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  2. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    A cycloalkyl group is derived from a cycloalkane by removal of a hydrogen atom from a ring and has the general formula −C n H 2n−1. [2] Typically an alkyl is a part of a larger molecule. In structural formulae, the symbol R is used to designate a generic (unspecified) alkyl group. The smallest alkyl group is methyl, with the formula −CH 3 ...

  3. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    When compounds contain more than one functional group, the order of precedence determines which groups are named with prefix or suffix forms. The table below shows common groups in decreasing order of precedence. The highest-precedence group takes the suffix, with all others taking the prefix form.

  4. Inductive effect - Wikipedia

    en.wikipedia.org/wiki/Inductive_effect

    However, some groups, such as the alkyl group, are less electron-withdrawing than hydrogen and are therefore considered as electron-releasing/ electron-donating groups. This is electron-releasing character and is indicated by the +I effect. In short, alkyl groups tend to give electrons, leading to the induction effect.

  5. Category:Alkyl groups - Wikipedia

    en.wikipedia.org/wiki/Category:Alkyl_groups

    Alkyl groups are saturated hydrocarbons substituents with the general formula C n H 2n+1 Pages in category "Alkyl groups" The following 7 pages are in this category ...

  6. 1,2-Wittig rearrangement - Wikipedia

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

    The alkyl group migrates in the order of thermodynamical stability methyl < primary alkyl < secondary alkyl < tertiary alkyl, this is in line with the radical mechanism. The radical-ketyl pair is short lived and due to a solvent cage effect some isomerizations take place with retention of configuration .

  7. Baker–Nathan effect - Wikipedia

    en.wikipedia.org/wiki/Baker–Nathan_effect

    The observed order in this particular reaction however was methyl > ethyl> isopropyl > tert-butyl. In 1935 Baker and Nathan explained the observed difference in terms of a conjugation effect and in later years after the advent of hyperconjugation (1939) as its predecessor.

  8. Leaving group - Wikipedia

    en.wikipedia.org/wiki/Leaving_group

    In the situation where other variables are held constant (nature of the alkyl electrophile, solvent, etc.), a change in nucleophile can lead to a change in the order of reactivity for leaving groups. In the case below, tosylate is the best leaving group when ethoxide is the nucleophile, but iodide and even bromide become better leaving groups ...

  9. Category:Alkyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Alkyl_compounds

    Alkyl compounds are chemical compounds formally derived from alkanes by replacement of one hydrogen atom with other atoms or functional groups. Alkyl compounds contain alkyl groups , C n H 2 n +1 , and have the general formula C n H 2 n +1 X, where X is any chemical element or group.