{"id":20256,"date":"2022-03-05T17:34:46","date_gmt":"2022-03-05T14:34:46","guid":{"rendered":"https:\/\/milliycha.uz\/?p=20256"},"modified":"2022-03-05T17:34:46","modified_gmt":"2022-03-05T14:34:46","slug":"butil-spirtlar","status":"publish","type":"post","link":"https:\/\/milliycha.uz\/kr\/butil-spirtlar\/","title":{"rendered":"BUTIL SPIRTLAR"},"content":{"rendered":"\n<p>BUTIL SPIRTLAR, butanollar, S4N, on \u2014 bir atomli spirtlar. Molekulyar modda 74,12. Rangsiz suyuqlik, o&#8217;ziga xos hidi bor. To&#8217;rtta izomeri ma&#8217;lum: birlamchi (butanol1) SN3SN2SN2SN2ON, ikkilamchi (butanol2) SN3SN2SNONSN3, izobutil (2metilpropanol1) (SN3)2 SNSN2ON, uchlamchi (uch metilkarbinol) (SN3)3SON. Butanol1 bilan butanol2 da uglerod atomlarining tarmoqlanmagan zanjirlari bor. Izobutil Butil spirtlarda asimmetrik uglerod atomi bo&#8217;lganligi sababli uch shaklda mavjud: ulardan ikkitasi optik faol, uchinchisi ratsemik (inaktiv) shakldir. Butil spirtlar etil spirt va efir bilan yaxshi aralashadi, spirtlarga xos hamma reaktsiyalarga kirishadi, uglevodlarni bijg&#8217;itish yo&#8217;li bilan, shuningdek sintetik usulda olinadi. Loklar, tsellyuloza, smolalar ishlab chiqarishda erituvchi sifatida, yuvish vositalarini sintez qilishda ishlatiladi.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>BUTIL SPIRTLAR, butanollar, S4N, on \u2014 bir atomli spirtlar. Molekulyar modda 74,12. Rangsiz suyuqlik, o&#8217;ziga xos hidi bor. To&#8217;rtta izomeri ma&#8217;lum: birlamchi (butanol1) SN3SN2SN2SN2ON, ikkilamchi (butanol2) SN3SN2SNONSN3, izobutil (2metilpropanol1) (SN3)2 &hellip; <a href=\"https:\/\/milliycha.uz\/kr\/butil-spirtlar\/\" class=\"more-link\">Read More<\/a><\/p>\n","protected":false},"author":1,"featured_media":16402,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[114],"tags":[],"class_list":["post-20256","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-b-harfi","entry"],"translation":{"provider":"WPGlobus","version":"3.0.2","language":"kr","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\/kr\/wp-json\/wp\/v2\/posts\/20256","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/milliycha.uz\/kr\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/milliycha.uz\/kr\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/milliycha.uz\/kr\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/milliycha.uz\/kr\/wp-json\/wp\/v2\/comments?post=20256"}],"version-history":[{"count":1,"href":"https:\/\/milliycha.uz\/kr\/wp-json\/wp\/v2\/posts\/20256\/revisions"}],"predecessor-version":[{"id":20262,"href":"https:\/\/milliycha.uz\/kr\/wp-json\/wp\/v2\/posts\/20256\/revisions\/20262"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/milliycha.uz\/kr\/wp-json\/wp\/v2\/media\/16402"}],"wp:attachment":[{"href":"https:\/\/milliycha.uz\/kr\/wp-json\/wp\/v2\/media?parent=20256"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/milliycha.uz\/kr\/wp-json\/wp\/v2\/categories?post=20256"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/milliycha.uz\/kr\/wp-json\/wp\/v2\/tags?post=20256"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}