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  2. Alcohol fuel - Wikipedia

    en.wikipedia.org/wiki/Alcohol_fuel

    The reaction mechanism is 3 EtOH + Al -> Al(OEt) 3 + 3 ⁄ 2 H 2 at lower-mid blends. When enough water is present in the fuel, aluminum will react preferably with water to produce Al 2 O 3, repairing the protective aluminum oxide layer. The aluminum alkoxide does not make a tight oxide layer; water is essential to repair the holes in the oxide ...

  3. Ethanol - Wikipedia

    en.wikipedia.org/wiki/Ethanol

    This reaction, which is conducted on large scale industrially, requires the removal of the water from the reaction mixture as it is formed. Esters react in the presence of an acid or base to give back the alcohol and a salt. This reaction is known as saponification because it is used in the preparation of soap. Ethanol can also form esters with ...

  4. Sodium ethoxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_ethoxide

    It is easily prepared in the laboratory by treating sodium metal with absolute ethanol: [3] 2 CH 3 CH 2 OH + 2 Na → 2 CH 3 CH 2 ONa + H 2. The reaction of sodium hydroxide with anhydrous ethanol suffers from incomplete conversion to the ethoxide, but can still produce dry NaOEt by precipitation using acetone, [4] or by drying using additional ...

  5. Ethanol fuel - Wikipedia

    en.wikipedia.org/wiki/Ethanol_fuel

    During combustion, ethanol reacts with oxygen to produce carbon dioxide, water, and heat: C 2 H 5 OH + 3 O 2 → 2 CO 2 + 3 H 2 O + heat. Starch and cellulose molecules are strings of glucose molecules. It is also possible to generate ethanol out of cellulosic materials.

  6. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  7. Standard Gibbs free energy of formation - Wikipedia

    en.wikipedia.org/wiki/Standard_Gibbs_free_energy...

    The standard Gibbs free energy of formation (G f °) of a compound is the change of Gibbs free energy that accompanies the formation of 1 mole of a substance in its standard state from its constituent elements in their standard states (the most stable form of the element at 1 bar of pressure and the specified temperature, usually 298.15 K or 25 °C).

  8. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    The term alcohol originally referred to the primary alcohol ethanol (ethyl alcohol), which is used as a drug and is the main alcohol present in alcoholic drinks. The suffix -ol appears in the International Union of Pure and Applied Chemistry (IUPAC) chemical name of all substances where the hydroxyl group is the functional group with the ...

  9. Ethane - Wikipedia

    en.wikipedia.org/wiki/Ethane

    The combustion of ethane releases 1559.7 kJ/mol, or 51.9 kJ/g, of heat, and produces carbon dioxide and water according to the chemical equation: 2 C 2 H 6 + 7 O 2 → 4 CO 2 + 6 H 2 O + 3120 kJ. Combustion may also occur without an excess of oxygen, yielding carbon monoxide, acetaldehyde, methane, methanol, and ethanol.