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  2. Haloalkane - Wikipedia

    en.wikipedia.org/wiki/Haloalkane

    In primary (1°) haloalkanes, the carbon that carries the halogen atom is only attached to one other alkyl group. An example is chloroethane (CH 3 CH 2 Cl). In secondary (2°) haloalkanes, the carbon that carries the halogen atom has two C–C bonds. In tertiary (3°) haloalkanes, the carbon that carries the halogen atom has three C–C bonds.

  3. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    An example of a reaction taking place with an S N 1 reaction mechanism is the hydrolysis of tert-butyl bromide forming tert-butanol: This S N 1 reaction takes place in three steps: Formation of a tert-butyl carbocation by separation of a leaving group (a bromide anion) from the carbon atom: this step is slow. [5] Recombination of carbocation ...

  4. Lucas' reagent - Wikipedia

    en.wikipedia.org/wiki/Lucas'_reagent

    Primary alcohols do not react appreciably with Lucas reagent at room temperature. [3] Hence, the time taken for turbidity to appear is a measure of the reactivity of the class of alcohol, and this time difference is used to differentiate among the three classes of alcohols:

  5. Williamson ether synthesis - Wikipedia

    en.wikipedia.org/wiki/Williamson_ether_synthesis

    The alkoxide (or aryloxide) may be primary and secondary. Tertiary alkoxides tend to give elimination reaction because of steric hindrance. The alkylating agent, on the other hand is most preferably primary. Secondary alkylating agents also react, but tertiary ones are usually too prone to side reactions to be of practical use.

  6. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    For example, cyclobutane and methylcyclopropane are isomers of each other (C 4 H 8), but are not isomers of butane (C 4 H 10). Branched alkanes are more thermodynamically stable than their linear (or less branched) isomers. For example, the highly branched 2,2,3,3-tetramethylbutane is about 1.9 kcal/mol more stable than its linear isomer, n ...

  7. Free-radical halogenation - Wikipedia

    en.wikipedia.org/wiki/Free-radical_halogenation

    tertiary (5) > secondary (3.8) > primary (1). Thus any single chlorination step slightly favors substitution at the carbon already most substituted. The rates are generally constant across reactions and predict product distributions with relatively high accuracy. [3] [4] For example, 2-methyl butane ((CH 3) 2 CHCH 2 CH 3) exhibits the following ...

  8. 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 ...

  9. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    Methyl and primary substrates react the fastest, followed by secondary substrates. Tertiary substrates do not react via the S N 2 pathway, as the greater steric hindrance between the nucleophile and nearby groups of the substrate will leave the S N 1 reaction to occur first. Substrates with adjacent pi C=C systems can favor both S N 1 and S N 2 ...