{"id":498,"date":"2023-07-22T23:48:32","date_gmt":"2023-07-22T23:48:32","guid":{"rendered":"https:\/\/chemuza.org\/tr\/sikloheksanol\/"},"modified":"2023-07-22T23:48:32","modified_gmt":"2023-07-22T23:48:32","slug":"sikloheksanol","status":"publish","type":"post","link":"https:\/\/chemuza.org\/tr\/sikloheksanol\/","title":{"rendered":"Sikloheksanol \u2013 c6h11oh, 108-93-0"},"content":{"rendered":"<p>Sikloheksanol veya C6H11OH, hafif bir kokuya sahip, renksiz ya\u011fl\u0131 bir s\u0131v\u0131d\u0131r. Yayg\u0131n olarak solvent olarak ve naylon ve di\u011fer kimyasallar\u0131n \u00fcretiminde kullan\u0131l\u0131r.<\/p>\n<figure class=\"wp-block-table\">\n<table>\n<tbody>\n<tr>\n<td> IUPAC Ad\u0131<\/td>\n<td> Sikloheksanol<\/td>\n<\/tr>\n<tr>\n<td> Molek\u00fcler form\u00fcl<\/td>\n<td> C6H12O veya C6H11OH<\/td>\n<\/tr>\n<tr>\n<td> CAS numaras\u0131<\/td>\n<td> 108-93-0<\/td>\n<\/tr>\n<tr>\n<td> E\u015f anlaml\u0131<\/td>\n<td> Hekzahidrofenol; Hidrofenol; Sikloheksil alkol; Heksalin; Sikloheksanolol<\/td>\n<\/tr>\n<tr>\n<td> Kimyasal yap\u0131<\/td>\n<td> InChI=1S\/C6H12O\/c7-6-4-2-1-3-5-6\/h6-7H,1-5H2<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/figure>\n<h6 class=\"wp-block-heading\"> Sikloheksanol\u00fcn yap\u0131s\u0131 <\/h6>\n<div class=\"wp-block-image\">\n<figure class=\"alignright size-large\"><img decoding=\"async\" src=\"https:\/\/chemuza.org\/wp-content\/uploads\/2023\/08\/cyclohexanol.jpg\" alt=\"Sikloheksanol\" srcset=\"\" sizes=\"\"><\/figure>\n<\/div>\n<p> Sikloheksanol, karbon atomlar\u0131ndan birine ba\u011fl\u0131 bir hidroksil grubuna (-OH) sahip alt\u0131 \u00fcyeli bir karbon halkas\u0131na sahiptir. Sikloheksanol\u00fcn molek\u00fcler form\u00fcl\u00fc C6H12O&#8217;dur. Sikloheksan halkas\u0131, eksenel pozisyonda bulunan hidroksil grubu ile bir et yap\u0131s\u0131na sahiptir. Sikloheksanol\u00fcn yap\u0131s\u0131 \u00f6nemlidir \u00e7\u00fcnk\u00fc fiziksel ve kimyasal \u00f6zelliklerini belirler.<\/p>\n<h6 class=\"wp-block-heading\"> Sikloheksanol Form\u00fcl\u00fc<\/h6>\n<p> Sikloheksanol\u00fcn kimyasal form\u00fcl\u00fc C6H12O&#8217;dur. Bu, bir sikloheksanol molek\u00fcl\u00fcndeki atomlar\u0131n say\u0131s\u0131n\u0131 ve t\u00fcrlerini temsil eder. Form\u00fcl \u00f6nemlidir \u00e7\u00fcnk\u00fc bir reaksiyonda ihtiya\u00e7 duyulan sikloheksanol miktar\u0131n\u0131 hesaplamak i\u00e7in kullan\u0131l\u0131r. Ek olarak bir reaksiyonun stokiyometrisini belirlemek i\u00e7in kullan\u0131l\u0131r.<\/p>\n<h6 class=\"wp-block-heading\"> Sikloheksanol\u00fcn IR spektrumu<\/h6>\n<p> Sikloheksanol\u00fcn IR spektrumu, hidroksil grubunun (-OH) varl\u0131\u011f\u0131na ba\u011fl\u0131 olarak yakla\u015f\u0131k 3400 cm-1&#8217;de geni\u015f ve g\u00fc\u00e7l\u00fc bir zirve g\u00f6sterir. Bu zirve alkol\u00fcn varl\u0131\u011f\u0131n\u0131n g\u00f6stergesidir. Ek olarak spektrum, sikloheksan halkas\u0131n\u0131n varl\u0131\u011f\u0131na ba\u011fl\u0131 olarak 1000-1300 cm-1 aral\u0131\u011f\u0131nda birka\u00e7 tepe noktas\u0131 g\u00f6sterir. Siklohekzanol\u00fcn IR spektrumu \u00f6nemlidir \u00e7\u00fcnk\u00fc maddeyi tan\u0131mlamak ve karakterize etmek i\u00e7in kullan\u0131labilir.<\/p>\n<h6 class=\"wp-block-heading\"> Sikloheksanol Molar K\u00fctle<\/h6>\n<p> Bir sikloheksanol molek\u00fcl\u00fcn\u00fcn t\u00fcm atomlar\u0131n\u0131n atomik k\u00fctlelerinin toplam\u0131, onun molar k\u00fctlesini (100,16 g\/mol) hesaplamam\u0131z\u0131 sa\u011flar. Molar k\u00fctle, bir reaksiyonda gereken sikloheksanol miktar\u0131n\u0131n belirlenmesinde ve stokiyometrik hesaplamalarda gram ve mol aras\u0131nda d\u00f6n\u00fc\u015f\u00fcm yap\u0131lmas\u0131nda \u00e7ok \u00f6nemli bir rol oynar.<\/p>\n<h6 class=\"wp-block-heading\"> Sikloheksanol Kaynama noktas\u0131<\/h6>\n<p> Sikloheksanol\u00fcn kaynama noktas\u0131 161,5\u00b0C&#8217;dir (322,7\u00b0F). Bu, sikloheksanol\u00fcn s\u0131v\u0131 faz\u0131n\u0131n gaz faz\u0131na d\u00f6n\u00fc\u015ft\u00fc\u011f\u00fc s\u0131cakl\u0131kt\u0131r. Kaynama noktas\u0131 \u00f6nemli bir fiziksel \u00f6zelliktir \u00e7\u00fcnk\u00fc sikloheksanol\u00fc bir kar\u0131\u015f\u0131mdaki di\u011fer maddelerden safla\u015ft\u0131rmak ve ay\u0131rmak i\u00e7in kullan\u0131l\u0131r. Siklohekzanol\u00fcn nispeten y\u00fcksek kaynama noktas\u0131, onu y\u00fcksek s\u0131cakl\u0131k gerektiren reaksiyonlarda bir \u00e7\u00f6z\u00fcc\u00fc olarak faydal\u0131 k\u0131lar.<\/p>\n<h6 class=\"wp-block-heading\"> C6H11OH Erime noktas\u0131<\/h6>\n<p> C6H11OH&#8217;nin erime noktas\u0131 25,93\u00b0C&#8217;dir (78,67\u00b0F). Bu, C6H11OH&#8217;nin kat\u0131 faz\u0131n\u0131n s\u0131v\u0131 faza d\u00f6n\u00fc\u015ft\u00fc\u011f\u00fc s\u0131cakl\u0131kt\u0131r. Erime noktas\u0131 \u00f6nemli bir fiziksel \u00f6zelliktir \u00e7\u00fcnk\u00fc C6H11OH&#8217;yi tan\u0131mlamak ve karakterize etmek i\u00e7in kullan\u0131l\u0131r. Ayr\u0131ca C6H11OH&#8217;nin safl\u0131\u011f\u0131n\u0131 belirlemek i\u00e7in de kullan\u0131l\u0131r.<\/p>\n<h6 class=\"wp-block-heading\"> C6H11OH Yo\u011funluk g\/mL<\/h6>\n<p> C6H11OH&#8217;nin yo\u011funlu\u011fu 25\u00b0C&#8217;de (77\u00b0F) 0,962 g\/mL&#8217;dir. Bu, maddenin birim hacmi ba\u015f\u0131na C6H11OH k\u00fctlesidir. Yo\u011funluk \u00f6nemli bir fiziksel \u00f6zelliktir \u00e7\u00fcnk\u00fc bir reaksiyon i\u00e7in gereken C6H11OH k\u00fctlesini belirlemek i\u00e7in kullan\u0131l\u0131r. Ek olarak bir \u00e7\u00f6zeltideki C6H11OH konsantrasyonunu hesaplamak i\u00e7in kullan\u0131l\u0131r.<\/p>\n<h6 class=\"wp-block-heading\"> C6H11OH Molek\u00fcl A\u011f\u0131rl\u0131\u011f\u0131<\/h6>\n<p> C6H11OH&#8217;nin molek\u00fcler a\u011f\u0131rl\u0131\u011f\u0131 100,16 g\/mol&#8217;d\u00fcr. Bir C6H11OH molek\u00fcl\u00fcndeki t\u00fcm atomlar\u0131n atom a\u011f\u0131rl\u0131klar\u0131n\u0131n toplam\u0131d\u0131r. Molek\u00fcl a\u011f\u0131rl\u0131\u011f\u0131 \u00f6nemli bir \u00f6zelliktir \u00e7\u00fcnk\u00fc bir reaksiyonda ihtiya\u00e7 duyulan C6H11OH miktar\u0131n\u0131 hesaplamak i\u00e7in kullan\u0131l\u0131r. Ayr\u0131ca stokiyometrik hesaplamalarda gram ve mol aras\u0131nda d\u00f6n\u00fc\u015f\u00fcm yapmak i\u00e7in kullan\u0131l\u0131r.<\/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 s\u0131v\u0131<\/td>\n<\/tr>\n<tr>\n<td> Spesifik yer \u00e7ekimi<\/td>\n<td> 0,962 gr\/ml<\/td>\n<\/tr>\n<tr>\n<td> Renk<\/td>\n<td> Renksiz<\/td>\n<\/tr>\n<tr>\n<td> Koku<\/td>\n<td> Hafif koku<\/td>\n<\/tr>\n<tr>\n<td> Molar k\u00fctle<\/td>\n<td> 100,16 gr\/mol<\/td>\n<\/tr>\n<tr>\n<td> Yo\u011funluk<\/td>\n<td> 0,962 gr\/ml<\/td>\n<\/tr>\n<tr>\n<td> F\u00fczyon noktas\u0131<\/td>\n<td> 25,93\u00b0C (78,67\u00b0F)<\/td>\n<\/tr>\n<tr>\n<td> Kaynama noktas\u0131<\/td>\n<td> 161,5\u00b0C (322,7\u00b0F)<\/td>\n<\/tr>\n<tr>\n<td> Fla\u015f noktas\u0131<\/td>\n<td> 70\u00b0C (158\u00b0F)<\/td>\n<\/tr>\n<tr>\n<td> sudaki \u00e7\u00f6z\u00fcn\u00fcrl\u00fck<\/td>\n<td> kar\u0131\u015fabilir<\/td>\n<\/tr>\n<tr>\n<td> \u00e7\u00f6z\u00fcn\u00fcrl\u00fck<\/td>\n<td> Bir\u00e7ok organik \u00e7\u00f6z\u00fcc\u00fcde \u00e7\u00f6z\u00fcn\u00fcr<\/td>\n<\/tr>\n<tr>\n<td> Buhar bas\u0131nc\u0131<\/td>\n<td> 0,14 kPa (25\u00b0C&#8217;de)<\/td>\n<\/tr>\n<tr>\n<td> Buhar yo\u011funlu\u011fu<\/td>\n<td> 3,5 (hava = 1)<\/td>\n<\/tr>\n<tr>\n<td> pKa<\/td>\n<td> 16.1<\/td>\n<\/tr>\n<tr>\n<td> pH<\/td>\n<td> 6 ila 8<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/figure>\n<p> Not: Bu tabloda sunulan de\u011ferler yakla\u015f\u0131k de\u011ferlerdir ve bilgi kayna\u011f\u0131na g\u00f6re de\u011fi\u015fiklik g\u00f6sterebilir.<\/p>\n<h5 class=\"wp-block-heading\"> <strong>Sikloheksanol\u00fcn g\u00fcvenli\u011fi ve tehlikeleri<\/strong><\/h5>\n<p> C6H11OH belirli g\u00fcvenlik riskleri ve tehlikeleri olu\u015fturdu\u011fundan dikkatli kullan\u0131lmal\u0131d\u0131r. Bu kimyasala maruz kalmak ciltte, g\u00f6zlerde ve solunum sisteminde tahri\u015fe neden olabilir. Ayr\u0131ca solunmas\u0131 halinde ba\u015f a\u011fr\u0131s\u0131na, ba\u015f d\u00f6nmesine ve mide bulant\u0131s\u0131na neden olabilir. C6H11OH&#8217;nin yutulmas\u0131 kar\u0131n a\u011fr\u0131s\u0131, kusma ve ishale neden olabilir. Bu kimyasal yan\u0131c\u0131d\u0131r ve \u0131s\u0131ya veya aleve maruz kald\u0131\u011f\u0131nda tutu\u015fabilir. Serin ve kuru bir yerde, \u0131s\u0131dan ve tutu\u015fturucu kaynaklardan uzakta saklanmas\u0131 ve kullan\u0131lmas\u0131 \u00f6nemlidir. C6H11OH ile \u00e7al\u0131\u015f\u0131rken eldiven, g\u00f6zl\u00fck ve solunum cihaz\u0131 gibi koruyucu ekipmanlar kullan\u0131lmal\u0131d\u0131r. Maruz kalma durumunda derhal t\u0131bbi yard\u0131ma ba\u015fvurun.<\/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> S26 \u2013 G\u00f6zle temas\u0131 halinde derhal bol su ile y\u0131kay\u0131n ve doktora ba\u015fvurun.&lt;br&gt; S36\/37\/39 \u2013 Uygun koruyucu k\u0131yafet, eldiven ve g\u00f6z\/g\u00f6z koruyucu ekipman kullan\u0131n. Y\u00fcz.&lt;br&gt;S45 \u2013 Kaza durumunda veya kendinizi iyi hissetmiyorsan\u0131z derhal bir doktora ba\u015fvurun (m\u00fcmk\u00fcnse doktora etiketi g\u00f6sterin).<\/td>\n<\/tr>\n<tr>\n<td> B\u0130R tan\u0131mlay\u0131c\u0131lar<\/td>\n<td> UN1986<\/td>\n<\/tr>\n<tr>\n<td> HS kodu<\/td>\n<td> 2907.13.00<\/td>\n<\/tr>\n<tr>\n<td> Tehlike s\u0131n\u0131f\u0131<\/td>\n<td> 3<\/td>\n<\/tr>\n<tr>\n<td> Paketleme grubu<\/td>\n<td> III<\/td>\n<\/tr>\n<tr>\n<td> Toksisite<\/td>\n<td> D\u00fc\u015f\u00fck ila orta derecede toksisite<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/figure>\n<h5 class=\"wp-block-heading\"> <strong>Sikloheksanol sentez y\u00f6ntemleri<\/strong><\/h5>\n<p> C6H11OH \u00e7e\u015fitli y\u00f6ntemlerle sentezlenebilir.<\/p>\n<ol>\n<li> C6H11OH \u00fcretmenin yayg\u0131n bir y\u00f6ntemi, fenol\u00fcn nikel veya platin gibi bir metal kataliz\u00f6r varl\u0131\u011f\u0131nda katalitik olarak hidrojenlenmesidir. Bu y\u00f6ntem, fenol\u00fcn aromatik halkas\u0131n\u0131n C6H11OH olu\u015fturacak \u015fekilde indirgenmesini i\u00e7erir.<\/li>\n<li> Ba\u015fka bir y\u00f6ntem, bak\u0131r veya kobalt gibi bir kataliz\u00f6r varl\u0131\u011f\u0131nda hava veya oksijen kullan\u0131larak sikloheksan\u0131n oksidasyonunu i\u00e7erir. Bu i\u015flem, sikloheksanon olu\u015fturmak \u00fczere daha da oksitlenebilen bir ara \u00fcr\u00fcn olarak C6H11OH \u00fcretir.<\/li>\n<li> C6H11OH ayr\u0131ca sikloheksil asetat\u0131n asidik veya bazik bir kataliz\u00f6r kullan\u0131larak hidrolizi yoluyla da elde edilebilir. Bu y\u00f6ntem, C6H11OH ve asetik asit olu\u015fturmak \u00fczere sikloheksil asetattaki ester ba\u011f\u0131n\u0131n b\u00f6l\u00fcnmesini i\u00e7erir.<\/li>\n<li> Sikloheksanon oksimin kataliz\u00f6r olarak s\u00fclf\u00fcrik asit kullan\u0131larak Beckmann yeniden d\u00fczenlenmesi, C6H11OH&#8217;yi sentezlemek i\u00e7in ba\u015fka bir y\u00f6ntemdir. Bu i\u015flem, C6H11OH \u00fcretmek \u00fczere hidrolize edilebilen bir amid ara maddesi olu\u015fturmak \u00fczere sikloheksanon oksimdeki oksim grubunun yeniden d\u00fczenlenmesini i\u00e7erir.<\/li>\n<\/ol>\n<p> Genel olarak, C6H11OH&#8217;nin sentezi bireylerin \u00e7e\u015fitli kimyasal i\u015flemleri ger\u00e7ekle\u015ftirmesini ve uygun g\u00fcvenlik \u00f6nlemlerini ve ekipmanlar\u0131n\u0131 kullanmas\u0131n\u0131 gerektirir.<\/p>\n<h5 class=\"wp-block-heading\"> <strong>Sikloheksanol\u00fcn kullan\u0131m alanlar\u0131<\/strong><\/h5>\n<p> C6H11OH&#8217;un farkl\u0131 end\u00fcstrilerde bir\u00e7ok uygulamas\u0131 vard\u0131r.<\/p>\n<ul>\n<li> End\u00fcstriler, cilalar, vernikler ve re\u00e7ineler \u00fcretmek i\u00e7in bir \u00e7\u00f6z\u00fcc\u00fc olarak ve ila\u00e7 end\u00fcstrisinde ila\u00e7 haz\u0131rlamak i\u00e7in bir \u00e7\u00f6z\u00fcc\u00fc olarak C6H11OH&#8217;yi kullan\u0131r.<\/li>\n<li> C6H11OH, naylon \u00fcretiminde gerekli bir bile\u015fen olan adipik asit \u00fcretiminde \u00f6nemli bir ara madde olarak hizmet eder. Ayn\u0131 zamanda bisfenol A, sikloheksanon ve kaprolaktam dahil olmak \u00fczere \u00e7e\u015fitli kimyasallar\u0131n sentezi i\u00e7in hammadde g\u00f6revi g\u00f6r\u00fcr.<\/li>\n<li> Petrol end\u00fcstrisi, boru hatlar\u0131nda ve depolama tanklar\u0131nda korozyonu \u00f6nlemek i\u00e7in ham petrole korozyon \u00f6nleyici olarak C6H11OH ekler.<\/li>\n<li> \u00dcreticiler, plastiklerin esnekli\u011fini ve dayan\u0131kl\u0131l\u0131\u011f\u0131n\u0131 art\u0131ran plastikle\u015ftiriciler \u00fcretmek i\u00e7in C6H11OH kullan\u0131yor. Ayn\u0131 zamanda parf\u00fcm ve kozmetik \u00fcr\u00fcnlerinde de yayg\u0131n olarak kullan\u0131lan bir maddedir.<\/li>\n<li> C6H11OH, \u0131s\u0131 transfer s\u0131v\u0131s\u0131, ya\u011flay\u0131c\u0131 ve b\u00f6cek ilac\u0131 olarak kullan\u0131l\u0131r. Ayr\u0131ca organik sentezlerde ve laboratuvar deneylerinde reaktif olarak g\u00f6rev yapar.<\/li>\n<\/ul>\n<p> Genel olarak C6H11OH, \u00e7e\u015fitli end\u00fcstrilerde geni\u015f bir uygulama alan\u0131na sahiptir ve \u00e7ok y\u00f6nl\u00fc \u00f6zellikleri, onu bir\u00e7ok end\u00fcstriyel s\u00fcre\u00e7te \u00f6nemli bir kimyasal haline getirir.<\/p>\n<h5 class=\"wp-block-heading\"> <strong>Sorular:<\/strong><\/h5>\n<h6 class=\"wp-block-heading\"> Sikloheksanol suda \u00e7\u00f6z\u00fcn\u00fcr m\u00fc?<\/h6>\n<p> Sikloheksanol suda orta derecede \u00e7\u00f6z\u00fcn\u00fcr, ancak \u00e7\u00f6z\u00fcn\u00fcrl\u00fc\u011f\u00fc s\u0131cakl\u0131k artt\u0131k\u00e7a azal\u0131r. Etanol, dietil eter ve aseton gibi organik \u00e7\u00f6z\u00fcc\u00fclerde daha fazla \u00e7\u00f6z\u00fcn\u00fcr. C6H11OH&#8217;nin sudaki \u00e7\u00f6z\u00fcn\u00fcrl\u00fc\u011f\u00fc, C6H11OH&#8217;nin hidroksil grubu ile su molek\u00fclleri aras\u0131nda hidrojen ba\u011flar\u0131n\u0131n olu\u015fmas\u0131ndan kaynaklanmaktad\u0131r. Bununla birlikte, C6H11OH&#8217;nin hidrofobik sikloheksan halkas\u0131 genel polaritesini azaltarak onu metanol ve etanol gibi di\u011fer daha polar alkollere g\u00f6re suda daha az \u00e7\u00f6z\u00fcn\u00fcr hale getirir. C6H11OH&#8217;nin sudaki \u00e7\u00f6z\u00fcn\u00fcrl\u00fc\u011f\u00fc, \u00e7\u00f6z\u00fcc\u00fc olarak kullan\u0131m\u0131nda ve ortam olarak suyun kullan\u0131ld\u0131\u011f\u0131 end\u00fcstriyel i\u015flemlerde \u00f6nemli bir husustur.<\/p>\n<h6 class=\"wp-block-heading\"> A\u015fa\u011f\u0131daki reaksiyon serilerinden hangisi sikloheksanol\u00fc 1,2-epoksisikloheksana d\u00f6n\u00fc\u015ft\u00fcr\u00fcr?<\/h6>\n<p> Sikloheksanol\u00fc 1,2-epoksisikloheksana d\u00f6n\u00fc\u015ft\u00fcrmek i\u00e7in a\u015fa\u011f\u0131daki reaksiyonlar ger\u00e7ekle\u015ftirilebilir:<\/p>\n<ol type=\"1\" start=\"1\">\n<li> Sikloheksanol ilk \u00f6nce dehidrasyon yoluyla sikloheksen olu\u015fturmak i\u00e7in s\u00fclf\u00fcrik asit gibi g\u00fc\u00e7l\u00fc bir asit kataliz\u00f6r\u00fcyle i\u015flenir.<\/li>\n<li> Elde edilen sikloheksen daha sonra m-kloroperbenzoik asit (MCPBA) gibi bir perasit ile reaksiyona girerek bir epoksit, \u00f6zellikle 1,2-epoksisikloheksan olu\u015fturur.<\/li>\n<\/ol>\n<p> Bu nedenle, siklohekzanol\u00fcn 1,2-epoksisikloheksana d\u00f6n\u00fc\u015ft\u00fcr\u00fclmesine y\u00f6nelik do\u011fru reaksiyon serisi, sikloheksanol\u00fcn sikloheksen olu\u015fturmak \u00fczere dehidrasyonunu ve ard\u0131ndan bir perasit kullan\u0131larak 1,2-epoksisikloheksan olu\u015fturmak \u00fczere sikloheksenin epoksidasyonunu i\u00e7erir.<\/p>\n<h6 class=\"wp-block-heading\"> Siklohekzanol\u00fcn neden bir say\u0131 \u00f6nekine ihtiyac\u0131 yok?<\/h6>\n<p> Sikloheksanol, sikloheksanol\u00fcn tek bir izomeri oldu\u011fundan ad\u0131nda bir say\u0131 \u00f6nekine ihtiya\u00e7 duymaz. \u0130zomerler ayn\u0131 molek\u00fcler form\u00fcle sahip ancak atomlar\u0131n farkl\u0131 yap\u0131sal d\u00fczenlemelerine sahip molek\u00fcllerdir. Sikloheksanol, bir sikloheksan halkas\u0131na ba\u011fl\u0131 tek bir hidroksil fonksiyonel grubuna (-OH) sahiptir ve molek\u00fcler form\u00fcl\u00fc C6H12O&#8217;dur. Siklohekzanolde atomlar\u0131n tek bir olas\u0131 d\u00fczeni oldu\u011fundan konumunu veya fonksiyonel gruplar\u0131n say\u0131s\u0131n\u0131 belirtmek i\u00e7in say\u0131sal bir \u00f6nek gerektirmez. Buna kar\u015f\u0131l\u0131k, sikloheksanon ve sikloheksanedion gibi di\u011fer bile\u015fikler, farkl\u0131 konumlara ve say\u0131da karbonil grubuna sahip birden fazla izomer i\u00e7erir ve bu nedenle, fonksiyonel gruplar\u0131n konumunu belirtmek i\u00e7in say\u0131 \u00f6nekleri gerektirir.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Sikloheksanol veya C6H11OH, hafif bir kokuya sahip, renksiz ya\u011fl\u0131 bir s\u0131v\u0131d\u0131r. Yayg\u0131n olarak solvent olarak ve naylon ve di\u011fer kimyasallar\u0131n \u00fcretiminde kullan\u0131l\u0131r. IUPAC Ad\u0131 Sikloheksanol Molek\u00fcler form\u00fcl C6H12O veya C6H11OH CAS numaras\u0131 108-93-0 E\u015f anlaml\u0131 Hekzahidrofenol; Hidrofenol; Sikloheksil alkol; Heksalin; Sikloheksanolol Kimyasal yap\u0131 InChI=1S\/C6H12O\/c7-6-4-2-1-3-5-6\/h6-7H,1-5H2 Sikloheksanol\u00fcn yap\u0131s\u0131 Sikloheksanol, karbon atomlar\u0131ndan birine ba\u011fl\u0131 bir hidroksil grubuna (-OH) &#8230; <a title=\"Sikloheksanol \u2013 c6h11oh, 108-93-0\" class=\"read-more\" href=\"https:\/\/chemuza.org\/tr\/sikloheksanol\/\" aria-label=\"More on Sikloheksanol \u2013 c6h11oh, 108-93-0\">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>Sikloheksanol - C6H11OH, 108-93-0<\/title>\n<meta name=\"description\" content=\"Sikloheksanol veya C6H11OH, hafif bir kokuya sahip, renksiz ya\u011fl\u0131 bir s\u0131v\u0131d\u0131r. 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