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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. 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 ...

  4. Disulfide - Wikipedia

    en.wikipedia.org/wiki/Disulfide

    Rotation about the SS axis is subject to a low barrier. Disulfides show a distinct preference for dihedral angles approaching 90°. When the angle approaches 0° or 180°, then the disulfide is a significantly better oxidant. Disulfides where the two R groups are the same are called symmetric, examples being diphenyl disulfide and dimethyl ...

  5. Alkylation - Wikipedia

    en.wikipedia.org/wiki/Alkylation

    Alkylation is a chemical reaction that entails transfer of an alkyl group. The alkyl group may be transferred as an alkyl carbocation, a free radical, a carbanion, or a carbene (or their equivalents). [1] Alkylating agents are reagents for effecting alkylation. Alkyl groups can also be removed in a process known as dealkylation.

  6. Thiol - Wikipedia

    en.wikipedia.org/wiki/Thiol

    Thiol with a blue highlighted sulfhydryl group.. In organic chemistry, a thiol (/ ˈ θ aɪ ɒ l /; [1] from Ancient Greek θεῖον (theion) 'sulfur' [2]), or thiol derivative, is any organosulfur compound of the form R−SH, where R represents an alkyl or other organic substituent.

  7. Organic sulfide - Wikipedia

    en.wikipedia.org/wiki/Organic_sulfide

    Trialkysulfonium salts react with nucleophiles with a dialkyl sulfide as a leaving group: Nu − + R 3 S + → Nu-R + R 2 SR 1. This reaction is exploited in biological systems as a means of transferring an alkyl group. For example, S-adenosylmethionine acts as a methylating agent in biological S N 2 reactions.

  8. Acyl group - Wikipedia

    en.wikipedia.org/wiki/Acyl_group

    The hydrocarbyl group names that end in -yl are not acyl groups, but alkyl groups derived from alkanes (methyl, ethyl, propyl, butyl), alkenyl groups derived from alkenes (propenyl, butenyl), or aryl groups .

  9. Alkylidene group - Wikipedia

    en.wikipedia.org/wiki/Alkylidene_group

    In organic chemistry, alkylidene is a general term for divalent functional groups of the form R 2 C=, where each R is an alkane or hydrogen. [1] They can be considered the functional group corresponding to mono- or disubstituted divalent carbenes (known as alkylidenes), [2] or as the result of removing two hydrogen atoms from the same carbon atom in an alkane.