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  2. Propanamide - Wikipedia

    en.wikipedia.org/wiki/Propanamide

    This article about an organic compound is a stub. You can help Wikipedia by expanding it.

  3. Syn and anti addition - Wikipedia

    en.wikipedia.org/wiki/Syn_and_anti_addition

    In organic chemistry, syn-and anti-addition are different ways in which substituent molecules can be added to an alkene (R 2 C=CR 2) or alkyne (RC≡CR).The concepts of syn and anti addition are used to characterize the different reactions of organic chemistry by reflecting the stereochemistry of the products in a reaction.

  4. Zaytsev's rule - Wikipedia

    en.wikipedia.org/wiki/Zaytsev's_rule

    For example, when 2-iodobutane is treated with alcoholic potassium hydroxide (KOH), but-2-ene is the major product and but-1-ene is the minor product. [ 1 ] More generally, Zaytsev's rule predicts that in an elimination reaction the most substituted product will be the most stable, and therefore the most favored.

  5. Propionyl chloride - Wikipedia

    en.wikipedia.org/wiki/Propionyl_chloride

    Propionyl chloride (also propanoyl chloride) is the organic compound with the formula CH 3 CH 2 C(O)Cl. It is the acyl chloride derivative of propionic acid.It undergoes the characteristic reactions of acyl chlorides. [1]

  6. Ketone halogenation - Wikipedia

    en.wikipedia.org/wiki/Ketone_halogenation

    Halogenation of α,β-unsaturated ketone [3]. On α,β-Unsaturated ketones or enones, it's possible to halogenate with iodine selectively on the more saturated alpha on the ketone selectively over the unsaturated side.

  7. Hofmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Hofmann_rearrangement

    The Hofmann rearrangement (Hofmann degradation) is the organic reaction of a primary amide to a primary amine with one less carbon atom. [1] [2] [3] The reaction involves oxidation of the nitrogen followed by rearrangement of the carbonyl and nitrogen to give an isocyanate intermediate.

  8. Haloform reaction - Wikipedia

    en.wikipedia.org/wiki/Haloform_reaction

    In chemistry, the haloform reaction (also referred to as the Lieben haloform reaction) is a chemical reaction in which a haloform (CHX 3, where X is a halogen) is produced by the exhaustive halogenation of an acetyl group (R−C(=O)CH 3, where R can be either a hydrogen atom, an alkyl or an aryl group), in the presence of a base.

  9. Cannizzaro reaction - Wikipedia

    en.wikipedia.org/wiki/Cannizzaro_reaction

    2 c 6 h 5 cho + koh → c 6 h 5 ch 2 oh + c 6 h 5 cook The process is a redox reaction involving transfer of a hydride from one substrate molecule to the other: one aldehyde is oxidized to form the acid, the other is reduced to form the alcohol.