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  2. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    In organic chemistry, a methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms, having chemical formula CH 3 (whereas normal methane has the formula CH 4). In formulas, the group is often abbreviated as Me. This hydrocarbon group occurs in many organic compounds. It is a very stable group in ...

  3. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    IUPAC name: Common name: Structural formula octanoic acid: caprylic acid: CH 3 (CH 2) 6 COOH benzene-1,2-dicarboxylic acid: phthalic acid: C 6 H 4 (COOH) 2: benzene-1,3-dicarboxylic acid: isophthalic acid: C 6 H 4 (COOH) 2: benzene-1,4-dicarboxylic acid: terephthalic acid: C 6 H 4 (COOH) 2: 2-methylheptanoic acid C 5 H 11 CH(CH 3)COOH 3 ...

  4. Methyl radical - Wikipedia

    en.wikipedia.org/wiki/Methyl_radical

    It can also be produced by the reaction of methane with the hydroxyl radical: OH • + CH 4 → CH • 3 + H 2 O. This process begins the major removal mechanism of methane from the atmosphere. The reaction occurs in the troposphere or stratosphere. In addition to being the largest known sink for atmospheric methane, this reaction is one of the ...

  5. Methenium - Wikipedia

    en.wikipedia.org/wiki/Methenium

    In organic chemistry, methenium (also called methylium, carbenium, [2] methyl cation, or protonated methylene) is a cation with the formula CH + 3. It can be viewed as a methylene radical (: CH 2) with an added proton (H +), or as a methyl radical (• CH 3) with one electron removed.

  6. Methyl acetate - Wikipedia

    en.wikipedia.org/wiki/Methyl_acetate

    The conversion of methyl acetate back into its components, by an acid, is a first-order reaction with respect to the ester. 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.

  7. Crotonaldehyde - Wikipedia

    en.wikipedia.org/wiki/Crotonaldehyde

    Crotonaldehyde is a chemical compound with the formula CH 3 CH=CHCHO. The compound is usually sold as a mixture of the E- and Z-isomers, which differ with respect to the relative position of the methyl and formyl groups. The E-isomer is more common (data given in Table is for the E-isomer).

  8. IUPAC nomenclature of organic chemistry - Wikipedia

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

    The alkyl (R') group is named first. The R−C(=O)O part is then named as a separate word based on the carboxylic acid name, with the ending changed from "-oic acid" to "-oate" or "-carboxylate" For example, CH 3 CH 2 CH 2 CH 2 COOCH 3 is methyl pentanoate, and (CH 3) 2 CHCH 2 CH 2 COOCH 2 CH 3 is ethyl 4-methylpentanoate.

  9. Trimethylborane - Wikipedia

    en.wikipedia.org/wiki/Trimethylborane

    Trimethylborane is a strong Lewis acid. B(CH 3) 3 can form an adduct with ammonia: (NH 3):B(CH 3) 3. [13] as well as other Lewis bases. The Lewis acid properties of B(CH 3) 3 have been analyzed by the ECW model yielding E A = 2.90 and C A = 3.60.