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  2. Azine - Wikipedia

    en.wikipedia.org/wiki/Azine

    Ketazines are also important intermediates in the industrial production of hydrazine hydrate by the peroxide process. [3] In the presence of an oxidant, ammonia and ketones react to give hydrazine via ketazine: 2 Me(Et)C=O + 2 NH 3 + H 2 O 2 → Me(Et)C=NN=C(Et)Me + 2 H 2 O. The ketazine can be hydrolyzed to the hydrazine and regenerate the ketone:

  3. Hydrazone - Wikipedia

    en.wikipedia.org/wiki/Hydrazone

    Hydrazine, organohydrazines, and 1,1-diorganohydrazines react with aldehydes and ketones to give hydrazones. Phenylhydrazine reacts with reducing sugars to form hydrazones known as osazones , which was developed by German chemist Emil Fischer as a test to differentiate monosaccharides .

  4. Acetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde

    Acetaldehyde is an important precursor to pyridine derivatives, pentaerythritol, and crotonaldehyde. Urea and acetaldehyde combine to give a useful resin. Acetic anhydride reacts with acetaldehyde to give ethylidene diacetate, a precursor to vinyl acetate, which is used to produce polyvinyl acetate. [24] The global market for acetaldehyde is ...

  5. Wolff–Kishner reduction - Wikipedia

    en.wikipedia.org/wiki/Wolff–Kishner_reduction

    The Wolff–Kishner reduction is a reaction used in organic chemistry to convert carbonyl functionalities into methylene groups. [1] [2] In the context of complex molecule synthesis, it is most frequently employed to remove a carbonyl group after it has served its synthetic purpose of activating an intermediate in a preceding step.

  6. Enders SAMP/RAMP hydrazone-alkylation reaction - Wikipedia

    en.wikipedia.org/wiki/Enders_SAMP/RAMP_hydrazone...

    The Enders SAMP/RAMP hydrazone alkylation begins with the synthesis of the hydrazone from a N,N-dialkylhydrazine and a ketone or aldehyde [14]. The hydrazone is then deprotonated on the α-carbon position by a strong base, such as lithium diisopropylamide (LDA), leading to the formation of a resonance stabilized anion - an azaenolate.

  7. Reductive amination - Wikipedia

    en.wikipedia.org/wiki/Reductive_amination

    First, the nickel metal dehydrogenates the alcohol to form a ketone and Ni-H complex. Then, the ketone reacts with ammonia to form an imine. Finally, the imine reacts with Ni-H to regenerate catalyst and form primary amine. An example of a homogeneous catalytic system is the reductive amination of ketones done with an iridium catalyst. [20]

  8. AOL Mail - AOL Help

    help.aol.com/products/aol-webmail

    Get answers to your AOL Mail, login, Desktop Gold, AOL app, password and subscription questions. Find the support options to contact customer care by email, chat, or phone number.

  9. Hydrazine - Wikipedia

    en.wikipedia.org/wiki/Hydrazine

    Hydrazine is an inorganic compound with the chemical formula N 2 H 4.It is a simple pnictogen hydride, and is a colourless flammable liquid with an ammonia-like odour.Hydrazine is highly hazardous unless handled in solution as, for example, hydrazine hydrate (N 2 H 4 ·xH 2 O).