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  2. Acetamide - Wikipedia

    en.wikipedia.org/wiki/Acetamide

    Acetamide (systematic name: ethanamide) is an organic compound with the formula CH 3 CONH 2. It is an amide derived from ammonia and acetic acid. It finds some use as a plasticizer and as an industrial solvent. [5] The related compound N,N-dimethylacetamide (DMA) is more widely used, but it is not

  3. Acetamidine hydrochloride - Wikipedia

    en.wikipedia.org/wiki/Acetamidine_hydrochloride

    Acetamidine hydrochloride is a hygroscopic solid which forms colourless monoclinic crystals. [1] It is soluble in water and alcohol. It releases ammonium chloride upon heating. Dry acetamidine hydrochloride releases acetonitrile, while in aqueous solution, it instead undergoes hydrolysis to acetic acid and ammonia. [3] CH 3 C(NH)NH 2 ·HCl → ...

  4. Bis(trimethylsilyl)acetamide - Wikipedia

    en.wikipedia.org/wiki/Bis(trimethylsilyl)acetamide

    It is a colorless liquid that is soluble in diverse organic solvents, but reacts rapidly with moisture and solvents containing OH and NH groups. It is used in analytical chemistry to increase the volatility of analytes, e.g., for gas chromatography. [1] It is also used to introduce the trimethylsilyl protecting group in organic synthesis. [2]

  5. Metal bis(trimethylsilyl)amides - Wikipedia

    en.wikipedia.org/wiki/Metal_bis(trimethylsilyl...

    For this reason, they are soluble in a range of nonpolar organic solvents, in contrast to simple metal halides, which only dissolve in reactive solvents. These steric bulky complexes are molecular, consisting of mono-, di-, and tetramers. Having a built-in base, these compounds conveniently react with even weakly protic reagents. [1]

  6. Dimethylacetamide - Wikipedia

    en.wikipedia.org/wiki/Dimethylacetamide

    The chemical reactions of dimethylacetamide are typical of N,N-disubstituted amides. Hydrolysis of the acyl-N bond occurs in the presence of acids: CH 3 CON(CH 3) 2 + H 2 O + HCl → CH 3 COOH + (CH 3) 2 NH 2 + Cl −. However, it is resistant to bases. For this reason DMA is a useful solvent for reactions involving strong bases such as sodium ...

  7. Hildebrand solubility parameter - Wikipedia

    en.wikipedia.org/wiki/Hildebrand_solubility...

    (However, PE only dissolves at temperatures well above 100 °C.) Poly(styrene) has a solubility parameter of 9.1 cal 1/2 cm −3/2, and thus ethyl acetate is likely to be a good solvent. Nylon 6,6 has a solubility parameter of 13.7 cal 1/2 cm −3/2, and ethanol is likely to be the best solvent of those tabulated. However, the latter is polar ...

  8. Acyl group - Wikipedia

    en.wikipedia.org/wiki/Acyl_group

    (R 1, R 2 and R 3 stands for organyl substituent or hydrogen in the case of R 1) In chemistry, an acyl group is a moiety derived by the removal of one or more hydroxyl groups from an oxoacid, [1] including inorganic acids. It contains a double-bonded oxygen atom and an organyl group (R−C=O) or hydrogen in the case of formyl group (H−C=O).

  9. Williamson ether synthesis - Wikipedia

    en.wikipedia.org/wiki/Williamson_ether_synthesis

    The Williamson ether reaction follows an S N 2 (bimolecular nucleophilic substitution) mechanism. In an S N 2 reaction mechanism there is a backside attack of an electrophile by a nucleophile and it occurs in a concerted mechanism (happens all at once). In order for the S N 2 reaction to take place there must be a good leaving group which is ...