Related Experiment Video

Updated: Jun 5, 2026

Continuous Flow Chemistry: Reaction of Diphenyldiazomethane with p-Nitrobenzoic Acid
07:06

Continuous Flow Chemistry: Reaction of Diphenyldiazomethane with p-Nitrobenzoic Acid

Published on: November 15, 2017

3,4-Dihydr-oxy-N'-(2-hydroxy-benzyl-idene)benzohydrazide-methanol-water (2/1/3)

Hong-Bo Ma, Shan-Shan Huang, Yun-Peng Diao

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

    More Related Videos

    Electroactive Polymer Nanoparticles Exhibiting Photothermal Properties10:16

    Electroactive Polymer Nanoparticles Exhibiting Photothermal Properties

    Published on: January 8, 2016

    Protocol for the Synthesis of Ortho-trifluoromethoxylated Aniline Derivatives08:43

    Protocol for the Synthesis of Ortho-trifluoromethoxylated Aniline Derivatives

    Published on: January 19, 2016

    Related Concept Videos

    Formation of Halohydrin from Alkenes02:41

    Formation of Halohydrin from Alkenes

    An alkene, such as propene, reacts with bromine in the presence of water to yield a halohydrin. Halohydrins contain a halogen and a hydroxyl group attached to adjacent carbons. When the halogen is bromine, it is called a bromohydrin, while a chlorohydrin has chlorine as the halogen.
    Preparation of Alcohols via Addition Reactions02:15

    Preparation of Alcohols via Addition Reactions

    Overview
    The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
    Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration02:34

    Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration

    The rate of acid-catalyzed hydration of alkenes depends on the alkene's structure, as the presence of alkyl substituents at the double bond can significantly influence the rate.
    Hydroboration-Oxidation of Alkenes03:08

    Hydroboration-Oxidation of Alkenes

    In addition to the oxymercuration–demercuration method, which converts the alkenes to alcohols with Markovnikov orientation, a complementary hydroboration-oxidation method yields the anti-Markovnikov product. The hydroboration reaction, discovered in 1959 by H.C. Brown, involves the addition of a B–H bond of borane to an alkene giving an organoborane intermediate. The oxidation of this intermediate with basic hydrogen peroxide forms an alcohol.
    Hydrolysis of Chlorobenzene to Phenol: Dow Process01:10

    Hydrolysis of Chlorobenzene to Phenol: Dow Process

    Simple aryl halides do not react with nucleophiles under normal conditions. However, the reaction can proceed under drastic conditions involving high temperatures and high pressure to give the substituted products. For example, chlorobenzene is converted to phenol using aqueous sodium hydroxide at 350 °C under high pressure by the Dow process. The reaction follows an elimination-addition mechanism involving a benzyne intermediate. Here, the chloride ion is eliminated to generate the benzyne...
    Oxymercuration-Reduction of Alkenes02:36

    Oxymercuration-Reduction of Alkenes

    Oxymercuration–reduction of alkenes is one of the major reactions converting alkenes to alcohols. It involves the hydration of alkenes with mercuric acetate in a mixture of tetrahydrofuran and water, forming an organomercury adduct. This is followed by a demercuration step in which the adduct is reduced to an alcohol using sodium borohydride.