A text-book of inorganic chemistry, by George S Newth

By George S Newth

Initially released in 1894. This quantity from the Cornell college Library's print collections was once scanned on an APT BookScan and switched over to JPG 2000 layout through Kirtas applied sciences. All titles scanned conceal to hide and pages may well contain marks notations and different marginalia found in the unique quantity.

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By George S Newth

Initially released in 1894. This quantity from the Cornell college Library's print collections was once scanned on an APT BookScan and switched over to JPG 2000 layout through Kirtas applied sciences. All titles scanned conceal to hide and pages may well contain marks notations and different marginalia found in the unique quantity.

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5-Methyl-5-hydroxymethyl-l,3,2-dioxathiane 2-oxide (9)reacted similarly, but the corresponding 5, 5-dirnethyl derivative failed to react. According to Brunken and PoppelOC trimethylene m i t e reacts with sulfuric acid to form 3-hydroxypropylsulfuric acid [For references, see pp. 1 649 Chapter 8 H2S04 0 00 ___3 HOCH2CH,CH,OSO,H Cyclic sulfites have been reported to be sufficiently stable to nitric acid to allow nitration of a benzene ring. 47360 lo, The reaction has been used to synthesize chloramphenicol; a variety of amides and mbstituted phenyl compounds were used.

11. 12. 13. Bordwell, F. ,C. M Suter, and A. J. Webber, J. Am. , 67,827 (1945). Bordwell, F. ,and C. , J. A m Chem. ,lO, 2429 (1948). L. Peterson, and C. S. , J. A m Chem. , 76,3945 (1954). , and M. L. Peterson, J. , 76,3952 (1954). Bordwell, F. ,and M. L. Peterson, J. , 18,3957 (1954). Breslow, D. , R R H w g h , and J. T. Fairclough, J. A m Chem. ~,5361 (1954). , and R R Haugh, J. A m Chem. , 79,5000 (1957). , J. Am. Chem. , 67,220 (1945). ,J. Am. ,71, 1769 (1949). ,and k M. S. Patent 2,839,573 (1958); Ger.

2. H2 H2 (15) n2 H2 c-c s--9 c-c 13 I4\ /15 IS\ / I 2\ H2 H2 15 H2 H2 This compound was prepared by both Fredga8 and by Asinger and coworkers. 5-131. 5" and 15 Asinger of 133'. Another instance of the effect of reaction conditions On the products formed in these reactions was indicated by Magnusson,fOa who isolated a 1,2,3,5,6-pentathiepane when the above reaction was carried out at 0-4" in aqueous ethanol. N-C- 16 (RRI 1062) This ring system, which has been reported only in the 1, 5, 6,7tetradehydro form, is indexed in Chemical Abstracts as 2, B-tetrathio1, 3,4-thiadiazole.

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