st carbon carries three H; the 2nd carries one H above and a CH₃ below; the 3rd carries two H; the 4th carries one H above, a CH₃ below and an H on the right) (b) Draw the structural diagram for the following compounds: 1. diethyl ether 2. isopentane 3. propanone
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ICSE 2027 sample paper · 2 marks
What is the ratio of methane to the acidic gaseous product obtained when methane undergoes complete combustion? Give a balanced equation for the above reaction.
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ICSE 2027 sample paper · 3 marks
Give balanced equations for each of the following: (a) Action of warm water on calcium carbide. (b) Oxidation of sulphur with conc. nitric acid. (c) Laboratory preparation of ethane by using sodium propionate and soda lime.
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ICSE 2027 sample paper · 4 marks
The structures of five organic compounds, C, D, E, F and G are shown. - C: CH₃–CH=CH₂ - D: CH₃–CH₂–CH₂–OH - E: CH₃–CH₂–CH₂–CH₃ - F: CH₂Br–CH₂Br - G: CH₂=CH₂ (Each was printed as a full structural formula with every bond shown.) Answer the following questions about these compounds. (Each compound may be used once, more than once or not at all.) State which compound, C, D, E, F or G: (a) on halogenation will form F. (b) is an alcohol. (c) is an isomer of 2-methyl propane. (d) is in the same homologous series as ethene.
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ICSE 2026 sample paper · 1 mark
The structures of four hydrocarbons are shown below: 1. CH₃–CH(CH₃)–CH₃ (a central C bonded to H, to CH₃ on the left, and to CH₃ above and below) 2. (CH₃)₂C=CH₂ (a central C with CH₃ above, CH₃ below, and =CH₂ to the right) 3. CH₃–CH₂–CH=CH₂ 4. CH₃–C(CH₃)=CH₂ (CH₃ on the left, CH₃ above, =CH₂ to the right) How many isomers of butene are shown in the above structures?
- 1
- 2
- 3
- 4
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ICSE 2026 board paper · 1 mark
Identify the equation that shows the reaction of ethane with chlorine in the presence of ultraviolet light.
- C₂H₆ + Cl₂ ⟶ C₂H₆Cl₂
- C₂H₆ + Cl₂ ⟶ C₂H₄Cl₂ + H₂
- C₂H₆ + Cl₂ ⟶ C₂H₅Cl + HCl
- C₂H₆ + Cl₂ ⟶ 2CH₃Cl
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ICSE 2026 board paper · 1 mark
A hydrocarbon X undergoes the reaction under suitable conditions as shown below: X (H₃C–CH₂–CH₂–CH₃) ⟶ Y (H₂C=CH–CH₃) + Z (CH₄) (X: four carbon atoms in a chain joined by single bonds, each carbon carrying hydrogens; Y: H₂C=CH–CH₃, a carbon–carbon double bond between the first two carbons; Z: one carbon with four hydrogens.) Which compound(s) is/are unsaturated?
- X only
- Y only
- X and Z
- Y and Z