関連する実験動画

Updated: Aug 10, 2026

Measuring Rates of Herbicide Metabolism in Dicot Weeds with an Excised Leaf Assay
10:49

Measuring Rates of Herbicide Metabolism in Dicot Weeds with an Excised Leaf Assay

Published on: September 7, 2015

リンダン:ペンタクロロサイクロヘキセネクセンの新しい同位体への代謝

W T Reed, A J Forgash

    Science (New York, N.Y.)
    |June 14, 1968
    PubMed
    まとめ

    研究者らは,室内ハエのリンダンの代謝から2つのペンタクロロサイクロヘクセン同位体を見出した. 1つの同位体は既知の代謝産物であり, 2番目の同位体は,殺虫剤代謝研究における新しい発見を表しています.

    さらに関連する動画

    Analysis of Organochlorine Pesticides in a Soil Sample by a Modified QuEChERS Approach Using Ammonium Formate04:17

    Analysis of Organochlorine Pesticides in a Soil Sample by a Modified QuEChERS Approach Using Ammonium Formate

    Published on: January 20, 2023

    Elucidating the Metabolism of 2,4-Dibromophenol in Plants06:54

    Elucidating the Metabolism of 2,4-Dibromophenol in Plants

    Published on: February 10, 2023

    関連する概念動画

    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.
    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,...
    Halogenation of Alkenes02:46

    Halogenation of Alkenes

    Halogenation is the addition of chlorine or bromine across the double bond in an alkene to yield a vicinal dihalide. The reaction occurs in the presence of inert and non-nucleophilic solvents, such as methylene chloride, chloroform, or carbon tetrachloride.
    Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
    [3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement01:21

    [3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement

    The Cope rearrangement is classified as a [3,3] sigmatropic shift in 1,5-dienes, leading to a more stable, isomeric 1,5-diene. The reaction involves a concerted movement of six electrons, four from two π bonds and two from a σ bond, via an energetically favorable chair-like transition state.
    Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism01:18

    Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism

    Birch reduction uses solvated electrons as reducing agents. The reaction converts benzene to 1,4-cyclohexadiene. The reaction proceeds by the transfer of a single electron to the ring to form a benzene radical anion. This anion is highly basic—it abstracts a proton from the alcohol to form a cyclohexadienyl radical. Another single electron transfer gives the cyclohexadienyl anion. A proton transfer from the alcohol forms 1,4-cyclohexadiene. Since this reduction occurs via radical anion...
    Microbial Bioremediation of Pesticides01:28

    Microbial Bioremediation of Pesticides

    Pesticides often feature structurally complex chemical architectures, incorporating halogen groups and multiple aromatic rings. These characteristics confer high chemical stability, rendering many pesticides resistant to natural degradation processes. This resistance poses significant environmental concerns, as persistent pesticide residues can accumulate in ecosystems and affect non-target organisms.Despite the inherent stability of many pesticides, certain microorganisms possess the metabolic...