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  2. Salt metathesis reaction - Wikipedia

    en.wikipedia.org/wiki/Salt_metathesis_reaction

    A neutralization reaction is a type of double replacement reaction. A neutralization reaction occurs when an acid reacts with an equal amount of a base. This reaction usually produces a salt. One example, hydrochloric acid reacts with disodium iron tetracarbonyl to produce the iron dihydride: 2 HCl + Na 2 Fe(CO) 4 → 2 NaCl + H 2 Fe(CO) 4

  3. 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 ...

  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. 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.

  6. Mesylate - Wikipedia

    en.wikipedia.org/wiki/Mesylate

    In organosulfur chemistry, a mesylate is any salt or ester of methanesulfonic acid (CH 3 SO 3 H). In salts, the mesylate is present as the CH 3 SO − 3 anion . When modifying the international nonproprietary name of a pharmaceutical substance containing the group or anion, the spelling used is sometimes mesilate (as in imatinib mesilate , the ...

  7. Methanethiol - Wikipedia

    en.wikipedia.org/wiki/Methanethiol

    It is a weak acid, with a pK a of ~10.4, but is about a hundred thousand times more acidic than methanol. The colorless salt can be obtained in this way: CH 3 SH + CH 3 ONa → CH 3 SNa + CH 3 OH. The resulting thiolate anion is a strong nucleophile. It can be oxidized to dimethyl disulfide: 2CH 3 SH + [O] → CH 3 SSCH 3 + H 2 O

  8. Acid salt - Wikipedia

    en.wikipedia.org/wiki/Acid_salt

    An acid salt can be mixed with certain base salt (such as sodium bicarbonate or baking soda) to create baking powders which release carbon dioxide. [10] Leavening agents can be slow-acting (e.g. sodium aluminum phosphate) which react when heated, or fast-acting (e.g., cream of tartar) which react immediately at low temperatures. Double-acting ...

  9. 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).