Related Experiment Video

Updated: Jul 31, 2026

Establishment of a Mouse Severe Acute Pancreatitis Model using Retrograde Injection of Sodium Taurocholate into the Biliopancreatic Duct
07:10

Establishment of a Mouse Severe Acute Pancreatitis Model using Retrograde Injection of Sodium Taurocholate into the Biliopancreatic Duct

Published on: April 1, 2022

[Ethanol-oxidizing enzymes of the adrenal glands in acute alcoholic intoxication]

V K Mamedov, Iu E Morozov, E Iu Pigolkina

    Sudebno-Meditsinskaia Ekspertiza
    |September 3, 2004
    PubMed

    More Related Videos

    Chronic Intermittent Ethanol Vapor Exposure Paired with Two-Bottle Choice to Model Alcohol Use Disorder05:12

    Chronic Intermittent Ethanol Vapor Exposure Paired with Two-Bottle Choice to Model Alcohol Use Disorder

    Published on: June 23, 2023

    Assessment of Glutamine as a Fuel Source for Alveolar Macrophages Exposed to Chronic Ethanol Using an Extracellular Flux Bioanalyzer08:37

    Assessment of Glutamine as a Fuel Source for Alveolar Macrophages Exposed to Chronic Ethanol Using an Extracellular Flux Bioanalyzer

    Published on: November 15, 2024

    Related Concept Videos

    Acid-Catalyzed Dehydration of Alcohols to Alkenes02:35

    Acid-Catalyzed Dehydration of Alcohols to Alkenes

    In a dehydration reaction, a hydroxyl group in an alcohol is eliminated along with the hydrogen from an adjacent carbon. Here, the products are an alkene and a molecule of water. Dehydration of alcohols is generally achieved by heating in the presence of an acid catalyst. While the dehydration of primary alcohols requires high temperatures and acid concentrations, secondary and tertiary alcohols can lose a water molecule under relatively mild conditions.
    Oxidation of Alcohols02:37

    Oxidation of Alcohols

    In this lesson, the oxidation of alcohols is discussed in depth. The various reagents used for oxidation of primary and secondary alcohols are detailed, and their mechanism of action is provided.
    The process of oxidation in a chemical reaction is observed in any of the three forms:
    Preparation of Aldehydes and Ketones from Alcohols, Alkenes, and Alkynes01:33

    Preparation of Aldehydes and Ketones from Alcohols, Alkenes, and Alkynes

    Aldehydes and ketones are prepared from alcohols, alkenes, and alkynes via different reaction pathways. Alcohols are the most commonly used substrates for synthesizing aldehydes and ketones. The conversion of alcohol to aldehyde, which involves the oxidation process, depends on the class of the alcohol used and the strength of the oxidizing agent. For instance, primary alcohol will form an aldehyde when treated with a weak oxidizing agent; however, it gets over-oxidized to a carboxylic acid in...
    Aldehydes and Ketones with Alcohols: Hemiacetal Formation01:19

    Aldehydes and Ketones with Alcohols: Hemiacetal Formation

    Similar to water, alcohols can add to the carbonyl carbon of the aldehydes and ketones. The addition of one molecule of alcohol to the carbonyl compound forms the hemiacetal or half acetal. As depicted below, in a hemiacetal, the carbon is directly linked to an OH and OR group.
    Dehydration of Aldols to Enals: Base-Catalyzed Aldol Condensation01:14

    Dehydration of Aldols to Enals: Base-Catalyzed Aldol Condensation

    This lesson delves into the aldol condensation catalyzed by bases, where aldols undergo dehydration to enals. As shown in Figure 1, the β-hydroxy aldehyde formed in a base-catalyzed aldol addition reaction dehydrates on heating to yield an unsaturated carbonyl product, which is commonly referred to as an enal.
    Dehydration of Aldols to Enones: Acid-Catalyzed Aldol Condensation00:43

    Dehydration of Aldols to Enones: Acid-Catalyzed Aldol Condensation

    As shown in Figure 1, under acidic conditions, the β-hydroxy ketone undergoes dehydration via an E1 elimination reaction to form an enone.