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  2. 2-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/2-Bromobutane

    2-Bromobutane is an isomer of 1-bromobutane. Both compounds share the molecular formula C 4 H 9 Br. 2-Bromobutane is also known as sec-butyl bromide or methylethylbromomethane. Because it contains bromine, a halogen, it is part of a larger class of compounds known as alkyl halides. It is a colorless liquid with a pleasant odor.

  3. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    An example of a reaction proceeding in a S N 1 fashion is the synthesis of 2,5-dichloro-2,5-dimethylhexane from the corresponding diol with concentrated hydrochloric acid: [8] As the alpha and beta substitutions increase with respect to leaving groups, the reaction is diverted from S N 2 to S N 1.

  4. Solvolysis - Wikipedia

    en.wikipedia.org/wiki/Solvolysis

    Ammonolysis refers to solvolysis by ammonia, but can also describe nucleophilic attack by ammonia more generally. Ammonia boils at −33 °C, and, as such, is rarely used as a solvent in its pure form. It is, however, readily miscible with water, and is commonly used in the form of a saturated aqueous solution. For this reason, ammonolysis may ...

  5. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    In S N 2 reactions, there are a few conditions that affect the rate of the reaction. First of all, the 2 in S N 2 implies that there are two concentrations of substances that affect the rate of reaction: substrate (Sub) and nucleophile. The rate equation for this reaction would be Rate=k[Sub][Nuc].

  6. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    The stability of a carbocation (C +) depends on how many other carbon atoms are bonded to it. This results in S N 1 reactions usually occurring on atoms with at least two carbons bonded to them. [2] A more detailed explanation of this can be found in the main SN1 reaction page. S N 2 reaction mechanism. The S N 2 mechanism has just one step ...

  7. C4H9Br - Wikipedia

    en.wikipedia.org/wiki/C4H9Br

    The molecular formula C 4 H 9 Br, (molar mass: 137.02 g/mol, exact mass: 135.9888 u) may refer to: 1-Bromobutane; 2-Bromobutane; tert-Butyl bromide;

  8. 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.

  9. Bromobutane - Wikipedia

    en.wikipedia.org/wiki/Bromobutane

    Bromobutane (molecular formula: C 4 H 9 Br, molar mass: 137.02 g/mol) may refer to either of two chemical compounds: 1-Bromobutane ( n -butyl bromide) 2-Bromobutane ( sec -butyl bromide or methylethylbromomethane)