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  2. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    The term alkyl is intentionally unspecific to include many possible substitutions. An acyclic alkyl has the general formula of −C n H 2n+1. 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.

  3. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    An alkyl group is an alkane-based molecular fragment that bears one open valence for bonding. They are generally abbreviated with the symbol for any organyl group, R, although Alk is sometimes used to specifically symbolize an alkyl group (as opposed to an alkenyl group or aryl group).

  4. Carbonate ester - Wikipedia

    en.wikipedia.org/wiki/Carbonate_ester

    Carbonate esters can be divided into three structural classes: acyclic, cyclic, and polymeric. The first and general case is the acyclic carbonate group. Organic substituents can be identical or not. Both aliphatic or aromatic substituents are known, they are called dialkyl or diaryl carbonates, respectively.

  5. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Acyclic aliphatic/non-aromatic compound Cyclic aliphatic/non-aromatic compound (cyclobutane)In organic chemistry, hydrocarbons (compounds composed solely of carbon and hydrogen) are divided into two classes: aromatic compounds and aliphatic compounds (/ ˌ æ l ɪ ˈ f æ t ɪ k /; G. aleiphar, fat, oil).

  6. Neighbouring group participation - Wikipedia

    en.wikipedia.org/wiki/Neighbouring_group...

    In this type of substitution reaction, one group of the substrate participates initially in the reaction and thereby affects the reaction. A classic example of NGP is the reaction of a sulfur or nitrogen mustard with a nucleophile, the rate of reaction is much higher for the sulfur mustard and a nucleophile than it would be for a primary or secondary alkyl chloride without a heteroatom.

  7. Cyclic alkyl amino carbenes - Wikipedia

    en.wikipedia.org/wiki/Cyclic_alkyl_amino_carbenes

    Bicyclic(alkyl)(amino) carbenes (BICAACs) are CAACs containing a bicyclic backbone. The bicyclic system forces the substituents on the carbon to adopt a "fan-like" geometry closer to that of a diamino NHC. [15] As a result, BICAACs show stronger σ-donating and π-accepting properties compared to monocyclic CAACs. [15]

  8. Ketimine Mannich reaction - Wikipedia

    en.wikipedia.org/wiki/Ketimine_Mannich_reaction

    Acyclic ketimines with electron-withdrawing groups and/or alkynes. Esters, perfluorinated alkyl, or alkyne groups are good electrophiles, that can be used to form ...

  9. Woodward's rules - Wikipedia

    en.wikipedia.org/wiki/Woodward's_rules

    In the compound on the left, the base value is 214 nm (a heteroannular diene). This diene group has 4 alkyl substituents (labeled 1,2,3,4) and the double bond in one ring is exocyclic to the other (adding 5 nm for an exocyclic double bond). In the compound on the right, the diene is homoannular with 4 alkyl substituents.