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  2. Acetyl chloride - Wikipedia

    en.wikipedia.org/wiki/Acetyl_chloride

    Acetyl chloride was first prepared in 1852 by French chemist Charles Gerhardt by treating potassium acetate with phosphoryl chloride. [4]Acetyl chloride is produced in the laboratory by the reaction of acetic acid with chlorodehydrating agents such as phosphorus trichloride (PCl 3), phosphorus pentachloride (PCl 5), sulfuryl chloride (SO 2 Cl 2), phosgene, or thionyl chloride (SOCl 2).

  3. Chloroacetyl chloride - Wikipedia

    en.wikipedia.org/wiki/Chloroacetyl_chloride

    The major use of chloroacetyl chloride is as an intermediate in the production of herbicides in the chloroacetanilide family including metolachlor, acetochlor, alachlor and butachlor; an estimated 100 million pounds are used annually. Some chloroacetyl chloride is also used to produce phenacyl chloride, another chemical intermediate, also used ...

  4. Flammability diagram - Wikipedia

    en.wikipedia.org/wiki/Flammability_diagram

    Flammability diagrams show the control of flammability in mixtures of fuel, oxygen and an inert gas, typically nitrogen. Mixtures of the three gasses are usually depicted in a triangular diagram, known as a ternary plot. Such diagrams are available in the speciality literature. [ 1][ 2][ 3] The same information can be depicted in a normal ...

  5. Nucleophilic acyl substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_acyl_substitution

    Nucleophilic acyl substitution ( SNAcyl) describes a class of substitution reactions involving nucleophiles and acyl compounds. In this type of reaction, a nucleophile – such as an alcohol, amine, or enolate – displaces the leaving group of an acyl derivative – such as an acid halide, anhydride, or ester. The resulting product is a ...

  6. Peracetic acid - Wikipedia

    en.wikipedia.org/wiki/Peracetic_acid

    Peracetic acid (also known as peroxyacetic acid, or PAA) is an organic compound with the formula CH 3 CO 3 H. This peroxy acid is a colorless liquid with a characteristic acrid odor reminiscent of acetic acid. It can be highly corrosive . Peracetic acid is a weaker acid than the parent acetic acid, with a p Ka of 8.2.

  7. Cellulose acetate - Wikipedia

    en.wikipedia.org/wiki/Cellulose_acetate

    The chemical formula shows a section of cellulose with two acetyl groups per glucose module. In biochemistry, cellulose acetate refers to any acetate ester of cellulose, usually cellulose diacetate. It was first prepared in 1865. [ 1][verification needed] A bioplastic, cellulose acetate is used as a film base in photography, as a component in ...

  8. Acetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde

    Acetaldehyde (IUPAC systematic name ethanal) is an organic chemical compound with the formula CH 3 CHO, sometimes abbreviated as Me CHO. It is a colorless liquid or gas, boiling near room temperature. It is one of the most important aldehydes, occurring widely in nature and being produced on a large scale in industry.

  9. Combustibility and flammability - Wikipedia

    en.wikipedia.org/.../Combustibility_and_flammability

    Combustibility and flammability. A combustible material is a material that can burn (i.e., sustain a flame) in air under certain conditions. A material is flammable if it ignites easily at ambient temperatures. In other words, a combustible material ignites with some effort and a flammable material catches fire immediately on exposure to flame.