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  2. 1-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/1-Bromobutane

    As a primary haloalkane, it is prone to S N 2 type reactions. It is commonly used as an alkylating agent. When combined with magnesium metal in dry ether, it gives the corresponding Grignard reagent. Such reagents are used to attach butyl groups to various substrates. 1-Bromobutane is the precursor to n-butyllithium: [4]

  3. Haloalkane - Wikipedia

    en.wikipedia.org/wiki/Haloalkane

    Haloalkanes behave as the R + synthon, and readily react with nucleophiles. [citation needed] Hydrolysis, a reaction in which water breaks a bond, is a good example of the nucleophilic nature of haloalkanes. The polar bond attracts a hydroxide ion, OH − (NaOH (aq) being a common source of this ion).

  4. 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.

  5. Arrow pushing - Wikipedia

    en.wikipedia.org/wiki/Arrow_pushing

    Arrow pushing or electron pushing is a technique used to describe the progression of organic chemistry reaction mechanisms. [1] It was first developed by Sir Robert Robinson.In using arrow pushing, "curved arrows" or "curly arrows" are drawn on the structural formulae of reactants in a chemical equation to show the reaction mechanism.

  6. Hydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrohalogenation

    A hydrohalogenation reaction is the electrophilic addition of hydrogen halides like hydrogen chloride or hydrogen bromide to alkenes to yield the corresponding haloalkanes. [ 1 ] [ 2 ] [ 3 ] If the two carbon atoms at the double bond are linked to a different number of hydrogen atoms, the halogen is found preferentially at the carbon with fewer ...

  7. 1,1,1,2-Tetrafluoroethane - Wikipedia

    en.wikipedia.org/wiki/1,1,1,2-Tetrafluoroethane

    1,1,1,2-Tetrafluoroethane (also known as norflurane (), R-134a, Klea 134a, Freon 134a, Forane 134a, Genetron 134a, Green Gas, Florasol 134a, Suva 134a, HFA-134a, or HFC-134a) is a hydrofluorocarbon (HFC) and haloalkane refrigerant with thermodynamic properties similar to R-12 (dichlorodifluoromethane) but with insignificant ozone depletion potential and a lower 100-year global warming ...

  8. Reaction coordinate - Wikipedia

    en.wikipedia.org/wiki/Reaction_coordinate

    Diagram of a catalytic reaction, showing the energy level as a function of the reaction coordinate. For a catalyzed reaction, the activation energy is lower. In chemistry , a reaction coordinate [ 1 ] is an abstract one-dimensional coordinate chosen to represent progress along a reaction pathway.

  9. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    A diagram showing the bond dipole moments of boron trifluoride. δ- shows an increase in negative charge and δ+ shows an increase in positive charge. Note that the dipole moments drawn in this diagram represent the shift of the valence electrons as the origin of the charge, which is opposite the direction of the actual electric dipole moment.