Watts Dictionary of Chemistry volume 1
Watts Dictionary of Chemistry volume 1
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From very dilute aqueous amido- benzene m-sulphonic acid and bromine-water (Langfurth, A. 191, 176). 5. From (1, 3, 4, 6)-di- bromo-w-amido-benzene sulphonic acid, fuming HC1, and red P at 150 (Limpricht, B. 10, 1542). 6. By heating the same acid with water at 250 (L. ).
Properties. Anhydrous needles (from cone, aqueous solution) or four- and six-sided columns containing aq (from dilute solution). SI. Sol. Alcohol. Keduced by HI and P, or by water at 120, to amido-benzene m-sulphonic acid.
S al... t s. KA'l aq (La. ). KA' aq (Spiegelberg, A. 197, 257). BaA' 2 aq. BaA' 2 3aq. S. (ofBaA' 2 ) 6-22 at 17. PbA' 2 . CaA' 2 2aq. AgA' laq.
(1, 4, 3)-Bromo-amido-benzene sulphonic acid C u H, Br(NH 2 )S0 3 H [1:4:3]. S. -47 at 15.
Formation. I. By heating ^-bromo-aniline ethyl-sulphate (Nolting, B. 8, 1095). 2. By adding bromine to a cold aqueous solution of barium aniline o-sulphonate (Limpricht, A. 181, 196). 3. By nitration and reduction of bromo- benzene m-sulphonic acid (Thomas, A. 186, 126).
What to read after Watts Dictionary of Chemistry volume 1?
You can find similar books in the "Read Also" column, or choose other free books by Henry Watts to read onlineMoreLess
To quickly assess the difficulty of the text, read a short excerpt:
From very dilute aqueous amido- benzene m-sulphonic acid and bromine-water (Langfurth, A. 191, 176). 5. From (1, 3, 4, 6)-di- bromo-w-amido-benzene sulphonic acid, fuming HC1, and red P at 150 (Limpricht, B. 10, 1542). 6. By heating the same acid with water at 250 (L. ).
Properties. Anhydrous needles (from cone, aqueous solution) or four- and six-sided columns containing aq (from dilute solution). SI. Sol. Alcohol. Keduced by HI and P, or by water at 120, to amido-benzene m-sulphonic acid.
S al... t s. KA'l aq (La. ). KA' aq (Spiegelberg, A. 197, 257). BaA' 2 aq. BaA' 2 3aq. S. (ofBaA' 2 ) 6-22 at 17. PbA' 2 . CaA' 2 2aq. AgA' laq.
(1, 4, 3)-Bromo-amido-benzene sulphonic acid C u H, Br(NH 2 )S0 3 H [1:4:3]. S. -47 at 15.
Formation. I. By heating ^-bromo-aniline ethyl-sulphate (Nolting, B. 8, 1095). 2. By adding bromine to a cold aqueous solution of barium aniline o-sulphonate (Limpricht, A. 181, 196). 3. By nitration and reduction of bromo- benzene m-sulphonic acid (Thomas, A. 186, 126).
What to read after Watts Dictionary of Chemistry volume 1?
You can find similar books in the "Read Also" column, or choose other free books by Henry Watts to read onlineMoreLess
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