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  2. Methyl acetate - Wikipedia

    en.wikipedia.org/wiki/Methyl_acetate

    The reaction of methyl acetate and a base, for example sodium hydroxide, is a second-order reaction with respect to both reactants. Methyl acetate is a Lewis base that forms 1:1 adducts with a variety of Lewis acids. It is classified as a hard base and is a base in the ECW model with E B =1.63 and C B = 0.95.

  3. Di-tert-butyl peroxide - Wikipedia

    en.wikipedia.org/wiki/Di-tert-butyl_peroxide

    For this reason di-tert-butyl peroxide is commonly used as a radical initiator in organic synthesis and polymer chemistry. The decomposition reaction proceeds via the generation of methyl radicals. (CH 3) 3 COOC(CH 3) 3 → 2 (CH 3) 3 CO • (CH 3) 3 CO • → (CH 3) 2 CO + CH • 3 2 CH • 3 → C 2 H 6

  4. Acetic anhydride - Wikipedia

    en.wikipedia.org/wiki/Acetic_anhydride

    As indicated by its organic chemistry, acetic anhydride is mainly used for acetylations leading to commercially significant materials. Its largest application is for the conversion of cellulose to cellulose acetate, which is a component of photographic film and other coated materials, and is used in the manufacture of cigarette filters.

  5. Methyl tert-butyl ether - Wikipedia

    en.wikipedia.org/wiki/Methyl_tert-butyl_ether

    MTBE is used in organic chemistry as a relatively inexpensive solvent with properties comparable to diethyl ether, but with a higher boiling point and less solubility in water. As a solvent, MTBE has one distinct advantage over most ethers - it has a much lower tendency to form explosive organic peroxides.

  6. List of compounds with carbon number 3 - Wikipedia

    en.wikipedia.org/wiki/List_of_compounds_with...

    1066-37-1 C 3 H 9 BrPb: trimethyl lead bromide: 6148-48-7 C 3 H 9 BrSi: bromotrimethylsilane: 2857-97-8 C 3 H 9 BrSn: trimethyltin bromide: 1066-44-0 C 3 H 9 Br 2 Sb: trimethylantimony dibromide: 24606-08-4 C 3 H 9 ClFSb: chlorofluorotrimethylantimony: 13077-54-8 C 3 H 9 ClGe: trimethylgermanium chloride: 1529-47-1 C 3 H 9 ClPb: trimethyllead ...

  7. Acetoxy group - Wikipedia

    en.wikipedia.org/wiki/Acetoxy_group

    In organic chemistry, the acetoxy group (abbr. AcO or OAc; IUPAC name: acetyloxy [1]), is a functional group with the formula −OCOCH 3 and the structure −O−C(=O)−CH 3. As the -oxy suffix implies, it differs from the acetyl group (−C(=O)−CH 3) by the presence of an additional oxygen atom. The name acetoxy is the short form of acetyl-oxy.

  8. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    For example, the compound LiBr is made of Li + cations and Br − anions; thus, it is called lithium bromide. The compound BaO, which is composed of Ba 2+ cations and O 2− anions, is referred to as barium oxide. The oxidation state of each element is unambiguous. When these ions combine into a type-I binary compound, their equal-but-opposite ...

  9. Acetyl group - Wikipedia

    en.wikipedia.org/wiki/Acetyl_group

    In organic chemistry, an acetyl group is a functional group denoted by the chemical formula −COCH 3 and the structure −C(=O)−CH 3. It is sometimes represented by the symbol Ac [5] [6] (not to be confused with the element actinium). In IUPAC nomenclature, an acetyl group is called an ethanoyl group.