{"id":2651,"date":"2007-01-11T00:00:00","date_gmt":"2007-01-10T23:00:00","guid":{"rendered":""},"modified":"-0001-11-30T00:00:00","modified_gmt":"-0001-11-29T22:00:00","slug":"2651","status":"publish","type":"post","link":"https:\/\/www.vialattea.net\/content\/2651\/","title":{"rendered":"Io vorrei sapere la reazione chimica completa che porta alla formazione de DDT? E&#8217; possibile averla? Mi servirebbe per gli esami di stato e non riesco a trovarla da nessuna parte&#8230;.Grazie mille ciao ciao"},"content":{"rendered":"<p>Riportiamo innanzitutto alcuni dettagli di interesse chimico sul DDT (dicloro-difenil-tricloroetano) CASRN: <strong>50-29-3 <br \/><\/strong><strong>Molecular Formula:<\/strong>\u00a0 C14-H9-Cl5 ([The Merck Index. 10th ed. Rahway, New Jersey: Merck Co., Inc., 1983., p. 409<br \/><strong>Molecular Weight:<\/strong> 354.49 <br \/><strong>Boiling point:<\/strong> 260\u00b0C<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" style=\"WIDTH: 289px; HEIGHT: 157px\" height=\"157\" alt=\"\" src=\"http:\/\/www.vialattea.net\/spaw\/image\/ambiente\/DDT.png\" width=\"289\"\/><\/p>\n<p>Struttura molecolare del DDT (Tratta da <a href=\"http:\/\/www.wikipedia.org\">www.wikipedia.org<\/a>)<\/p>\n<p><strong>Density\/Specific Gravity:<\/strong> 0.98 to 0.99 <br \/>[Clayton, G.D., F.E. Clayton (eds.) Patty\u2019s Industrial Hygiene and Toxicology. Volumes 2A, 2B, 2C, 2D, 2E, 2F: Toxicology. 4th ed. New York, NY: John Wiley &amp; Sons Inc., 1993-1994., p. 1508]**PEER REVIEWED** <br \/><strong>Octanol\/Water Partition Coefficient:<\/strong> <br \/>log Kow = 6.91\u00a0 [Hansch, C., Leo, A., D. Hoekman. Exploring QSAR &#8211; Hydrophobic, Electronic, and Steric Constants. Washington, DC: American Chemical Society., 1995., p. 118]**PEER REVIEWED** <\/p>\n<p><strong>Spectral Properties:<\/strong> <br \/>Max absorption (95% alcohol): 236 nm <br \/>[Budavari, S. (ed.). The Merck Index &#8211; An Encyclopedia of Chemicals, Drugs, and Biologicals. Whitehouse Station, NJ: Merck and Co., Inc., 1996., p. 481]**PEER REVIEWED** <br \/>IR: 15542 (Sadtler Research Laboratories Prism Collection) <br \/>[Weast, R.C. and M.J. Astle. CRC Handbook of Data on Organic Compounds. Volumes I and II. Boca Raton, FL: CRC Press Inc. 1985., p. V1 601]**PEER REVIEWED** <br \/>UV: 4655 (Sadtler Research Laboratories Spectral Collection) <br \/>[Weast, R.C. and M.J. Astle. CRC Handbook of Data on Organic Compounds. Volumes I and II. Boca Raton, FL: CRC Press Inc. 1985., p. V1 601]**PEER REVIEWED** <br \/>NMR: 620 (Varian Associates NMR Spectra Catalogue) <br \/>[Weast, R.C. and M.J. Astle. CRC Handbook of Data on Organic Compounds. Volumes I and II. Boca Raton, FL: CRC Press Inc. 1985., p. V1 601]**PEER REVIEWED** <br \/>Intensity of mass spectral peaks: 246 M\/z (100%); 318 M\/z (79%); 248 M\/z (66%); 316 M\/z (61%) <br \/>[Hites, R.A. Handbook of Mass Spectra of Environmental Contaminants. Boca Raton, FL: CRC Press Inc., 1985., p. 105]**PEER REVIEWED** <\/p>\n<p><strong>Vapor Pressure: <br \/><\/strong>1.6X10-7 mm Hg @ 20 deg C\u00a0 [Bidleman TF, Foreman WT; Adv Chem Ser 216:27-56 (1987)]**PEER REVIEWED** <\/p>\n<p>Alcune interessanti <strong>informazioni storiche<\/strong> si possono torvare al link di seguito a cui rimando:<\/p>\n<p><a href=\"http:\/\/www.anisn.it\/scuola\/strumenti\/licheni\/ddt.htm\">http:\/\/www.anisn.it\/scuola\/strumenti\/licheni\/ddt.htm<\/a><\/p>\n<p><strong>Per la fabbricazione: <\/strong><\/p>\n<p>Indichiamo di sseguito due riferimenti bilgiografici per la fabbricazione che possono essere rintracciati nelle biblioteca di chimica tramite il C.A.S. che sar\u00e0 sicuramente disponibile, sopratatutto si consiglia di consultare l&#8217;ottimo e sempre presente KIRK-Othmer.<\/p>\n<p>1) Chlorobenzene undergoes acid-catalyzed condensation with trichloroacetaldehyde to produce DDT. <br \/>[Kirk-Othmer Encyclopedia of Chemical Technology. 3rd ed., Volumes 1-26. New York, NY: John Wiley and Sons, 1978-1984., p. 5(79) 800]**PEER REVIEWED** <\/p>\n<p>2)&#8230; P Muller, US patent 2,329,074 (1944 to Geigy). &#8230; large scale production. <br \/>[Budavari, S. (ed.). The Merck Index &#8211; An Encyclopedia of Chemicals, Drugs, and Biologicals. Whitehouse Station, NJ: Merck and Co., Inc., 1996., p. 481]**PEER REVIEWED** <\/p>\n<p\/>\n","protected":false},"excerpt":{"rendered":"<p>[&#8230;]<\/p>\n","protected":false},"author":166,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[25],"tags":[],"class_list":["post-2651","post","type-post","status-publish","format-standard","hentry","category-inquinamento"],"_links":{"self":[{"href":"https:\/\/www.vialattea.net\/content\/wp-json\/wp\/v2\/posts\/2651","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.vialattea.net\/content\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.vialattea.net\/content\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.vialattea.net\/content\/wp-json\/wp\/v2\/users\/166"}],"replies":[{"embeddable":true,"href":"https:\/\/www.vialattea.net\/content\/wp-json\/wp\/v2\/comments?post=2651"}],"version-history":[{"count":0,"href":"https:\/\/www.vialattea.net\/content\/wp-json\/wp\/v2\/posts\/2651\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.vialattea.net\/content\/wp-json\/wp\/v2\/media?parent=2651"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.vialattea.net\/content\/wp-json\/wp\/v2\/categories?post=2651"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.vialattea.net\/content\/wp-json\/wp\/v2\/tags?post=2651"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}