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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. 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.

  4. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    is an alkaline solution of potassium permanganate; used in organic chemistry as a qualitative test for the presence of unsaturation, such as double bonds; N-Bromosuccinimide: used in radical substitution and electrophilic addition reactions in organic chemistry. Also acts as a mild oxidizer to oxidize benzylic or allylic alcohols.

  5. Conjugate (acid-base theory) - Wikipedia

    en.wikipedia.org/wiki/Conjugate_(acid-base_theory)

    An example of this case would be the splitting of hydrochloric acid HCl in water. Since HCl is a strong acid (it splits up to a large extent), its conjugate base (Cl −) will be weak. Therefore, in this system, most H + will be hydronium ions H 3 O + instead of attached to Cl − anions and the conjugate bases will be weaker than water molecules.

  6. Methyl tert-butyl ether - Wikipedia

    en.wikipedia.org/wiki/Methyl_tert-butyl_ether

    Methyl tert-butyl ether (MTBE), also known as tert-butyl methyl ether, is an organic compound with a structural formula (CH 3) 3 COCH 3.MTBE is a volatile, flammable, and colorless liquid that is sparingly soluble in water. [1]

  7. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    For example, (CH 3) 2 CHCH 2 CH 3 (isopentane) is named 2-methylbutane, not 3-methylbutane. If there are multiple side-branches of the same size alkyl group, their positions are separated by commas and the group prefixed with multiplier prefixes depending on the number of branches. For example, C(CH 3) 4 (neopentane) is named 2,2 ...

  8. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    1.174 546 744 990 17 × 10 19: C 46 H 94: n-hexatetracontane: 47 58 481 806 621 987 010: 3.659 736 342 498 25 × 10 19: C 47 H 96: n-heptatetracontane: 48 156 192 366 474 590 639: 1.141 606 809 779 03 × 10 20: C 48 H 98: n-octatetracontane: 49 417 612 400 765 382 272: 3.564 926 050 353 17 × 10 20: C 49 H 100: n-nonatetracontane: 50 1 117 743 ...

  9. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    For example, the main constituent of white vinegar is CH 3 COOH , which is commonly called acetic acid and is also its recommended IUPAC name, but its formal, systematic IUPAC name is ethanoic acid. The IUPAC's rules for naming organic and inorganic compounds are contained in two publications, known as the Blue Book [ 1 ] [ 2 ] and the Red Book ...

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