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  2. List of esters - Wikipedia

    en.wikipedia.org/wiki/List_of_esters

    Esters of carboxylic acids with low molecular weight are commonly used as fragrances and found in essential oils and pheromones. Phosphoesters form the backbone of DNA molecules. Nitrate esters, such as nitroglycerin, are known for their explosive properties, while polyesters are important plastics, with monomers linked by ester moieties.

  3. Category:Chromates - Wikipedia

    en.wikipedia.org/wiki/Category:Chromates

    Cadmium chromate; Caesium chromate; Calcium chromate; Chromate ester; Chromated copper arsenate; Template:Chromates and dichromates; Chrome orange; Chrome yellow; Chromic acid; Chromium(VI) oxide peroxide

  4. Chromate ester - Wikipedia

    en.wikipedia.org/wiki/Chromate_ester

    A chromate ester is a chemical structure that contains a chromium atom (symbol Cr) in a +6 oxidation state that is connected via an oxygen (O) linkage to a carbon (C) atom. The Cr itself is in its chromate form, with several oxygens attached, and the Cr–O–C attachment makes this chemical group structurally similar to other ester functional groups.

  5. List of food additives - Wikipedia

    en.wikipedia.org/wiki/List_of_food_additives

    Tartaric acid esters of mono- and diglycerides of fatty acids – emulsifier Tartrazine – color (yellow and orange) ( FDA : FD&C Yellow #5) Tea oil /Camellia oil – widely used in southern China as a cooking oil.

  6. Category:Esters - Wikipedia

    en.wikipedia.org/wiki/Category:Esters

    In organic chemistry and biochemistry esters are the functional group (R'-COOR") consisting of an organic radical united with the residue of any oxygen acid, either organic or inorganic. An ester is a product of the reaction of an acid (usually organic) and an alcohol (the hydrogen of the acid R-COOH is replaced by an alkyl group R").

  7. Template:Chromates and dichromates - Wikipedia

    en.wikipedia.org/wiki/Template:Chromates_and_di...

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  8. Jones oxidation - Wikipedia

    en.wikipedia.org/wiki/Jones_oxidation

    Like conventional esters, the formation of this chromate ester is accelerated by the acid. These esters can be isolated when the alcohol is tertiary because these lack the α hydrogen that would be lost to form the carbonyl. For example, using tert-butyl alcohol, one can isolate tert-butyl chromate ((CH 3) 3 CO) 2 CrO 2), which is itself a good ...

  9. Chromic acid - Wikipedia

    en.wikipedia.org/wiki/Chromic_acid

    Partial predominance diagram for chromate. Molecular chromic acid, H 2 CrO 4, in principle, resembles sulfuric acid, H 2 SO 4. It would ionize accordingly: H 2 CrO 4 ⇌ [HCrO 4] − + H + The pK a for the equilibrium is not well characterized. Reported values vary between about −0.8 to 1.6. [4]