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  2. Tollens' reagent - Wikipedia

    en.wikipedia.org/wiki/Tollens'_reagent

    Tollens' reagent (chemical formula ()) is a chemical reagent used to distinguish between aldehydes and ketones along with some alpha-hydroxy ketones which can tautomerize into aldehydes. The reagent consists of a solution of silver nitrate , ammonium hydroxide and some sodium hydroxide (to maintain a basic pH of the reagent solution).

  3. Fehling's solution - Wikipedia

    en.wikipedia.org/wiki/Fehling's_solution

    Monosaccharides. In organic chemistry, Fehling's solution is a chemical reagent used to differentiate between water-soluble carbohydrate and ketone (>C=O) functional groups, and as a test for reducing sugars and non-reducing sugars, supplementary to the Tollens' reagent test. The test was developed by German chemist Hermann von Fehling in 1849.

  4. 2,4-Dinitrophenylhydrazine - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrophenylhydrazine

    2,4-Dinitrophenylhydrazine (2,4-DNPH or DNPH) is the organic compound C 6 H 3 (NO 2) 2 NHNH 2. DNPH is a red to orange solid. It is a substituted hydrazine. The solid is relatively sensitive to shock and friction. For this reason DNPH is usually handled as a wet powder. DNPH is a precursor to the drug Sivifene.

  5. Oxidation state - Wikipedia

    en.wikipedia.org/wiki/Oxidation_state

    Oxidation state. In chemistry, the oxidation state, or oxidation number, is the hypothetical charge of an atom if all of its bonds to other atoms were fully ionic. It describes the degree of oxidation (loss of electrons) of an atom in a chemical compound. Conceptually, the oxidation state may be positive, negative or zero.

  6. Benedict's reagent - Wikipedia

    en.wikipedia.org/wiki/Benedict's_reagent

    Benedict's reagent (often called Benedict's qualitative solution or Benedict's solution) is a chemical reagent and complex mixture of sodium carbonate, sodium citrate, and copper (II) sulfate pentahydrate. [1] It is often used in place of Fehling's solution to detect the presence of reducing sugars and other reducing substances. [2]

  7. Haloform reaction - Wikipedia

    en.wikipedia.org/wiki/Haloform_reaction

    haloform-reaction. RSC ontology ID. RXNO:0000689. In chemistry, the haloform reaction (also referred to as the Lieben haloform reaction) is a chemical reaction in which a haloform (CHX3, where X is a halogen) is produced by the exhaustive halogenation of an acetyl group (R−C (=O)CH3, where R can be either a hydrogen atom, an alkyl or an aryl ...

  8. Silver fulminate - Wikipedia

    en.wikipedia.org/wiki/Silver_fulminate

    Silver fulminate (AgCNO) is the highly explosive silver salt of fulminic acid. Silver fulminate is a primary explosive, but has limited use as such due to its extreme sensitivity to impact, heat, pressure, and electricity. The compound becomes progressively sensitive as it is aggregated, even in small amounts; the touch of a falling feather ...

  9. Ammonia solution - Wikipedia

    en.wikipedia.org/wiki/Ammonia_solution

    Ammonia solution, also known as ammonia water, ammonium hydroxide, ammoniacal liquor, ammonia liquor, aqua ammonia, aqueous ammonia, or (inaccurately) ammonia, is a solution of ammonia in water. It can be denoted by the symbols NH 3 (aq). Although the name ammonium hydroxide suggests a salt with the composition [NH+. 4] [OH−.