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  2. Ammonia borane - Wikipedia

    en.wikipedia.org/wiki/Ammonia_borane

    The molecule adopts a structure similar to that of ethane, with which it is isoelectronic. The B−N distance is 1.58(2) Å. The B−H and N−H distances are 1.15 and 0.96 Å, respectively. Its similarity to ethane is tenuous since ammonia borane is a solid and ethane is a gas: their melting points differing by 284 °C.

  3. Boron trifluoride - Wikipedia

    en.wikipedia.org/wiki/Boron_trifluoride

    BF 3 is commonly referred to as "electron deficient," a description that is reinforced by its exothermic reactivity toward Lewis bases. In the boron trihalides, BX 3, the length of the B–X bonds (1.30 Å) is shorter than would be expected for single bonds, [7] and this shortness may indicate stronger B–X π-bonding in the fluoride.

  4. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    [1] [2] [3] Introduced by Gilbert N. Lewis in his 1916 article The Atom and the Molecule, a Lewis structure can be drawn for any covalently bonded molecule, as well as coordination compounds. [4] Lewis structures extend the concept of the electron dot diagram by adding lines between atoms to represent shared pairs in a chemical bond.

  5. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    MO diagram of dihydrogen Bond breaking in MO diagram. The smallest molecule, hydrogen gas exists as dihydrogen (H-H) with a single covalent bond between two hydrogen atoms. As each hydrogen atom has a single 1s atomic orbital for its electron, the bond forms by overlap of these two atomic orbitals. In the figure the two atomic orbitals are ...

  6. Ethenone - Wikipedia

    en.wikipedia.org/wiki/Ethenone

    Ethenone reacts with methanal in the presence of catalysts such as Lewis acids (AlCl 3, ZnCl 2 or BF 3) to give β-propiolactone. [21] The technically most significant use of ethenone is the synthesis of sorbic acid by reaction with 2-butenal (crotonaldehyde) in toluene at about 50 °C in the presence of zinc salts of long-chain carboxylic acids.

  7. Ether - Wikipedia

    en.wikipedia.org/wiki/Ether

    Since phenols are acidic, they readily react with a strong base like sodium hydroxide to form phenoxide ions. The phenoxide ion will then substitute the –X group in the alkyl halide, forming an ether with an aryl group attached to it in a reaction with an S N 2 mechanism. C 6 H 5 OH + OH − → C 6 H 5 –O − + H 2 O C 6 H 5 –O − + R ...

  8. Triple point - Wikipedia

    en.wikipedia.org/wiki/Triple_point

    A typical phase diagram.The solid green line applies to most substances; the dashed green line gives the anomalous behavior of water. In thermodynamics, the triple point of a substance is the temperature and pressure at which the three phases (gas, liquid, and solid) of that substance coexist in thermodynamic equilibrium. [1]

  9. Energy profile (chemistry) - Wikipedia

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

    Figure 6:Reaction Coordinate Diagrams showing reactions with 0, 1 and 2 intermediates: The double-headed arrow shows the first, second and third step in each reaction coordinate diagram. In all three of these reactions the first step is the slow step because the activation energy from the reactants to the transition state is the highest.