{"id":122424,"date":"2024-05-12T16:06:24","date_gmt":"2024-05-12T13:06:24","guid":{"rendered":"https:\/\/milliycha.uz\/?p=122424"},"modified":"2024-05-12T16:06:28","modified_gmt":"2024-05-12T13:06:28","slug":"merkaptanlar","status":"publish","type":"post","link":"https:\/\/milliycha.uz\/ru\/merkaptanlar\/","title":{"rendered":"Merkaptanlar"},"content":{"rendered":"\n<p>Merkaptanlar (tiollar) &#8212; vodo- rod sulfidning organik hosilalari. Umumiy formulasi RSH, bu erda R\u2014 uglevodorod radikali, M.ning metil- merkaptan (SN3\u2014SH), etilmerkap- tan (S5N5\u2014SH) va b. turlari bor. M. qo&#8217;lansa hidli, gazsimon, suyuq va qattiq moddalar. Suvda yomon, organic erituvchilarda yaxshi eriydi. M. tabi- atda oqsillarning chirishidan hosil bo&#8217;ladigan mahsulotlarda uchraydi. M. merkaptid tuzlarini hosil qiladi, mas, simob merkaptid (RS)2 Hg (M.ning nomi shundan olingan, lot. mercurum captaus \u2014 bog&#8217;lovchi simob). M. va hosilalari (tuzlari, sulfidlari va disulfidla- ri) tabiiy va sintetik kauchuklarni vul- kanizasiyalashda, ba&#8217;zi dorivor modda- lar va insektisidlarni sintez qilishda qo&#8217;llanadi. To&#8217;yingan uglevodlarning ga- logenli hosilalariga natriy yoki kaliy gidrosulfid ta&#8217;sir ettirib olinadi.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Merkaptanlar (tiollar) &#8212; vodo- rod sulfidning organik hosilalari. Umumiy formulasi RSH, bu erda R\u2014 uglevodorod radikali, M.ning metil- merkaptan (SN3\u2014SH), etilmerkap- tan (S5N5\u2014SH) va b. turlari bor. M. qo&#8217;lansa hidli, &hellip; <a href=\"https:\/\/milliycha.uz\/ru\/merkaptanlar\/\" class=\"more-link\">Read More<\/a><\/p>\n","protected":false},"author":1,"featured_media":99837,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[217],"tags":[],"class_list":["post-122424","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-m-harfi","entry"],"translation":{"provider":"WPGlobus","version":"3.0.2","language":"ru","enabled_languages":["uz","kr","ru"],"languages":{"uz":{"title":true,"content":true,"excerpt":false},"kr":{"title":false,"content":false,"excerpt":false},"ru":{"title":false,"content":false,"excerpt":false}}},"_links":{"self":[{"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/posts\/122424","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/comments?post=122424"}],"version-history":[{"count":1,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/posts\/122424\/revisions"}],"predecessor-version":[{"id":122439,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/posts\/122424\/revisions\/122439"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/media\/99837"}],"wp:attachment":[{"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/media?parent=122424"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/categories?post=122424"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/tags?post=122424"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}