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  2. Benzamide - Wikipedia

    en.wikipedia.org/wiki/Benzamide

    Benzamide is an organic compound with the chemical formula of C 7 H 7 NO. It is the simplest amide derivative of benzoic acid. In powdered form, it appears as a white solid, while in crystalline form, it appears as colourless crystals. [5] It is slightly soluble in water, [2] and soluble in many organic solvents. [6]

  3. Birch reduction - Wikipedia

    en.wikipedia.org/wiki/Birch_reduction

    The Birch reduction is an organic reaction that is used to convert arenes to 1,4-cyclohexadienes.The reaction is named after the Australian chemist Arthur Birch and involves the organic reduction of aromatic rings in an amine solvent (traditionally liquid ammonia) with an alkali metal (traditionally sodium) and a proton source (traditionally an alcohol).

  4. 3,4,5-Trimethoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/3,4,5-Trimethoxybenzaldehyde

    3,4,5-Trimethoxybenzaldehyde can be used as an intermediate in the synthesis of some pharmaceutical drugs including trimethoprim, [1] [2] cintriamide, roletamide, trimethoquinol (aka tretoquinol), and trimazosin as well as some psychedelic phenethylamines.

  5. Amide - Wikipedia

    en.wikipedia.org/wiki/Amide

    The structure of an amide can be described also as a resonance between two alternative structures: neutral (A) and zwitterionic (B). It is estimated that for acetamide , structure A makes a 62% contribution to the structure, while structure B makes a 28% contribution (these figures do not sum to 100% because there are additional less-important ...

  6. Knorr pyrrole synthesis - Wikipedia

    en.wikipedia.org/wiki/Knorr_pyrrole_synthesis

    The resulting product, diethyl 3,5-dimethylpyrrole-2,4-dicarboxylate, has been called Knorr's Pyrrole ever since. In the Scheme above, R 2 = COOEt, and R 1 = R 3 = Me represent this original reaction. Knorr's pyrrole can be derivatized in a number of useful manners. One equivalent of sodium hydroxide will saponify the 2-ester selectively.

  7. Xylene - Wikipedia

    en.wikipedia.org/wiki/Xylene

    They are derived from the substitution of two hydrogen atoms with methyl groups in a benzene ring; which hydrogens are substituted determines which of three structural isomers results. It is a colorless, flammable, slightly greasy liquid of great industrial value. [3] The mixture is referred to as both xylene and, more precisely, xylenes.

  8. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    The benzyl cation or phenylcarbenium ion is the carbocation with formula C 6 H 5 CH + 2; the benzyl anion or phenylmethanide ion is the carbanion with the formula C 6 H 5 CH − 2. None of these species can be formed in significant amounts in the solution phase under normal conditions, but they are useful referents for discussion of reaction ...

  9. Benzoic acid - Wikipedia

    en.wikipedia.org/wiki/Benzoic_acid

    ɪ k /) is a white (or colorless) solid organic compound with the formula C 6 H 5 COOH, whose structure consists of a benzene ring (C 6 H 6) with a carboxyl (−C(=O)OH) substituent. The benzoyl group is often abbreviated "Bz" (not to be confused with "Bn," which is used for benzyl ), thus benzoic acid is also denoted as BzOH, since the benzoyl ...