Related Experiment Video

Updated: Aug 5, 2026

Method of Direct Segmental Intra-hepatic Delivery Using a Rat Liver Hilar Clamp Model
09:22

Method of Direct Segmental Intra-hepatic Delivery Using a Rat Liver Hilar Clamp Model

Published on: April 2, 2017

Separation and partial characterization of multiple forms of rat liver alcohol dehydrogenase

E Mezey, J J Potter

    Archives of Biochemistry and Biophysics
    |September 1, 1983
    PubMed

    More Related Videos

    Preparation of SNS Cobalt(II) Pincer Model Complexes of Liver Alcohol Dehydrogenase06:31

    Preparation of SNS Cobalt(II) Pincer Model Complexes of Liver Alcohol Dehydrogenase

    Published on: March 19, 2020

    Isolation of Primary Rat Hepatocytes with Multiparameter Perfusion Control07:35

    Isolation of Primary Rat Hepatocytes with Multiparameter Perfusion Control

    Published on: April 5, 2021

    Related Concept Videos

    Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

    Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

    Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
    The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
    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.
    Alcohols from Carbonyl Compounds: Reduction02:23

    Alcohols from Carbonyl Compounds: Reduction

    Reduction is a simple strategy to convert a carbonyl group to a hydroxyl group. The three major pathways to reduce carbonyls to alcohols are catalytic hydrogenation, hydride reduction, and borane reduction.
    Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
    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.