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Q.Describe two methods of preparation of ethane. Give any three reactions of ethane.

Telangana TsbieTelangana Board of Intermediate Education (Intermediate 1st Year) 2022Subjective· 8mImportance★★★★★
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Ethane (C2H6), the simplest alkane after methane, is commonly prepared by hydrogenating unsaturated hydrocarbons or via the Wurtz reaction, and undergoes typical alkane reactions — combustion, free-radical halogenation, and thermal cracking.

Methods of preparation of ethane

  1. Catalytic hydrogenation of unsaturated hydrocarbons:

    Ethene (or ethyne) is treated with hydrogen gas in the presence of a finely divided metal catalyst (Ni, Pt, or Pd), which adsorbs H2 and the alkene/alkyne onto its surface, allowing addition of hydrogen across the multiple bond:

    CH2=CH2+H2→Ni/Pt/PdCH3−CH3CH_2=CH_2 + H_2 \xrightarrow{Ni/Pt/Pd} CH_3-CH_3

    (Ethyne, CH≡CH, similarly adds 2 molecules of H2 to give ethane.)

  2. Wurtz reaction:

    An alkyl halide is treated with metallic sodium in dry ether. Two alkyl groups couple together, releasing NaX:

    2CH3I+2Na→dry etherCH3−CH3+2NaI2CH_3I + 2Na \xrightarrow{\text{dry ether}} CH_3-CH_3 + 2NaI

    This method works well when both alkyl groups are the same (here, both methyl), directly giving ethane.

Three reactions of ethane

  1. Combustion: Like other alkanes, ethane burns completely in excess oxygen/air to give carbon dioxide, water, and release a large amount of heat (making alkanes useful fuels):

    C2H6+72O2→2CO2+3H2O+heatC_2H_6 + \dfrac{7}{2}O_2 \rightarrow 2CO_2 + 3H_2O + \text{heat}

  2. Halogenation (free-radical substitution): In the presence of sunlight or heat, ethane reacts with halogens (e.g. Cl2) via a free-radical chain mechanism, substituting hydrogen atoms one at a time:

    C2H6+Cl2→hνC2H5Cl+HClC_2H_6 + Cl_2 \xrightarrow{h\nu} C_2H_5Cl + HCl …

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