{"id":116546,"date":"2024-02-29T10:53:25","date_gmt":"2024-02-29T07:53:25","guid":{"rendered":"https:\/\/milliycha.uz\/?p=116546"},"modified":"2024-02-29T10:53:28","modified_gmt":"2024-02-29T07:53:28","slug":"izonitrillar","status":"publish","type":"post","link":"https:\/\/milliycha.uz\/ru\/izonitrillar\/","title":{"rendered":"Izonitrillar"},"content":{"rendered":"\n<p>Izonitrillar (izosianidlar, karbilaminlar) \u2014 umumiy formulasi RNC (bu yerda R \u2014 organik radikal) bo&#8217;lgan organik birikmalar, tsianid kislota hosilalari, nitrillar izomerlarining Izonitrillar nitrillaridan farqi shuki, ularda CN guruhi organik radikal bilan azot orqali bog&#8217;langan: R\u2014NsC; nitrillarda esa organik radikal bu guruh bilan uglerod orqali bog&#8217;langan bo&#8217;lib, R\u2014 C=N tartibida joylashgan. Galogenalkillar bilan kumush tsianidning o&#8217;zaro almashinishidan va boshqa yo&#8217;llar bilan olinadi. Masalan, CH3I+AgCN->CH,NC+AgI. Oddiy Izonitrillar qo&#8217;lansa hid chiqarib, tubidan qaynaydigan suyuqliklardir. Izonitrillar mineral kislotalarning suvdagi eritmasida gidrolizlanib, birlamchi aminlar va chumoli kislota hosil qiladi. Izonitrillar organik sintezda muhim oraliq mahsulot bo&#8217;lib, turli geterosiklik birikmalar, peptidlar va boshqalar olishda, birlamchi aminlarning sifat analizida qo&#8217;llaniladi.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Izonitrillar (izosianidlar, karbilaminlar) \u2014 umumiy formulasi RNC (bu yerda R \u2014 organik radikal) bo&#8217;lgan organik birikmalar, tsianid kislota hosilalari, nitrillar izomerlarining Izonitrillar nitrillaridan farqi shuki, ularda CN guruhi organik radikal &hellip; <a href=\"https:\/\/milliycha.uz\/ru\/izonitrillar\/\" 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":[199],"tags":[],"class_list":["post-116546","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-i-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\/116546","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=116546"}],"version-history":[{"count":1,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/posts\/116546\/revisions"}],"predecessor-version":[{"id":116550,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/posts\/116546\/revisions\/116550"}],"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=116546"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/categories?post=116546"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/tags?post=116546"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}