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  2. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    In organic chemistry, an alkyl group is an alkane missing one hydrogen. [1] The term alkyl is intentionally unspecific to include many possible substitutions. An acyclic alkyl has the general formula of −CnH2n+1. A cycloalkyl group is derived from a cycloalkane by removal of a hydrogen atom from a ring and has the general formula −CnH2n−1 ...

  3. Inductive effect - Wikipedia

    en.wikipedia.org/wiki/Inductive_effect

    Inductive effect. In Organic chemistry, the inductive effect in a molecule is a local change in the electron density due to electron-withdrawing or electron-donating groups elsewhere in the molecule, resulting in a permanent dipole in a bond. [1] It is present in a σ (sigma) bond, unlike the electromeric effect which is present in a π (pi) bond.

  4. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    List of straight-chain alkanes. The following is a list of straight-chain alkanes, the total number of isomers of each (including branched chains), and their common names, sorted by number of carbon atoms. [1][2] Number of C atoms. Number of isomers [3][4] Number of isomers including stereoisomers [3][5] Molecular Formula. Name of straight chain.

  5. IUPAC nomenclature of organic chemistry - Wikipedia

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

    If the alkyl group is not attached at the end of the chain, the bond position to the ester group is suffixed before "-yl": CH 3 CH 2 CH(CH 3)OOCCH 2 CH 3 may be called butan-2-yl propanoate or butan-2-yl propionate. [citation needed]. The prefix form is "oxycarbonyl-" with the (R') group preceding.

  6. Functional group - Wikipedia

    en.wikipedia.org/wiki/Functional_group

    A functional group is a group of atoms in a molecule with distinctive chemical properties, regardless of the other atoms in the molecule. The atoms in a functional group are linked to each other and to the rest of the molecule by covalent bonds. For repeating units of polymers, functional groups attach to their nonpolar core of carbon atoms and ...

  7. Ethoxylation - Wikipedia

    en.wikipedia.org/wiki/Ethoxylation

    Ethoxylation. In organic chemistry, ethoxylation is a chemical reaction in which ethylene oxide (C2H4O) adds to a substrate. It is the most widely practiced alkoxylation, which involves the addition of epoxides to substrates. In the usual application, alcohols and phenols are converted into R (OC2H4)nOH, where n ranges from 1 to 10.

  8. Alkylation - Wikipedia

    en.wikipedia.org/wiki/Alkylation

    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.

  9. Category:Alkyl groups - Wikipedia

    en.wikipedia.org/wiki/Category:Alkyl_groups

    Category. : Alkyl groups. Alkyl groups are saturated hydrocarbons substituents with the general formula C n H 2n+1 . Wikimedia Commons has media related to Alkyl groups.