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  2. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    Competition experiment between SN2 and E2. With ethyl bromide, the reaction product is predominantly the substitution product. As steric hindrance around the electrophilic center increases, as with isobutyl bromide, substitution is disfavored and elimination is the predominant reaction. Other factors favoring elimination are the strength of the ...

  3. Concerted reaction - Wikipedia

    en.wikipedia.org/wiki/Concerted_reaction

    The reaction does not have any intermediate steps, only a transition state. This means that all the bond making and bond breaking takes place in a single step. In order for the reaction to occur both molecules must be situated correctly.

  4. Energy profile (chemistry) - Wikipedia

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

    The relative stability of reactant and product does not define the feasibility of any reaction all by itself. For any reaction to proceed, the starting material must have enough energy to cross over an energy barrier. This energy barrier is known as activation energy (∆G ≠) and the rate of reaction is dependent on the height of this barrier ...

  5. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    It is also due to this carbocation intermediate that the product does not have to have inversion. The nucleophile can attack from the top or the bottom and therefore create a racemic product. It is important to use a protic solvent, water and alcohols, since an aprotic solvent could attack the intermediate and cause unwanted product.

  6. Transition state - Wikipedia

    en.wikipedia.org/wiki/Transition_state

    The concept of a transition state has been important in many theories of the rates at which chemical reactions occur. This started with the transition state theory (also referred to as the activated complex theory), which was first developed around 1935 by Eyring, Evans and Polanyi, and introduced basic concepts in chemical kinetics that are still used today.

  7. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    For S N 1 reactions the solvent's ability to stabilize the intermediate carbocation is of direct importance to its viability as a suitable solvent. The ability of polar solvents to increase the rate of S N 1 reactions is a result of the polar solvent's solvating the reactant intermediate species, i.e., the carbocation, thereby decreasing the ...

  8. Why Trump’s tariff plans could lead to higher interest rates

    www.aol.com/finance/why-trump-tariff-plans-could...

    President-elect Donald Trump’s promise to impose stiff tariffs against America’s three biggest trading partners is widely expected to push prices higher, which would set the stage for the ...

  9. Hammond's postulate - Wikipedia

    en.wikipedia.org/wiki/Hammond's_postulate

    For example, electrophilic aromatic substitution involves a distinct intermediate and two less well defined states. By measuring the effects of aromatic substituents and applying Hammond's postulate it was concluded that the rate-determining step involves formation of a transition state that should resemble the intermediate complex. [6]