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  2. Bromomethane - Wikipedia

    en.wikipedia.org/wiki/Bromomethane

    Infobox references. Bromomethane, commonly known as methyl bromide, is an organobromine compound with formula C H 3 Br. This colorless, odorless, nonflammable gas is produced both industrially and biologically. It is a recognized ozone-depleting chemical.

  3. Angelita C. et al. v. California Department of Pesticide ...

    en.wikipedia.org/wiki/Angelita_C._et_al._v...

    Methyl bromide is a neurotoxin. Accidental poisonings with methyl bromide have been recorded, but few cases documented the concentrations or duration of exposure. It is practically odorless, even at lethal doses, and can cause headaches, mental disturbances, nausea, vomiting and lung edema.

  4. Steric effects - Wikipedia

    en.wikipedia.org/wiki/Steric_effects

    Steric effects arise from the spatial arrangement of atoms. When atoms come close together there is generally a rise in the energy of the molecule. Steric effects are nonbonding interactions that influence the shape (conformation) and reactivity of ions and molecules. Steric effects complement electronic effects, which dictate the shape and ...

  5. File:Effect of methyl bromide additions on the flame speed of ...

    en.wikipedia.org/wiki/File:Effect_of_methyl...

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  6. Haloalkane - Wikipedia

    en.wikipedia.org/wiki/Haloalkane

    For example, the chlorofluorocarbons have been shown to lead to ozone depletion. Methyl bromide is a controversial fumigant. Only haloalkanes that contain chlorine, bromine, and iodine are a threat to the ozone layer , but fluorinated volatile haloalkanes in theory may have activity as greenhouse gases .

  7. Chemical cartridge - Wikipedia

    en.wikipedia.org/wiki/Chemical_cartridge

    Chemical cartridge. A respirator cartridge or gas mask canister is a type of filter that removes gases, volatile organic compounds (VOCs), and other vapors from air through adsorption, absorption, or chemisorption. It is one of two basic types of filters used by air-purifying respirators.

  8. Hunsdiecker reaction - Wikipedia

    en.wikipedia.org/wiki/Hunsdiecker_reaction

    RXNO:0000106. The Hunsdiecker reaction (also called the Borodin reaction or the Hunsdiecker–Borodin reaction) is a name reaction in organic chemistry whereby silver salts of carboxylic acids react with a halogen to produce an organic halide. [1] It is an example of both a decarboxylation and a halogenation reaction as the product has one ...

  9. Free-radical halogenation - Wikipedia

    en.wikipedia.org/wiki/Free-radical_halogenation

    Free-radical halogenation. In organic chemistry, free-radical halogenation is a type of halogenation. This chemical reaction is typical of alkanes and alkyl -substituted aromatics under application of UV light. The reaction is used for the industrial synthesis of chloroform (CHCl 3), dichloromethane (CH 2 Cl 2), and hexachlorobutadiene.