{"id":126154,"date":"2024-05-19T15:51:10","date_gmt":"2024-05-19T12:51:10","guid":{"rendered":"https:\/\/milliycha.uz\/?p=126154"},"modified":"2024-05-19T15:51:23","modified_gmt":"2024-05-19T12:51:23","slug":"stereokimyo","status":"publish","type":"post","link":"https:\/\/milliycha.uz\/ru\/stereokimyo\/","title":{"rendered":"Stereokimyo"},"content":{"rendered":"\n<p>Stereokimyo (Stereo &#8230; va kimyo) \u2014 kimyoning molekuladagi atom yoki atomlar guruhi (radikallar)ning fazo- viy joylashishini o&#8217;rganadigan sohasi. S. dastlab 19-a. oxirlarida ya.G. Vant- Goff tadqiqotlari asosida organik ki- myoning bo&#8217;limi sifatida paydo bo&#8217;ldi. S. geometrik (yoki tsistrans) va optic izomeriyanp o&#8217;rganadi. Geometrik izo- meriya, asosan, molekulasi tuzilishida qo&#8217;shbog&#8217;yoki tsiklik bog&#8217;langan atomlari bo&#8217;lgan birikmalarga xosdir. Geometrik izomeriyaga o&#8217;xshash aylanma izomeriya aromatik birikmalarda uchraydi. Mas, 2,2&#8217;dinitrofenil \u2014 6,6&#8242; dikarbon kis- lota qutbli guruhlarning o&#8217;zaro ta&#8217;siri natijasida ular bog&#8217;i o&#8217;q atrofida ayla- nishiga to&#8217;sqinlik qiladi. Shu boisdan bu birikmaning 2 ta fazoviy shakli (I va II shakllar) mavjud. Organik moddalarda, jumladan, tabi- iy birikmalarda (saxaridlar, oqsillar, alkaloidlar) optik izomeriya hodisasi ham keng o&#8217;rinni egallaydi. Izomeriya- ning bu turida molekuladagi asimmetrik atomuglerod 4 valent bog&#8217;ining har biri turli o&#8217;rinbosarlar (atom va radikal- lar) bilan bog&#8217;langan bo&#8217;ladi. Bunday bi- rikmalar, mas, sut kislota SN3SN(on) Soon, optik faol, ya&#8217;ni yorug&#8217;lik nu- rining qutblanish tekisligini burish xususiyatiga ega va shu sababli 2 shaklda (optik antipodlar) mavjud bo&#8217;la oladi. Optik izomeriyani ba&#8217;zan kuzgu izo- meriya deb ham ataladi, chunki fazoviy izomerlar go&#8217;yo predmetning ko&#8217;zgudagi aksini eslatadi. Asimmetrik atom sifa- tida azot, oltingugurt, kremniy, fosfor va b. atomlar bo&#8217;lgan birikmalardagi izomeriya hodisasi xam o&#8217;rganilgan. S. organik kimyodan tashqari anorganik ko- ordinasiey birikmalarni ham o&#8217;rganadi, qattiq jismlar nazariyasi va kristallar kimyosiga yondashib tadqiqotlar o&#8217;tkazadi. S. polimerlar, dorivor moddalar va b. faol muhim ahamiyatga ega. Ad.: Potapov . M ., Stereoximiya, M., 1988;Parpiev N. A., Rahimov H.R., Muftahov A. ., Umumiy kimyoning naza- riy asoslari. T., 2004. Kudrat Axmerov.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Stereokimyo (Stereo &#8230; va kimyo) \u2014 kimyoning molekuladagi atom yoki atomlar guruhi (radikallar)ning fazo- viy joylashishini o&#8217;rganadigan sohasi. S. dastlab 19-a. oxirlarida ya.G. Vant- Goff tadqiqotlari asosida organik ki- myoning &hellip; <a href=\"https:\/\/milliycha.uz\/ru\/stereokimyo\/\" 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":[206],"tags":[],"class_list":["post-126154","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-s-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\/126154","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=126154"}],"version-history":[{"count":1,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/posts\/126154\/revisions"}],"predecessor-version":[{"id":126172,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/posts\/126154\/revisions\/126172"}],"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=126154"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/categories?post=126154"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/milliycha.uz\/ru\/wp-json\/wp\/v2\/tags?post=126154"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}