{"id":843,"date":"2023-07-20T21:13:35","date_gmt":"2023-07-20T21:13:35","guid":{"rendered":"https:\/\/chemuza.org\/tr\/sikloheksen-c6h10\/"},"modified":"2023-07-20T21:13:35","modified_gmt":"2023-07-20T21:13:35","slug":"sikloheksen-c6h10","status":"publish","type":"post","link":"https:\/\/chemuza.org\/tr\/sikloheksen-c6h10\/","title":{"rendered":"Sikloheksen &#8211; c6h10, 110-83-8"},"content":{"rendered":"<p>Sikloheksen (C6H10), reaktivitesi ve \u00e7ok y\u00f6nl\u00fcl\u00fc\u011f\u00fc nedeniyle kimyasal reaksiyonlarda yayg\u0131n olarak bir \u00e7\u00f6z\u00fcc\u00fc ve ara madde olarak kullan\u0131lan siklik \u00e7ift ba\u011fl\u0131 bir hidrokarbondur.<\/p>\n<figure class=\"wp-block-table\">\n<table>\n<tbody>\n<tr>\n<td> IUPAC Ad\u0131<\/td>\n<td> sikloheksen<\/td>\n<\/tr>\n<tr>\n<td> Molek\u00fcler form\u00fcl<\/td>\n<td> C\u2086H\u2081\u2080<\/td>\n<\/tr>\n<tr>\n<td> CAS numaras\u0131<\/td>\n<td> 110-83-8<\/td>\n<\/tr>\n<tr>\n<td> E\u015f anlaml\u0131<\/td>\n<td> Monosikloheksen, Heksanaften, 1,2-dihidrobenzen<\/td>\n<\/tr>\n<tr>\n<td> InChI<\/td>\n<td> InChI=1S\/C6H10\/c1-2-4-6-5-3-1\/h1-2H,3-6H2<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/figure>\n<h2 class=\"wp-block-heading\"> <strong>Sikloheksenin \u00f6zellikleri<\/strong><\/h2>\n<h3 class=\"wp-block-heading\"> Sikloheksen Form\u00fcl\u00fc<\/h3>\n<p> Sikloheksenin form\u00fcl\u00fc, molek\u00fcler bile\u015fimini temsil eden C\u2086H\u2081\u2080&#8217;dir. Her bir karbon atomunun iki hidrojen atomuna ba\u011fl\u0131 oldu\u011fu, bir halka halinde d\u00fczenlenmi\u015f alt\u0131 karbon atomundan olu\u015fur. Bu d\u00f6ng\u00fcsel yap\u0131, siklohekzen&#8217;e benzersiz \u00f6zelliklerini ve reaktivitesini verir.<\/p>\n<h3 class=\"wp-block-heading\"> Sikloheksen Molar K\u00fctlesi<\/h3>\n<p> Monosikloheksenin molar k\u00fctlesi, onu olu\u015fturan elementlerin atomik k\u00fctleleri toplanarak hesaplanabilir. Alt\u0131 karbon atomunun (her biri 12,01 g\/mol) ve on hidrojen atomunun (her biri 1,008 g\/mol) atomik k\u00fctlelerinin eklenmesiyle belirlenir. Dolay\u0131s\u0131yla monosikloheksenin molar k\u00fctlesi yakla\u015f\u0131k 82,14 g\/mol&#8217;d\u00fcr.<\/p>\n<h3 class=\"wp-block-heading\"> Sikloheksenin kaynama noktas\u0131<\/h3>\n<p> Monosikloheksen, 83-85\u00b0C (181-185\u00b0F) civar\u0131nda nispeten d\u00fc\u015f\u00fck bir kaynama noktas\u0131na sahiptir. Bu d\u00fc\u015f\u00fck kaynama noktas\u0131, onu bir solvent veya reaksiyon ara maddesi olarak \u00e7e\u015fitli uygulamalar i\u00e7in uygun hale getirir. Nispeten d\u00fc\u015f\u00fck kaynama noktas\u0131, \u00e7e\u015fitli end\u00fcstriyel i\u015flemler s\u0131ras\u0131nda monosikloheksenin kolay ayr\u0131lmas\u0131n\u0131 ve geri kazan\u0131lmas\u0131n\u0131 sa\u011flar.<\/p>\n<h3 class=\"wp-block-heading\"> Sikloheksen Erime Noktas\u0131<\/h3>\n<p> Monosikloheksenin erime noktas\u0131 yakla\u015f\u0131k -104 ila -103\u00b0C&#8217;dir (-155 ila -153\u00b0F). Bu d\u00fc\u015f\u00fck erime noktas\u0131, monosikloheksenin oda s\u0131cakl\u0131\u011f\u0131nda s\u0131v\u0131 halde bulunmas\u0131na izin verir ve onun \u00e7ok \u00e7e\u015fitli kimyasal reaksiyonlarda ve i\u015flemlerde bir reaktif veya solvent olarak kullan\u0131lmas\u0131n\u0131 kolayla\u015ft\u0131r\u0131r.<\/p>\n<h3 class=\"wp-block-heading\"> Sikloheksen yo\u011funlu\u011fu g\/mL<\/h3>\n<p> Monosikloheksenin oda s\u0131cakl\u0131\u011f\u0131nda yakla\u015f\u0131k 0,81 ila 0,83 g\/mL yo\u011funlu\u011fu vard\u0131r. Bu yo\u011funluk de\u011feri, monosikloheksenin sudan daha az yo\u011fun oldu\u011funu ve su y\u00fczeyinde y\u00fczmesini sa\u011flad\u0131\u011f\u0131n\u0131 g\u00f6sterir. Monosikloheksenin yo\u011funlu\u011fu, \u00e7e\u015fitli end\u00fcstriyel ve laboratuvar uygulamalar\u0131nda davran\u0131\u015f\u0131n\u0131n belirlenmesinde \u00e7ok \u00f6nemli bir rol oynar.<\/p>\n<h3 class=\"wp-block-heading\"> Sikloheksen Molek\u00fcl A\u011f\u0131rl\u0131\u011f\u0131<\/h3>\n<p> Bir molek\u00fcldeki t\u00fcm atomlar\u0131n atom a\u011f\u0131rl\u0131klar\u0131n\u0131n toplam\u0131 olan monosikloheksenin molek\u00fcler a\u011f\u0131rl\u0131\u011f\u0131 yakla\u015f\u0131k 82,14 g\/mol&#8217;d\u00fcr. Bu molek\u00fcler a\u011f\u0131rl\u0131k de\u011feri stokiyometrinin hesaplanmas\u0131, reaktan miktarlar\u0131n\u0131n belirlenmesi ve monosikloheksenin fiziksel ve kimyasal \u00f6zelliklerinin anla\u015f\u0131lmas\u0131 i\u00e7in gereklidir. <\/p>\n<div class=\"wp-block-image\">\n<figure class=\"alignright size-large is-resized\"><img decoding=\"async\" loading=\"lazy\" src=\"https:\/\/chemuza.org\/wp-content\/uploads\/2023\/08\/cyclohexene.jpg\" alt=\"sikloheksen\" width=\"143\" height=\"143\" srcset=\"\" sizes=\"\"><\/figure>\n<\/div>\n<h3 class=\"wp-block-heading\"> Sikloheksenin yap\u0131s\u0131<\/h3>\n<p> Monosikloheksen, iki biti\u015fik karbon atomu aras\u0131nda \u00e7ift ba\u011f bulunan alt\u0131 \u00fcyeli bir karbon halkas\u0131yla karakterize edilen benzersiz bir molek\u00fcler yap\u0131ya sahiptir. Bu yap\u0131, monosikloheksen&#8217;e hem stabilite hem de reaktivite kazand\u0131r\u0131r, bu da onu \u00e7e\u015fitli kimyasal reaksiyonlarda ve organik sentezlerde \u00e7ok y\u00f6nl\u00fc bir bile\u015fik haline getirir.<\/p>\n<h3 class=\"wp-block-heading\"> Sikloheksenin \u00e7\u00f6z\u00fcn\u00fcrl\u00fc\u011f\u00fc<\/h3>\n<p> Monosikloheksenin polar olmayan yap\u0131s\u0131ndan dolay\u0131 suda \u00e7\u00f6z\u00fcn\u00fcrl\u00fc\u011f\u00fc s\u0131n\u0131rl\u0131d\u0131r. Ancak etanol, aseton ve eter gibi organik \u00e7\u00f6z\u00fcc\u00fclerde \u00e7ok \u00e7\u00f6z\u00fcn\u00fcr. Bu \u00e7\u00f6z\u00fcn\u00fcrl\u00fck davran\u0131\u015f\u0131, monosikloheksenin organik \u00e7\u00f6z\u00fcc\u00fcler i\u00e7inde kolayca kar\u0131\u015ft\u0131r\u0131lmas\u0131na ve \u00e7\u00f6z\u00fcnmesine olanak tan\u0131r, b\u00f6ylece \u00e7e\u015fitli i\u015flemlerde bir reaktif veya \u00e7\u00f6z\u00fcc\u00fc olarak uygulanmas\u0131 geli\u015ftirilir.<\/p>\n<figure class=\"wp-block-table\">\n<table>\n<tbody>\n<tr>\n<td> D\u0131\u015f g\u00f6r\u00fcn\u00fc\u015f<\/td>\n<td> Renksiz<\/td>\n<\/tr>\n<tr>\n<td> Spesifik yer \u00e7ekimi<\/td>\n<td> 0.81-0.83<\/td>\n<\/tr>\n<tr>\n<td> Renk<\/td>\n<td> Renksiz<\/td>\n<\/tr>\n<tr>\n<td> Koku<\/td>\n<td> Eter gibi yumu\u015fak<\/td>\n<\/tr>\n<tr>\n<td> Molar k\u00fctle<\/td>\n<td> 82,14 gr\/mol<\/td>\n<\/tr>\n<tr>\n<td> Yo\u011funluk<\/td>\n<td> 0,81-0,83 g\/mL<\/td>\n<\/tr>\n<tr>\n<td> F\u00fczyon noktas\u0131<\/td>\n<td> -104 ila -103\u00b0C<\/td>\n<\/tr>\n<tr>\n<td> Kaynama noktas\u0131<\/td>\n<td> 83-85\u00b0C<\/td>\n<\/tr>\n<tr>\n<td> Fla\u015f noktas\u0131<\/td>\n<td> -7\u00b0C<\/td>\n<\/tr>\n<tr>\n<td> sudaki \u00e7\u00f6z\u00fcn\u00fcrl\u00fck<\/td>\n<td> \u00c7\u00f6z\u00fcnmez<\/td>\n<\/tr>\n<tr>\n<td> \u00e7\u00f6z\u00fcn\u00fcrl\u00fck<\/td>\n<td> Organik \u00e7\u00f6z\u00fcc\u00fclerde \u00e7\u00f6z\u00fcn\u00fcr<\/td>\n<\/tr>\n<tr>\n<td> Buhar bas\u0131nc\u0131<\/td>\n<td> 184 mmHg<\/td>\n<\/tr>\n<tr>\n<td> Buhar yo\u011funlu\u011fu<\/td>\n<td> 2,9 (hava = 1)<\/td>\n<\/tr>\n<tr>\n<td> pKa<\/td>\n<td> ~15.5<\/td>\n<\/tr>\n<tr>\n<td> pH<\/td>\n<td> Uygulanamaz<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/figure>\n<h2 class=\"wp-block-heading\"> <strong>Sikloheksenin g\u00fcvenli\u011fi ve tehlikeleri<\/strong><\/h2>\n<p> Monosikloheksen baz\u0131 g\u00fcvenlik riskleri ta\u015f\u0131r ve kullan\u0131l\u0131rken dikkatli olunmal\u0131d\u0131r. Yan\u0131c\u0131d\u0131r ve d\u00fc\u015f\u00fck s\u0131cakl\u0131klarda tutu\u015fabilir. Monosikloheksen ile \u00e7al\u0131\u015f\u0131rken buhar olu\u015fumunu \u00f6nlemek i\u00e7in yeterli havaland\u0131rman\u0131n sa\u011flanmas\u0131 \u00f6nemlidir. Ciltte, g\u00f6zlerde ve solunum sisteminde tahri\u015fe neden olabilece\u011finden s\u0131v\u0131 veya buharla do\u011frudan temastan ka\u00e7\u0131n\u0131lmal\u0131d\u0131r. Uzun s\u00fcreli veya tekrarlanan maruz kalma, olumsuz sa\u011fl\u0131k etkilerine neden olabilir. Yutulmas\u0131 veya solunmas\u0131 halinde derhal t\u0131bbi m\u00fcdahale gereklidir. Monosikloheksen ile ili\u015fkili potansiyel riskleri en aza indirmek i\u00e7in uygun ki\u015fisel koruyucu ekipman\u0131n kullan\u0131m\u0131 da dahil olmak \u00fczere uygun depolama ve ta\u015f\u0131ma prosed\u00fcrlerinin takip edilmesi \u00f6nemlidir.<\/p>\n<figure class=\"wp-block-table\">\n<table>\n<tbody>\n<tr>\n<td> Tehlike sembolleri<\/td>\n<td> XI<\/td>\n<\/tr>\n<tr>\n<td> G\u00fcvenlik A\u00e7\u0131klamas\u0131<\/td>\n<td> Cilt ve g\u00f6z tahri\u015fine neden olabilir. Yan\u0131c\u0131 s\u0131v\u0131 ve buhar.<\/td>\n<\/tr>\n<tr>\n<td> BM kimlik numaralar\u0131<\/td>\n<td> UN 2256, UN 2257<\/td>\n<\/tr>\n<tr>\n<td> HS kodu<\/td>\n<td> 2902.19.0000<\/td>\n<\/tr>\n<tr>\n<td> Tehlike s\u0131n\u0131f\u0131<\/td>\n<td> 3 (Yan\u0131c\u0131 s\u0131v\u0131)<\/td>\n<\/tr>\n<tr>\n<td> Paketleme grubu<\/td>\n<td> III (D\u00fc\u015f\u00fck tehlike)<\/td>\n<\/tr>\n<tr>\n<td> Toksisite<\/td>\n<td> Uzun s\u00fcreli veya tekrarl\u0131 maruz kalma sonucu sa\u011fl\u0131k \u00fczerinde olumsuz etkilere neden olabilir.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/figure>\n<h2 class=\"wp-block-heading\"> <strong>Sikloheksen sentez y\u00f6ntemleri<\/strong><\/h2>\n<p> Monosiklohekseni \u00e7e\u015fitli y\u00f6ntemler sentezleyebilir.<\/p>\n<p> Yayg\u0131n bir y\u00f6ntem, bak\u0131r veya platin gibi bir kataliz\u00f6r\u00fcn kullan\u0131m\u0131n\u0131 i\u00e7eren <a href=\"https:\/\/chemuza.org\/tr\/sikloheksanol\/\">sikloheksanol\u00fcn<\/a> katalitik dehidrojenasyonudur. Kataliz\u00f6r, siklohekzanol\u00fcn y\u00fcksek s\u0131cakl\u0131klarda \u0131s\u0131t\u0131lmas\u0131 s\u0131ras\u0131nda hidrojen atomlar\u0131n\u0131n uzakla\u015ft\u0131r\u0131lmas\u0131n\u0131 kolayla\u015ft\u0131r\u0131r, bu da monosikloheksen olu\u015fumuna neden olur.<\/p>\n<p> Ba\u015fka bir y\u00f6ntem, <a href=\"https:\/\/chemuza.org\/tr\/sikloheksanol\/\">sikloheksanol\u00fcn<\/a> s\u00fclf\u00fcrik asit veya fosforik asit gibi g\u00fc\u00e7l\u00fc bir asitle eliminasyon reaksiyonudur. Asit kataliz\u00f6r\u00fc, bir su molek\u00fcl\u00fcn\u00fcn sikloheksanolden uzakla\u015ft\u0131r\u0131lmas\u0131n\u0131 te\u015fvik ederek monosikloheksen olu\u015fumuna yol a\u00e7ar.<\/p>\n<p> Ek olarak <a href=\"https:\/\/chemuza.org\/tr\/sikloheksanol\/\">sikloheksanol<\/a> veya sikloheksilaminin pirolizi monosikloheksen verir. Piroliz, ba\u015flang\u0131\u00e7 malzemesinin oksijen yoklu\u011funda y\u00fcksek s\u0131cakl\u0131klara maruz b\u0131rak\u0131lmas\u0131n\u0131, molek\u00fcler ba\u011flar\u0131n k\u0131r\u0131lmas\u0131na ve monosikloheksenin olu\u015fmas\u0131na neden olmay\u0131 i\u00e7erir.<\/p>\n<p> Krom trioksit veya potasyum permanganat gibi oksitleyici maddeler, monosiklohekseni sentezlemek i\u00e7in <a href=\"https:\/\/chemuza.org\/tr\/sikloheksan-c6h12\/\">sikloheksan\u0131<\/a> oksitler. Bu oksidasyon reaksiyonu, karbon halkas\u0131na bir \u00e7ift ba\u011f ekleyerek <a href=\"https:\/\/chemuza.org\/tr\/sikloheksan-c6h12\/\">sikloheksan\u0131<\/a> monosiklohekzene d\u00f6n\u00fc\u015ft\u00fcr\u00fcr.<\/p>\n<p> Bu y\u00f6ntemlerin her biri, sentezin \u00f6zel gereksinimlerine ba\u011fl\u0131 olarak farkl\u0131 avantajlar sunar. Monosikloheksen sentezinde y\u00fcksek verim ve istenen \u00fcr\u00fcn safl\u0131\u011f\u0131n\u0131 elde etmek i\u00e7in reaksiyon ko\u015fullar\u0131, kataliz\u00f6rler ve safla\u015ft\u0131rma teknikleri dikkatle de\u011ferlendirilmelidir.<\/p>\n<h2 class=\"wp-block-heading\"> <strong>Sikloheksenin kullan\u0131m alanlar\u0131<\/strong><\/h2>\n<p> Monosikloheksen, benzersiz \u00f6zellikleri ve reaktivitesinden dolay\u0131 \u00e7e\u015fitli uygulamalar bulur. Monosikloheksenin baz\u0131 \u00f6nemli kullan\u0131mlar\u0131 \u015funlard\u0131r:<\/p>\n<ul>\n<li> \u00c7\u00f6z\u00fcc\u00fc: Monosikloheksen, bir\u00e7ok kimyasal reaksiyonda, \u00f6zellikle de polar olmayan veya hafif polar bile\u015fikleri i\u00e7erenlerde \u00e7ok y\u00f6nl\u00fc bir \u00e7\u00f6z\u00fcc\u00fc olarak hizmet eder. Genellikle ya\u011flar\u0131, re\u00e7ineleri, mumlar\u0131 ve di\u011fer organik maddeleri \u00e7\u00f6zer.<\/li>\n<li> Kimyasal sentezde ara madde: Monosikloheksen, naylon \u00fcretiminde kullan\u0131lan \u00f6nemli bir bile\u015fen olan adipik asit de dahil olmak \u00fczere \u00e7e\u015fitli kimyasallar\u0131n sentezinde bir ara madde olarak \u00e7ok \u00f6nemli bir rol oynar. Ayn\u0131 zamanda sikloheksanol ve sikloheksanonun sentezi i\u00e7in bir \u00f6nc\u00fc g\u00f6revi g\u00f6r\u00fcr.<\/li>\n<li> Polimerizasyon: Kaplamalarda, yap\u0131\u015ft\u0131r\u0131c\u0131larda ve elastomerlerde kullan\u0131lan bir polimer olan poli(monosikloheksen), \u00fcretiminde monomer olarak monosikloheksen kullan\u0131r.<\/li>\n<li> Organik reaksiyonlar: Monosikloheksen, siklokat\u0131lmalar, oksidasyon ve indirgeme reaksiyonlar\u0131 gibi \u00e7ok \u00e7e\u015fitli organik reaksiyonlara kat\u0131l\u0131r. Siklik bile\u015fiklerin olu\u015fumunda ve farmas\u00f6tiklerin, parf\u00fcmlerin ve aromalar\u0131n sentezinde bir reaktif olarak \u00f6zellikle faydal\u0131d\u0131r.<\/li>\n<li> Ekstraksiyon ve safla\u015ft\u0131rma: Bitki \u00f6zleri, u\u00e7ucu ya\u011flar ve aromalar dahil olmak \u00fczere do\u011fal \u00fcr\u00fcnleri safla\u015ft\u0131r\u0131rken ara\u015ft\u0131rmac\u0131lar ekstraksiyon solventi olarak monosikloheksen kullan\u0131r. D\u00fc\u015f\u00fck kaynama noktas\u0131, ekstrakte edilen bile\u015fiklerin kolayca ayr\u0131lmas\u0131n\u0131 sa\u011flar.<\/li>\n<li> Ara\u015ft\u0131rma ve Laboratuvar Uygulamalar\u0131: Monosikloheksen, stabilite, reaktivite ve \u00e7\u00f6z\u00fcc\u00fcl\u00fck \u00f6zelliklerinden dolay\u0131 \u00e7e\u015fitli deneyler ve reaksiyonlar i\u00e7in de\u011ferli bir laboratuvar reaktifi olarak hizmet eder.<\/li>\n<\/ul>\n<p> Monosikloheksenin uygulama \u00e7e\u015fitlili\u011fi kimya end\u00fcstrisinde, ara\u015ft\u0131rma laboratuvarlar\u0131nda ve \u00e7e\u015fitli \u00fcretim s\u00fcre\u00e7lerinde \u00f6nemini vurgulamaktad\u0131r.<\/p>\n<h2 class=\"wp-block-heading\"> <strong>Sorular:<\/strong><\/h2>\n<h3 class=\"wp-block-heading\"> S: Sikloheksen konsantre KMnO4 ile i\u015flendi\u011finde hangi bile\u015fik \u00fcretilir?<\/h3>\n<p> A: Monosikloheksen konsantre KMnO4 ile i\u015flendi\u011finde sikloheksanon bile\u015fi\u011fi \u00fcretilir.<\/p>\n<h3 class=\"wp-block-heading\"> S: IR kullanarak sikloheksan ile siklohekseni nas\u0131l ay\u0131rt edebilirsiniz?<\/h3>\n<p> A: Sikloheksan ve monosikloheksen, monosikloheksen spektrumunda 1630-1670 cm^-1 civar\u0131nda karakteristik bir C=C gerilme zirvesinin varl\u0131\u011f\u0131 veya yoklu\u011fu incelenerek IR spektroskopisi ile ay\u0131rt edilebilir.<\/p>\n<h3 class=\"wp-block-heading\"> S: Sikloheksen aromatik midir?<\/h3>\n<p> C: Hay\u0131r, monosikloheksen aromatik de\u011fildir. \u00c7ift ba\u011fa sahip siklik bir bile\u015fiktir ancak aromatik olarak de\u011ferlendirilmesi i\u00e7in gerekli kriterleri kar\u015f\u0131lamamaktad\u0131r.<\/p>\n<h3 class=\"wp-block-heading\"> S: Sikloheksen brominasyonu i\u00e7in ka\u00e7 olas\u0131 stereoizomer mevcuttur?<\/h3>\n<p> C: Monosikloheksenin brominasyonu i\u00e7in \u00e7ift ba\u011fa bromun eklenmesinden kaynaklanan iki olas\u0131 stereoizomer (cis ve trans) vard\u0131r.<\/p>\n<h3 class=\"wp-block-heading\"> Soru: Sikloheksenin a\u015fa\u011f\u0131dakilerden hangisiyle reaksiyonu sonucu doymam\u0131\u015f bir \u00fcr\u00fcn olu\u015fur?<\/h3>\n<p> A: Doymam\u0131\u015f bir \u00fcr\u00fcn, monosikloheksenin Diels-Alder reaksiyonunda bir dienofil ile reaksiyonundan kaynaklan\u0131r.<\/p>\n<h3 class=\"wp-block-heading\"> S: Sikloheksenin y\u00fczde verimi nas\u0131l bulunur?<\/h3>\n<p> C: Monosikloheksenin y\u00fczde verimi, monosikloheksenin ger\u00e7ek veriminin teorik verime b\u00f6l\u00fcnmesi ve ard\u0131ndan %100 ile \u00e7arp\u0131lmas\u0131yla hesaplanabilir.<\/p>\n<h3 class=\"wp-block-heading\"> S: Siklopentil metan-1-ol&#8217;u sikloheksen&#8217;e nas\u0131l d\u00f6n\u00fc\u015ft\u00fcrebilirim?<\/h3>\n<p> A: Siklopentil metan-1-ol, genellikle konsantre s\u00fclf\u00fcrik asit veya fosforik asit gibi bir asit kataliz\u00f6r\u00fc kullan\u0131larak dehidrasyona tabi tutularak monosikloheksen&#8217;e d\u00f6n\u00fc\u015ft\u00fcr\u00fclebilir.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Sikloheksen (C6H10), reaktivitesi ve \u00e7ok y\u00f6nl\u00fcl\u00fc\u011f\u00fc nedeniyle kimyasal reaksiyonlarda yayg\u0131n olarak bir \u00e7\u00f6z\u00fcc\u00fc ve ara madde olarak kullan\u0131lan siklik \u00e7ift ba\u011fl\u0131 bir hidrokarbondur. IUPAC Ad\u0131 sikloheksen Molek\u00fcler form\u00fcl C\u2086H\u2081\u2080 CAS numaras\u0131 110-83-8 E\u015f anlaml\u0131 Monosikloheksen, Heksanaften, 1,2-dihidrobenzen InChI InChI=1S\/C6H10\/c1-2-4-6-5-3-1\/h1-2H,3-6H2 Sikloheksenin \u00f6zellikleri Sikloheksen Form\u00fcl\u00fc Sikloheksenin form\u00fcl\u00fc, molek\u00fcler bile\u015fimini temsil eden C\u2086H\u2081\u2080&#8217;dir. Her bir karbon atomunun iki &#8230; <a title=\"Sikloheksen &#8211; c6h10, 110-83-8\" class=\"read-more\" href=\"https:\/\/chemuza.org\/tr\/sikloheksen-c6h10\/\" aria-label=\"More on Sikloheksen &#8211; c6h10, 110-83-8\">Devam\u0131n\u0131 oku<\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[5],"tags":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.4 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Sikloheksen - C6H10, 110-83-8<\/title>\n<meta name=\"description\" content=\"Sikloheksen (C6H10), kimyasal reaksiyonlarda genellikle bir \u00e7\u00f6z\u00fcc\u00fc ve ara madde olarak kullan\u0131lan, siklik \u00e7ift ba\u011fl\u0131 bir hidrokarbondur.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/chemuza.org\/tr\/sikloheksen-c6h10\/\" \/>\n<meta property=\"og:locale\" content=\"tr_TR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Sikloheksen - C6H10, 110-83-8\" \/>\n<meta property=\"og:description\" content=\"Sikloheksen (C6H10), kimyasal reaksiyonlarda genellikle bir \u00e7\u00f6z\u00fcc\u00fc ve ara madde olarak kullan\u0131lan, siklik \u00e7ift ba\u011fl\u0131 bir hidrokarbondur.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/chemuza.org\/tr\/sikloheksen-c6h10\/\" \/>\n<meta property=\"og:site_name\" content=\"Chemuza\" \/>\n<meta property=\"article:published_time\" content=\"2023-07-20T21:13:35+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/chemuza.org\/wp-content\/uploads\/2023\/08\/cyclohexene.jpg\" \/>\n<meta name=\"author\" content=\"Edit\u00f6r ekibi\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Yazan:\" \/>\n\t<meta name=\"twitter:data1\" content=\"Edit\u00f6r ekibi\" \/>\n\t<meta name=\"twitter:label2\" content=\"Tahmini okuma s\u00fcresi\" \/>\n\t<meta name=\"twitter:data2\" content=\"8 dakika\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\/\/chemuza.org\/tr\/sikloheksen-c6h10\/#article\",\"isPartOf\":{\"@id\":\"https:\/\/chemuza.org\/tr\/sikloheksen-c6h10\/\"},\"author\":{\"name\":\"Edit\u00f6r ekibi\",\"@id\":\"https:\/\/chemuza.org\/tr\/#\/schema\/person\/5d92b9b82b9b43578b70f5a7cd51fa3e\"},\"headline\":\"Sikloheksen &#8211; 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