Related Experiment Video

Updated: Jun 5, 2026

Facile Preparation of (2Z,4E)-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate
06:46

Facile Preparation of (2Z,4E)-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate

Published on: June 21, 2017

2,6-Dimethyl-4-m-tolyl-cyclo-hex-3-enecarboxylic acid

Songwen Xie, Holly J Stein, Maren Pink

    Acta Crystallographica. Section E, Structure Reports Online
    |January 5, 2011
    PubMed

    More Related Videos

    Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyl(tropone)iron07:56

    Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyl(tropone)iron

    Published on: August 12, 2019

    Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers08:12

    Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

    Published on: December 16, 2022

    Related Concept Videos

    Disubstituted Cyclohexanes: cis-trans Isomerism02:37

    Disubstituted Cyclohexanes: cis-trans Isomerism

    Depending upon the different spatial orientation of the substituents, the disubstituted cycloalkanes exhibit two types of stereoisomers. The cis isomers have the substituents on the same side of the ring, whereas the trans isomers have the substituents on the opposite sides. These stereoisomers exhibit different physical properties and cannot be interconverted without breaking the carbon-carbon bonds.
    In cyclohexane, the substituents can occupy different positions generating distinct isomers.
    Aromatic Hydrocarbon Cations: Structural Overview01:18

    Aromatic Hydrocarbon Cations: Structural Overview

    Cycloheptatriene is a neutral monocyclic unsaturated hydrocarbon that consists of an odd number of carbon atoms and an intervening sp3 carbon in the ring. The three double bonds in the ring correspond to 6 π electrons, which is a Huckel number, and therefore satisfies the criteria of 4n + 2 π electrons. However, the intervening sp3 carbon disrupts the continuous overlap of p orbitals. As a result, cycloheptatriene is not aromatic.
    Removing one hydrogen from the intervening CH2 group with both...
    IUPAC Nomenclature of Carboxylic Acids01:16

    IUPAC Nomenclature of Carboxylic Acids

    IUPAC names of carboxylic acids are systematically derived following a few rules discussed below.
    For acyclic saturated monocarboxylic acids, the longest hydrocarbon chain containing the –COOH carbon is identified as the parent chain. Then, the last -e of the parent hydrocarbon name is replaced with a suffix -oic acid.
    Loss of Carboxy Group as CO2: Decarboxylation of Malonic Acid Derivatives01:35

    Loss of Carboxy Group as CO2: Decarboxylation of Malonic Acid Derivatives

    Just like β-keto acids—which upon thermal decarboxylation form ketones—β-dicarboxylic acids undergo decarboxylation to generate monocarboxylic acids with the liberation of carbon dioxide.
    Stereoisomerism of Cyclic Compounds02:33

    Stereoisomerism of Cyclic Compounds

    In this lesson, we delve into the role of ring conformation and its stability, which determines the spatial arrangement and, consequently, the molecular symmetry and stereoisomerism of cyclic compounds. 1,2-Dimethylcyclohexane is used as a case study to evaluate the possible number of stereoisomers. Here, given the multiple (n = 2) chiral centers, there are 2n = 4 possible configurations that lack a plane of symmetry, as the ring skeleton exists in a non-planar chair conformation. In addition,...
    Nomenclature of Carboxylic Acid Derivatives: Amides and Nitriles01:11

    Nomenclature of Carboxylic Acid Derivatives: Amides and Nitriles

    Naming Amides
    The IUPAC and common names of amides are derived from the parent carboxylic acid, by replacing the suffix “oic acid” and “ic acid,” respectively, with “amide.” In the following example, the IUPAC name ethanamide is derived from ethanoic acid, and the common name, acetamide, is obtained from acetic acid.