{"id":538,"date":"2023-07-22T18:23:57","date_gmt":"2023-07-22T18:23:57","guid":{"rendered":"https:\/\/chemuza.org\/tr\/siklopentanon-c5h8o\/"},"modified":"2023-07-22T18:23:57","modified_gmt":"2023-07-22T18:23:57","slug":"siklopentanon-c5h8o","status":"publish","type":"post","link":"https:\/\/chemuza.org\/tr\/siklopentanon-c5h8o\/","title":{"rendered":"Siklopentanon &#8211; c5h8o, 120-92-3"},"content":{"rendered":"<p>Siklopentanon, C5H8O molek\u00fcler form\u00fcl\u00fcne sahip siklik bir organik bile\u015fiktir. \u00c7e\u015fitli kimyasallar\u0131n sentezinde yayg\u0131n olarak \u00e7\u00f6z\u00fcc\u00fc ve \u00f6nc\u00fc olarak kullan\u0131l\u0131r.<\/p>\n<figure class=\"wp-block-table\">\n<table>\n<tbody>\n<tr>\n<td> IUPAC Ad\u0131<\/td>\n<td> Siklopentanon<\/td>\n<\/tr>\n<tr>\n<td> Molek\u00fcler form\u00fcl<\/td>\n<td> C5H8O<\/td>\n<\/tr>\n<tr>\n<td> CAS numaras\u0131<\/td>\n<td> 120-92-3<\/td>\n<\/tr>\n<tr>\n<td> E\u015f anlaml\u0131<\/td>\n<td> Ketosiklopentan, CPK, adipik keton, siklopentanon, ketopentametilen, 1-oksosiklopentan<\/td>\n<\/tr>\n<tr>\n<td> InChI<\/td>\n<td> InChI=1S\/C5H8O\/c6-5-3-1-2-4-5\/h1-4H2<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/figure>\n<h6 class=\"wp-block-heading\"> Siklopentanonun molar k\u00fctlesi<\/h6>\n<p> Siklopentanonun molar k\u00fctlesi yakla\u015f\u0131k 84,13 g\/mol&#8217;d\u00fcr. Bu de\u011fer, bile\u015fi\u011fin tek bir molek\u00fcl\u00fcndeki t\u00fcm atomlar\u0131n atom a\u011f\u0131rl\u0131klar\u0131 toplanarak hesaplanabilir. Bu durumda, her biri atom a\u011f\u0131rl\u0131\u011f\u0131 12,01 g\/mol olan be\u015f karbon atomu, her biri atom a\u011f\u0131rl\u0131\u011f\u0131 1,01 g\/mol olan sekiz hidrojen atomu ve atom a\u011f\u0131rl\u0131\u011f\u0131 16,00 g\/mol olan bir oksijen atomu vard\u0131r. Bu nedenle siklopentanonun toplam molar k\u00fctlesi 5 x 12,01 + 8 x 1,01 + 16,00 = 84,13 g\/mol&#8217;d\u00fcr.<\/p>\n<h6 class=\"wp-block-heading\"> Siklopentanonun kaynama noktas\u0131<\/h6>\n<p> Siklopentanon, standart atmosferik bas\u0131n\u00e7ta (1 atm) yakla\u015f\u0131k 130-132\u00b0C kaynama noktas\u0131na sahiptir. Bir bile\u015fi\u011fin kaynama noktas\u0131, standart atmosfer bas\u0131nc\u0131nda s\u0131v\u0131 halden gaz haline ge\u00e7ti\u011fi s\u0131cakl\u0131kt\u0131r. Siklopentanon, k\u00fc\u00e7\u00fck boyutu ve nispeten zay\u0131f molek\u00fcller aras\u0131 kuvvetleri nedeniyle nispeten d\u00fc\u015f\u00fck bir kaynama noktas\u0131na sahiptir. Oda s\u0131cakl\u0131\u011f\u0131nda kolayca buharla\u015fabilen u\u00e7ucu bir bile\u015fiktir.<\/p>\n<h6 class=\"wp-block-heading\"> Siklopentanonun erime noktas\u0131<\/h6>\n<p> Siklopentanonun erime noktas\u0131 yakla\u015f\u0131k -47\u00b0C&#8217;dir. Bir bile\u015fi\u011fin erime noktas\u0131, onun kat\u0131 halden s\u0131v\u0131 hale ge\u00e7ti\u011fi s\u0131cakl\u0131kt\u0131r. Siklopentanon, oda s\u0131cakl\u0131\u011f\u0131nda ve atmosferik bas\u0131n\u00e7ta renksiz bir s\u0131v\u0131 oldu\u011fundan erime noktas\u0131 genellikle \u00f6nemli de\u011fildir. Ancak d\u00fc\u015f\u00fck s\u0131cakl\u0131klarda kat\u0131la\u015fabilir ve erime noktas\u0131 safl\u0131\u011f\u0131n\u0131n belirlenmesinde faydal\u0131d\u0131r.<\/p>\n<h6 class=\"wp-block-heading\"> Siklopentanonun yo\u011funlu\u011fu g\/ml<\/h6>\n<p> Siklopentanonun oda s\u0131cakl\u0131\u011f\u0131nda ve standart atmosfer bas\u0131nc\u0131nda yo\u011funlu\u011fu yakla\u015f\u0131k 0,96 g\/mL&#8217;dir. Bir bile\u015fi\u011fin yo\u011funlu\u011fu, maddenin birim hacim ba\u015f\u0131na k\u00fctlesidir. Siklopentanon, suya (1 g\/mL) ve di\u011fer bir\u00e7ok organik \u00e7\u00f6z\u00fcc\u00fcye k\u0131yasla nispeten d\u00fc\u015f\u00fck bir yo\u011funlu\u011fa sahiptir. Bu d\u00fc\u015f\u00fck yo\u011funluk, onu daha az yo\u011fun bir solventin gerekli oldu\u011fu belirli uygulamalar i\u00e7in yararl\u0131 bir solvent haline getirir.<\/p>\n<h6 class=\"wp-block-heading\"> Siklopentanonun Molek\u00fcler A\u011f\u0131rl\u0131\u011f\u0131<\/h6>\n<p> Siklopentanonun molek\u00fcler a\u011f\u0131rl\u0131\u011f\u0131 84,13 g\/mol&#8217;d\u00fcr. Molek\u00fcl a\u011f\u0131rl\u0131\u011f\u0131, bir molek\u00fcldeki t\u00fcm atomlar\u0131n atom a\u011f\u0131rl\u0131klar\u0131n\u0131n toplam\u0131d\u0131r. Siklopentanon durumunda molek\u00fcl 5 karbon atomu, 8 hidrojen atomu ve 1 oksijen atomu i\u00e7erir. Molek\u00fcl a\u011f\u0131rl\u0131\u011f\u0131 genellikle kimyasal hesaplamalarda bir reaksiyonda bir maddenin ne kadar\u0131na ihtiya\u00e7 duyuldu\u011funu veya ne kadar\u0131n\u0131n \u00fcretildi\u011fini belirlemek i\u00e7in kullan\u0131l\u0131r. <\/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\/cyclopentanone.jpg\" alt=\"Siklopentanon\" width=\"182\" height=\"106\" srcset=\"\" sizes=\"\"><\/figure>\n<\/div>\n<h6 class=\"wp-block-heading\"> Siklopentanonun yap\u0131s\u0131<\/h6>\n<p> Siklopentanon, be\u015f \u00fcyeli karbon atomu halkas\u0131 ve bir oksijen atomundan olu\u015fan siklik bir yap\u0131ya sahiptir. Oksijen atomu, bile\u015fi\u011fe karakteristik reaktivitesini veren karbonil grubunun (C=O) bir par\u00e7as\u0131d\u0131r. Siklopentanonun siklik yap\u0131s\u0131 onu di\u011fer bir\u00e7ok organik bile\u015fi\u011fin sentezi i\u00e7in yararl\u0131 bir ba\u015flang\u0131\u00e7 malzemesi haline getirir.<\/p>\n<h6 class=\"wp-block-heading\"> Siklopentanon form\u00fcl\u00fc<\/h6>\n<p> Siklopentanonun molek\u00fcler form\u00fcl\u00fc C5H8O&#8217;dur. Bu form\u00fcl, bile\u015fi\u011fin bir molek\u00fcl\u00fcndeki her bir elementin atom say\u0131s\u0131n\u0131 g\u00f6sterir. Bu durumda form\u00fcl, her siklopentanon molek\u00fcl\u00fcnde 5 karbon atomu, 8 hidrojen atomu ve 1 oksijen atomu bulundu\u011funu g\u00f6sterir. Form\u00fcl, bile\u015fi\u011fin molek\u00fcler a\u011f\u0131rl\u0131\u011f\u0131n\u0131 hesaplamak ve kimyasal \u00f6zelliklerini anlamak i\u00e7in kullan\u0131\u015fl\u0131d\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> 20\u00b0C&#8217;de 0,960 g\/mL<\/td>\n<\/tr>\n<tr>\n<td> Renk<\/td>\n<td> Renksiz<\/td>\n<\/tr>\n<tr>\n<td> Koku<\/td>\n<td> Kafur kokusu<\/td>\n<\/tr>\n<tr>\n<td> Molar k\u00fctle<\/td>\n<td> 84,13 gr\/mol<\/td>\n<\/tr>\n<tr>\n<td> Yo\u011funluk<\/td>\n<td> 20\u00b0C&#8217;de 0,960 g\/mL<\/td>\n<\/tr>\n<tr>\n<td> F\u00fczyon noktas\u0131<\/td>\n<td> -47\u00b0C<\/td>\n<\/tr>\n<tr>\n<td> Kaynama noktas\u0131<\/td>\n<td> 130-132\u00b0C<\/td>\n<\/tr>\n<tr>\n<td> Fla\u015f noktas\u0131<\/td>\n<td> 38\u00b0C (kapal\u0131 kap)<\/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> \u00c7o\u011fu organik \u00e7\u00f6z\u00fcc\u00fcyle kar\u0131\u015fabilir<\/td>\n<\/tr>\n<tr>\n<td> Buhar bas\u0131nc\u0131<\/td>\n<td> 25\u00b0C&#8217;de 3,3 mmHg<\/td>\n<\/tr>\n<tr>\n<td> Buhar yo\u011funlu\u011fu<\/td>\n<td> 3,0 (hava = 1)<\/td>\n<\/tr>\n<tr>\n<td> pKa<\/td>\n<td> 16.7<\/td>\n<\/tr>\n<tr>\n<td> pH<\/td>\n<td> Uygulanamaz<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/figure>\n<h6 class=\"wp-block-heading\"> <strong>Siklopentanonun g\u00fcvenli\u011fi ve tehlikeleri<\/strong><\/h6>\n<p> Siklopentanon, uygun \u015fekilde kullan\u0131lmazsa \u00e7e\u015fitli g\u00fcvenlik riskleri olu\u015fturabilir. Yan\u0131c\u0131 bir s\u0131v\u0131d\u0131r ve bir \u0131s\u0131 kayna\u011f\u0131na veya aleve maruz kald\u0131\u011f\u0131nda tutu\u015fabilir. Ayr\u0131ca cilt veya g\u00f6zlerle temas\u0131 halinde tahri\u015fe ve yan\u0131klara neden olabilir. Buhar\u0131n\u0131 solumak ba\u015f a\u011fr\u0131s\u0131na, ba\u015f d\u00f6nmesine ve mide bulant\u0131s\u0131na neden olabilir. Siklopentanonla \u00e7al\u0131\u015f\u0131rken eldiven, g\u00f6zl\u00fck ve laboratuvar \u00f6nl\u00fc\u011f\u00fc gibi uygun koruyucu ekipmanlar\u0131n kullan\u0131lmas\u0131 \u00f6nemlidir. Serin ve kuru bir yerde, \u0131s\u0131 kaynaklar\u0131ndan ve uyumsuz maddelerden uzakta saklanmal\u0131d\u0131r. D\u00f6k\u00fcnt\u00fcler derhal temizlenmeli ve alan iyi havaland\u0131r\u0131lmal\u0131d\u0131r.<\/p>\n<figure class=\"wp-block-table\">\n<table>\n<tbody>\n<tr>\n<td> Tehlike sembolleri<\/td>\n<td> F, Xi<\/td>\n<\/tr>\n<tr>\n<td> G\u00fcvenlik A\u00e7\u0131klamas\u0131<\/td>\n<td> Tutu\u015fturucu kaynaklardan uzak tutun &#8211; Sigara i\u00e7meyin. Cilt ve g\u00f6zlerle temas\u0131ndan ka\u00e7\u0131n\u0131n. Uygun koruyucu k\u0131yafet, eldiven ve g\u00f6z\/y\u00fcz korumas\u0131 kullan\u0131n. Kaza durumunda veya kendinizi iyi hissetmiyorsan\u0131z derhal t\u0131bbi yard\u0131m isteyin (m\u00fcmk\u00fcnse etiketi g\u00f6sterin).<\/td>\n<\/tr>\n<tr>\n<td> BM kimlik numaralar\u0131<\/td>\n<td> BM 2245<\/td>\n<\/tr>\n<tr>\n<td> HS kodu<\/td>\n<td> 291429<\/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> Siklopentanon d\u00fc\u015f\u00fck toksisiteli bir madde olarak kabul edilir. Ancak ciltte, g\u00f6zlerde ve solunum sisteminde tahri\u015fe neden olabilir. Uzun s\u00fcreli maruz kalma karaci\u011fer ve b\u00f6brek hasar\u0131na neden olabilir. Siklopentanonun dikkatli bir \u015fekilde kullan\u0131lmas\u0131 ve uygun g\u00fcvenlik protokollerinin takip edilmesi \u00f6nemlidir.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/figure>\n<h6 class=\"wp-block-heading\"> <strong>Siklopentanonun sentezi i\u00e7in y\u00f6ntemler<\/strong><\/h6>\n<p> Siklopentanon \u00e7e\u015fitli y\u00f6ntemlerle sentezlenebilir. Yayg\u0131n bir y\u00f6ntem, fenol\u00fcn paladyum gibi bir metal kataliz\u00f6r \u00fczerinde hidrojen gaz\u0131 ile reaksiyonunu i\u00e7eren fenol hidrojenasyonudur. Ba\u015fka bir y\u00f6ntem, potasyum permanganat veya ozon gaz\u0131 kullan\u0131larak siklopentenin oksidasyonunu i\u00e7erir. Bu reaksiyon siklopentanonun yan\u0131 s\u0131ra karboksilik asitler gibi di\u011fer yan \u00fcr\u00fcnleri de \u00fcretir.<\/p>\n<p> Siklopentanonu sentezlemek i\u00e7in, siklopentanon vermek \u00fczere daha da hidrolize edilebilen siklik bir ara madde olu\u015fturmak \u00fczere siklopentadien ile maleik anhidrit aras\u0131nda bir Diels-Alder reaksiyonu ger\u00e7ekle\u015ftirilebilir. Ba\u015fka bir yakla\u015f\u0131m, adipik asidin, fosfor pentoksit gibi bir dehidrasyon maddesinin varl\u0131\u011f\u0131nda bir dekarboksilasyon reaksiyonuna tabi tutulmas\u0131ndan olu\u015fur. Bu y\u00f6ntem ayn\u0131 zamanda siklopentanon da \u00fcretir.<\/p>\n<p> Siklopentanonun sentezlenmesine y\u00f6nelik di\u011fer y\u00f6ntemler aras\u0131nda, siklopentilmagnezyum brom\u00fcr\u00fcn karbon dioksit ile reaksiyonunu ve kobalt karbonil gibi bir metal kataliz\u00f6r\u00fcn varl\u0131\u011f\u0131nda siklopentenin karbon monoksit ile reaksiyonunu i\u00e7erir.<\/p>\n<p> Siklopentanon sentez y\u00f6nteminin se\u00e7imi, ham maddelerin mevcudiyeti, \u00fcr\u00fcn\u00fcn istenen safl\u0131\u011f\u0131 ve istenen reaksiyon ko\u015fullar\u0131 gibi \u00e7e\u015fitli fakt\u00f6rlere ba\u011fl\u0131 olacakt\u0131r. Bu kimyasallarla \u00e7al\u0131\u015f\u0131rken uygun g\u00fcvenlik protokollerinin ve ekipmanlar\u0131n\u0131n kullan\u0131lmas\u0131 \u00f6nemlidir.<\/p>\n<h6 class=\"wp-block-heading\"> <strong>Siklopentanonun kullan\u0131m alanlar\u0131<\/strong><\/h6>\n<p> Siklopentanonun \u00e7e\u015fitli uygulamalarda kullan\u0131lmas\u0131 onu \u00e7ok y\u00f6nl\u00fc bir kimyasal haline getirir.<\/p>\n<ul>\n<li> Parf\u00fcm, b\u00f6cek ilac\u0131 ve ila\u00e7 gibi kimyasallar\u0131n \u00fcretiminde solvent olarak kullan\u0131l\u0131r.<\/li>\n<li> Adipik asit, siklopentilamin ve siklopentanol dahil olmak \u00fczere di\u011fer kimyasallar\u0131n sentezinde \u00f6nc\u00fc g\u00f6revi g\u00f6r\u00fcr.<\/li>\n<li> \u0130la\u00e7 end\u00fcstrisi, antiinflamatuar maddeler, antihistaminikler ve kas gev\u015feticiler gibi ila\u00e7lar\u0131n \u00fcretiminde siklopentanonu bir ara madde olarak kullan\u0131r.<\/li>\n<li> G\u0131da end\u00fcstrisi kafur kokusundan dolay\u0131 aroma maddesi olarak kullan\u0131r.<\/li>\n<li> Siklopentanon ayr\u0131ca polyester, naylon ve poli\u00fcretan gibi polimerlerin \u00fcretiminde de kullan\u0131l\u0131r; burada dayan\u0131kl\u0131l\u0131k, esneklik ve \u0131s\u0131ya ve kimyasallara kar\u015f\u0131 diren\u00e7 gibi \u00f6zellikler kazand\u0131r\u0131r.<\/li>\n<li> Karbon-karbon ba\u011flar\u0131n\u0131n olu\u015fumu ve siklik bile\u015fiklerin haz\u0131rlanmas\u0131 gibi organik kimya reaksiyonlar\u0131nda reaktif olarak siklopentanon kullan\u0131l\u0131r.<\/li>\n<li> B\u00f6cek \u00f6ld\u00fcr\u00fcc\u00fcler ve herbisitler gibi tar\u0131msal kimyasallar, imalatlar\u0131nda siklopentanon kullan\u0131r.<\/li>\n<\/ul>\n<p> Sonu\u00e7 olarak, siklopentanonun \u00e7ok y\u00f6nl\u00fcl\u00fc\u011f\u00fc onu farmas\u00f6tikten tar\u0131ma ve polimerlere kadar \u00e7e\u015fitli end\u00fcstrilerde \u00f6nemli bir kimyasal haline getirmektedir.<\/p>\n<p> <strong>Sorular:<\/strong><\/p>\n<h6 class=\"wp-block-heading\"> S: Siklopentanonun IR spektrumu neye benziyor?<\/h6>\n<p> A: Siklopentanonun IR spektrumu genellikle yakla\u015f\u0131k 1715-1740 cm^-1&#8217;de g\u00fc\u00e7l\u00fc bir karbonil (C=O) absorpsiyon band\u0131n\u0131n yan\u0131 s\u0131ra 2,850 ila 3,000 cm^-1 aral\u0131\u011f\u0131nda CH germe ve b\u00fckme bantlar\u0131 g\u00f6sterir.<\/p>\n<h6 class=\"wp-block-heading\"> S: Sikloheksilamin, siklopentanon ile reaksiyona girerek bir enamin olu\u015fturur mu?<\/h6>\n<p> C: Evet, sikloheksilamin siklopentanon ile reaksiyona girerek bir enamin olu\u015fturabilir. Reaksiyon, amin nitrojenin bir asit kataliz\u00f6r\u00fc ile protonasyonunu, ard\u0131ndan serbest nitrojen \u00e7iftinin siklopentanonun karbonil grubuna n\u00fckleofilik eklenmesini i\u00e7erir. Ortaya \u00e7\u0131kan \u00fcr\u00fcn, nitrojen ile siklopentanonun alfa karbonu aras\u0131nda bir karbon-karbon \u00e7ift ba\u011f\u0131 i\u00e7eren bir enamindir.<\/p>\n<h6 class=\"wp-block-heading\"> S: Siklopentanon end\u00fcstriyel olarak nas\u0131l \u00fcretilir?<\/h6>\n<p> C: Siklopentanon, paladyum gibi bir metal kataliz\u00f6r kullan\u0131larak fenol\u00fcn hidrojenlenmesi ve potasyum permanganat veya ozon gaz\u0131 kullan\u0131larak siklopentenin oksidasyonu dahil olmak \u00fczere \u00e7e\u015fitli y\u00f6ntemlerle end\u00fcstriyel olarak \u00fcretilebilir. Y\u00f6ntemin se\u00e7imi, ham maddelerin mevcudiyeti, \u00fcr\u00fcn\u00fcn istenen safl\u0131\u011f\u0131 ve istenen reaksiyon ko\u015fullar\u0131 gibi \u00e7e\u015fitli fakt\u00f6rlere ba\u011fl\u0131 olacakt\u0131r. Bu kimyasallarla \u00e7al\u0131\u015f\u0131rken uygun g\u00fcvenlik protokollerinin ve ekipmanlar\u0131n\u0131n kullan\u0131lmas\u0131 \u00f6nemlidir.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Siklopentanon, C5H8O molek\u00fcler form\u00fcl\u00fcne sahip siklik bir organik bile\u015fiktir. \u00c7e\u015fitli kimyasallar\u0131n sentezinde yayg\u0131n olarak \u00e7\u00f6z\u00fcc\u00fc ve \u00f6nc\u00fc olarak kullan\u0131l\u0131r. IUPAC Ad\u0131 Siklopentanon Molek\u00fcler form\u00fcl C5H8O CAS numaras\u0131 120-92-3 E\u015f anlaml\u0131 Ketosiklopentan, CPK, adipik keton, siklopentanon, ketopentametilen, 1-oksosiklopentan InChI InChI=1S\/C5H8O\/c6-5-3-1-2-4-5\/h1-4H2 Siklopentanonun molar k\u00fctlesi Siklopentanonun molar k\u00fctlesi yakla\u015f\u0131k 84,13 g\/mol&#8217;d\u00fcr. Bu de\u011fer, bile\u015fi\u011fin tek bir molek\u00fcl\u00fcndeki t\u00fcm &#8230; <a title=\"Siklopentanon &#8211; c5h8o, 120-92-3\" class=\"read-more\" href=\"https:\/\/chemuza.org\/tr\/siklopentanon-c5h8o\/\" aria-label=\"More on Siklopentanon &#8211; c5h8o, 120-92-3\">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>Siklopentanon - C5H8O, 120-92-3<\/title>\n<meta name=\"description\" content=\"Siklopentanon, C5H8O molek\u00fcler form\u00fcl\u00fcne sahip siklik bir organik bile\u015fiktir. 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