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Son olarak çözünürlük konusu ele alınıyor ve küçük aldehitler ve ketonların suda çözünür olduğu, ancak zincir uzunluğu arttıkça bu çözünürlük azaldığı belirtiliyor."]},"endTime":693,"title":"Aldehit ve Ketonların Fiziksel Özellikleri","beginTime":0}],"fullResult":[{"index":0,"title":"Aldehit ve Ketonların Adlarının Kökeni","list":{"type":"unordered","items":["Aldehit ve ketonlar, alkolü yükseltme işlemiyle elde edilebilir.","Aldehitlerin ismi \"alkol\" ve \"dehidrojenasyon\" kelimelerinin kısaltmasıdır.","Ketonların ismi, eski Almanca'da \"aketon\" şeklinde yazılan \"aseton\" kelimesinden gelir."]},"beginTime":8,"endTime":128,"href":"/video/preview/7680008693110412281?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=8&ask_summarization=1"},{"index":1,"title":"Moleküller Arası Kuvvetler ve Kaynama Noktaları","list":{"type":"unordered","items":["İzopropanol moleküllerinde hidrojen bağı bulunur ve bu en güçlü moleküller arası kuvvettir.","Aseton moleküllerinde dipol-dipol etkileşimi vardır ve bu hidrojen bağı kadar güçlü değildir.","İzopropanolün kaynama noktası yaklaşık 83°C, asetonun kaynama noktası ise yaklaşık 56°C'dir."]},"beginTime":128,"endTime":362,"href":"/video/preview/7680008693110412281?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=128&ask_summarization=1"},{"index":2,"title":"Farklı Moleküllerin Karşılaştırılması","list":{"type":"unordered","items":["Propan molekülünün kaynama noktası yaklaşık -42°C olduğundan gaz halde bulunur.","Propan'da moleküller arası kuvvetler London dağılım kuvvetleridir.","Propanil (propan aldehiti) molekülünün kaynama noktası yaklaşık 50°C olduğundan sıvı halde bulunur."]},"beginTime":362,"endTime":519,"href":"/video/preview/7680008693110412281?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=362&ask_summarization=1"},{"index":3,"title":"Çözünürlük Özellikleri","list":{"type":"unordered","items":["Aseton molekülünde kutuplaşma (polarlık) durumu vardır ve su molekülüyle hidrojen bağı kurarak suda çözünür.","Küçük aldehitler ve ketonlar nispeten suda çözünür.","Zincirin uzunluğu arttıkça molekül daha apolar hale gelir ve sudaki çözünürlüğü azalır."]},"beginTime":519,"endTime":681,"href":"/video/preview/7680008693110412281?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=519&ask_summarization=1"}],"linkTemplate":"/video/preview/7680008693110412281?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=%%timestamp%%&ask_summarization=1"},"isAdultDoc":false,"relatedParams":{"text":"Aldehitlerin ve Ketonların Fiziksel Özellikleri (Fen Bilimleri) (Organik Kimya)","related_orig_text":"ATP tinhoc-ketoan","related_porno":false,"related_less_3m_off":true,"client":"d2d","no_cnt":1,"related_src":"serp","related":"{\"porno\":false,\"vfp\":1,\"orig_text\":\"ATP 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gün en yeni eğitim videolarını ilk izleyen olmak için kanalımıza abone olun. Daha fazlası ve ders videolarını sıralı izlemek için: https://www.khanacademy.org.tr Matematikten sanat tarihine...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/3444973/3b31c570de753b32822b97dd23f4fdb0/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/aJ7l3QEAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"1","reqid":"1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL","summary":{"isFull":true,"fullTextUrl":"/video/result?ask_summarization=1&numdoc=1&noreask=1&nomisspell=1&parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=videoid:14530768458401389176","teaser":[{"list":{"type":"unordered","items":["Bu video, kimya dersi formatında aldehit ve ketonların nasıl adlandırıldığını anlatan bir eğitim içeriğidir.","Video, önce aldehitlerin yapısını ve adlandırma kurallarını açıklayarak başlıyor, ardından çeşitli aldehit örnekleri (butonal, pentaal, propal, sinemaldehit, benzerldehit, vanilinin) ve bunların IUPAC adlandırma sistemlerini gösteriyor. Daha sonra ketonların yapısı ve adlandırma kuralları ele alınıyor, yeni ve eski adlandırma yöntemleri karşılaştırılıyor.","Videoda ayrıca ketonların çift bağlar, alkil grupları ve halojenler gibi gruplara göre adlandırılması, halkalı moleküllerde ketonların adlandırılması ve aynı molekülde iki keton olduğunda nasıl adlandırılacağı gösterilmektedir. Çift bağların stereokimyasal durumları (trans/e) ve ketonların karbonil karbonlarının adlandırılması da anlatılmaktadır. Laboratuvar araştırmaları için uygun olan bazı aldehitlerin (sinemaldehit, benzerldehit, vanilinin) kokuları da açıklanmaktadır."]},"endTime":848,"title":"Aldehit ve Ketonların Adlandırılması Dersi","beginTime":0}],"fullResult":[{"index":0,"title":"Aldehitlerin Adlandırılması","list":{"type":"unordered","items":["Aldehitlerde bir karbonil grubu (oksijenle çift bağ kurmuş karbon) bulunur ve bir tarafta alkil grubu, diğer tarafta hidrojen vardır.","Aldehitler adlandırılırken karbonil grubuna en küçük sayı verilir ve alkan adının sonuna \"al\" eki eklenir (örneğin, dört karbonlu aldehit butonal).","Aldehit, çift bağlar, ark grupları ve halojenlerden daha önceliklidir."]},"beginTime":6,"endTime":83,"href":"/video/preview/14530768458401389176?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=6&ask_summarization=1"},{"index":1,"title":"Aldehit Örnekleri","list":{"type":"unordered","items":["Beş karbonlu aldehit pentaal olarak adlandırılır ve sübent grubu varsa (örneğin, dört proma pentaal).","Üç karbonlu aldehit propal olarak adlandırılır ve çift bağ varsa propenal olur (örneğin, e-3-fenil-2-propenal veya 3-fenil-2-propenal).","Sinemaldehit (tarçın kokusu veren molekül) ve benzerldehit (badem kokusu veren molekül) özel isimleriyle adlandırılır."]},"beginTime":83,"endTime":316,"href":"/video/preview/14530768458401389176?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=83&ask_summarization=1"},{"index":2,"title":"Vanilin ve Diğer Aldehitler","list":{"type":"unordered","items":["Vanilin molekülü dört hidroksi üç-metoksi benzerldehit olarak adlandırılır ve vanilya kokusunu verir.","Sikloheksa karbaldehit, benzer halkası yerine sikloheksa halkası içeren bir aldehit.","İki aldehit grubu olan moleküller \"-dial\" ekiyle adlandırılır (örneğin, 1,5-pentandiyal veya gluteraldehit)."]},"beginTime":316,"endTime":453,"href":"/video/preview/14530768458401389176?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=316&ask_summarization=1"},{"index":3,"title":"Ketonların Adlandırılması","list":{"type":"unordered","items":["Ketonlarda karbonil grubunun iki tarafta alkil grubu bulunur ve bunlar aynı veya farklı olabilir.","Dört karbonlu keton bütanon olarak adlandırılır (butan kelimesine \"on\" eki eklenir).","Ketonlar ayrıca alkl gruplarına göre de adlandırılabilir (örneğin, metil-etyl keton)."]},"beginTime":453,"endTime":553,"href":"/video/preview/14530768458401389176?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=453&ask_summarization=1"},{"index":4,"title":"Keton Örnekleri","list":{"type":"unordered","items":["Altı karbonlu keton hexxon olarak adlandırılır.","Uzun moleküllerde ketonun konumu önemlidir ve adlandırmada belirtilir (örneğin, 3-hexxon).","Ketonların adlandırılması için hem yeni hem de eski yöntemler kullanılır."]},"beginTime":553,"endTime":592,"href":"/video/preview/14530768458401389176?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=553&ask_summarization=1"},{"index":5,"title":"Ketonların Adlandırılması","list":{"type":"unordered","items":["Yeni yöntemle molekülün adı heksan üç on olarak belirlenebilir, ancak alkil grubuna göre etil propil keton şeklinde de adlandırılabilir.","Ketonların çift bağlar, alkil grupları ve halojenler gibi gruplara göre daha öncelikli olduğu belirtilmiştir.","Ketona en küçük sayıyı vermek için soldan başlanır ve altı karbonlu bir keton heksanon olarak adlandırılır."]},"beginTime":595,"endTime":653,"href":"/video/preview/14530768458401389176?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=595&ask_summarization=1"},{"index":6,"title":"Çift Bağlı Ketonların Adlandırılması","list":{"type":"unordered","items":["Çift bağlı ketonlarda, çift bağ olduğundan hekzaan adı kullanılır ve ketonun konumu belirtilir.","Eski yöntemle molekül e dört heksen iki on şeklinde, yeni yöntemle ise e hekzadı'n-4-en-2-on şeklinde adlandırılabilir.","Çift bağların steryo kimyasında hidrojenlerin zıt taraflarda olduğu ve bunun trans veya e şeklinde ifade edildiği belirtilmiştir."]},"beginTime":653,"endTime":735,"href":"/video/preview/14530768458401389176?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=653&ask_summarization=1"},{"index":7,"title":"Halkalı Ketonların Adlandırılması","list":{"type":"unordered","items":["Halkalı 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İlk bölümde bileşiklerin polar yapısı, dipol-dipol etkileşimleri ve suda çözünürlüğü anlatılırken, ikinci bölümde yanma, katılma, indirgenme ve yükseltme tepkileri ele alınmaktadır. Üçüncü bölümde aldehit ve ketonların genel formülleri ve özellikleri açıklanırken, son bölümde konuyla ilgili soru çözümleri yapılmaktadır.","Videoda ayrıca aldehit ve ketonların parfüm yapımı, anatomik dokuların saklanması ve oje çıkarma gibi kullanım alanları da paylaşılmakta, sınavlarda bu konunun nasıl sorulabileceğine dair ipuçları verilmektedir."]},"endTime":1533,"title":"Aldehit ve Ketonlar Kimya Dersi","beginTime":0}],"fullResult":[{"index":0,"title":"Aldehit ve Ketonların Fiziksel Özellikleri","list":{"type":"unordered","items":["Aldehit ve ketonlar içerdikleri karbon grubu nedeniyle polar maddelerdir.","Polar maddeler dipol-dipol etkileşimlere sahiptir, lon etkileşimleri vardır ve suda çözünür.","Karbon sayısı arttıkça çözünürlük azalır çünkü hidrofobik (su sevmeyen) kısmı artar."]},"beginTime":1,"endTime":77,"href":"/video/preview/14816372129425264347?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=1&ask_summarization=1"},{"index":1,"title":"Aldehit ve Ketonların Moleküler Özellikleri","list":{"type":"unordered","items":["Aldehit ve ketonların moleküller arasında hidrojen bağları yoktur, bu nedenle kaynama noktaları hidrojen bağı yapan moleküllerden daha düşüktür.","Alkanlar sadece London etkileşimlerine sahipken, aldehit ve ketonlar polar maddelerdir.","Aynı karbon sayısında, aldehit ve ketonlar hidrojen bağı yapan moleküllerden daha düşük kaynama noktalarına sahiptir."]},"beginTime":77,"endTime":201,"href":"/video/preview/14816372129425264347?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=77&ask_summarization=1"},{"index":2,"title":"Aldehit ve Ketonların Kimyasal Özellikleri","list":{"type":"unordered","items":["Aldehitler ve ketonlar yanma tepkimesi verirler.","Aldehitler katılmaya tepkime verir, ancak bu bilgi genellikle istenmez.","Aldehitler ve ketonlar indirgenme tepkimesi verirler."]},"beginTime":201,"endTime":317,"href":"/video/preview/14816372129425264347?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=201&ask_summarization=1"},{"index":3,"title":"Aldehit ve Ketonların Özel Tepkimeleri","list":{"type":"unordered","items":["Aldehitler yükseltme tepkimesi verirken, ketonlar yükseltme tepkimesi vermez.","Aldehitler birincil alkole indirgenirken, ketonlar ikincil alkole indirgenir.","Aldehitler polimerleşme tepkimesi verirken, ketonlar vermez (aseton hariç)."]},"beginTime":317,"endTime":472,"href":"/video/preview/14816372129425264347?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=317&ask_summarization=1"},{"index":4,"title":"Alkol Yükseltme ve İndirgenme","list":{"type":"unordered","items":["Birincil (primer) alkoller yükseltme sonucunda aldehit (aldate) oluşturur.","İkincil (sekonder) alkoller yükseltme sonucunda keton oluşturur.","Üçüncül (tersiyer) alkoller yükseltme sonucunda alkolü anlatırken çarpı koyalım, yani yükseltme yapamazlar."]},"beginTime":478,"endTime":540,"href":"/video/preview/14816372129425264347?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=478&ask_summarization=1"},{"index":5,"title":"İndirgenme Tepkimesi","list":{"type":"unordered","items":["Aldehit ve ketonlar indirgenme tepkimesi verir, bu tepkimede karbonhidroksil grubuna hidrojen katılır.","Aldehitlerin indirgenmesi ile primer alkoller, ketonların indirgenmesi ile sekonder alkoller oluşur.","İndirgenme maddeleri olarak lityum, alüminyum hidrür ve sodyum borhidrür yaygın olarak kullanılır."]},"beginTime":540,"endTime":660,"href":"/video/preview/14816372129425264347?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=540&ask_summarization=1"},{"index":6,"title":"Tollen's Test","list":{"type":"unordered","items":["Aldehitler Tollen's test (polense test) ile yükseltme tepkimesi verir ve bu tepkime tanıma tepkimesi olarak bilinir.","Aldehitler Tollen's testte karboksil asit yükseltir ve ortamdaki gümüş iyonları metalik gümüşe indirgenir, bu sonucunda camda gümüş aynası oluşur.","Alkinler Tollen's testte beyaz çökelek oluştururken, aldehitlerde gümüş aynası oluşur."]},"beginTime":660,"endTime":800,"href":"/video/preview/14816372129425264347?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=660&ask_summarization=1"},{"index":7,"title":"Fehling Test","list":{"type":"unordered","items":["Aldehitler Fehling ayracıyla da yükseltme tepkimesi verir ve karboksil asit oluşturur.","Bu tepkimede ortamdaki Cu²⁺ iyonları Cu⁺ iyonlarına indirgenir ve kırmızı renkli bakır bir oksit çökeleği oluşur.","Fehling testinde mavi renkli çözelti rengi çökeleğin renginden dolayı kırmızıya döner."]},"beginTime":800,"endTime":861,"href":"/video/preview/14816372129425264347?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=800&ask_summarization=1"},{"index":8,"title":"Örnek Soru Çözümü","list":{"type":"unordered","items":["Birincil alkoller yükseltme sonucunda aldehit (aldate) oluşturur.","Üçüncül alkoller yükseltme yapamaz, ikincil alkoller ise yükseltme sonucunda keton oluşturur.","Etanol (primer alkol) yükseltme sonucunda aldehit oluşturabilir."]},"beginTime":861,"endTime":999,"href":"/video/preview/14816372129425264347?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=861&ask_summarization=1"},{"index":9,"title":"Aldehit ve Ketonların Kullanım Alanları","list":{"type":"unordered","items":["Aldehit ve ketonlar genellikle hoş kokulu moleküllerdir.","Büyük moleküllü aldehitler parfüm yapımında kullanılır.","Vanilya kokusu veren aldehit bileşiği sin-aldehit, tarçına kokusu veren aldehit ise sin-miş'tir."]},"beginTime":1018,"endTime":1070,"href":"/video/preview/14816372129425264347?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=1018&ask_summarization=1"},{"index":10,"title":"Önemli Aldehit ve Keton Bileşikleri","list":{"type":"unordered","items":["Formaldehitin sulu çözeltisi (formali yüzde otuzyedi'lik) anatomik doku ve organların saklanmasında kullanılır.","Aseton (propoon), ketonların en küçük üyesidir ve reçine, boya ve oje gibi maddeleri çözer.","Aldehit ve ketonlar genel formülü CnH2nO ile gösterilir."]},"beginTime":1070,"endTime":1119,"href":"/video/preview/14816372129425264347?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=1070&ask_summarization=1"},{"index":11,"title":"Aldehit ve Ketonlarla İlgili Rehber Soruları","list":{"type":"unordered","items":["Aldehit ve ketonların ortak özellikleri: karbonhi grubu içerir, genel formülü CnH2nO'dur.","Aldehitler polen ve çözelti etki eder, ketonlar ise bu etkiyi vermez.","Aldehitlerin en küçük üyesi bir karbondur, ketonların en küçük üyesi ise asetondur."]},"beginTime":1119,"endTime":1186,"href":"/video/preview/14816372129425264347?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=1119&ask_summarization=1"},{"index":12,"title":"Aldehit ve Ketonlarla İlgili Örnek Soru Çözümü","list":{"type":"unordered","items":["Bir bileşiğin karbonhi grubu bulundurduğu, amonyaklı gümüşü dat çözeltisi ile tepkime verdiği ve izomeri olan keton bileşiği olmadığı belirtiliyor.","Bir mol bileşiğin yakılması sonucunda 42,80 litre CO2 gazı (2 mol karbondioksit) oluştuğundan, bileşiğin iki karbonlu aldehit olduğu anlaşılıyor.","İki karbonlu aldehitin yaygın adı etanaldır veya aset aldehittir."]},"beginTime":1186,"endTime":1344,"href":"/video/preview/14816372129425264347?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=1186&ask_summarization=1"},{"index":13,"title":"Aldehit ve Ketonlarla İlgili Doğru-Yanlış 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Bileşikler" ünitesine "Aldehit ve Ketonlar" kısmı ile devam ediyoruz. Hepinize kolay gelsin. ⚡ Katıl özelliğini kullanarak ayrıcalıklardan faydalanabilir kanala destek ol...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/1728893/09d1923a2fbd5dd48287b518062ee1ab/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/r2frAgIAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"6","reqid":"1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL","summary":{"isFull":true,"fullTextUrl":"/video/result?ask_summarization=1&numdoc=1&noreask=1&nomisspell=1&parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=videoid:11662705766109112327","teaser":[{"list":{"type":"unordered","items":["Bu video, bir öğretmen tarafından sunulan kimya dersi formatında olup, organik bileşikler ünitesinin devamı niteliğindedir.","Video, karbon bileşiklerinden aldehit ve ketonların detaylı incelemesini içermektedir. İlk olarak karbonil grubu tanıtılarak aldehit ve ketonların yapısal özellikleri, adlandırma kuralları ve izomeri açıklanmakta, ardından sistematik ve yaygın adlandırma yöntemleri örneklerle anlatılmaktadır. Son bölümde ise ketonların genel özellikleri ve ali ketonlar konusu ele alınmaktadır.","Videoda ayrıca simetrik ve asimetrik ketonlar, düz zincirli, halkalı ve aromatik yapılar hakkında bilgiler verilmekte, karbon zincirinin numaralandırılması, bağlı grupların adlandırılması ve karbon grubunun yerinin belirtilmesi gibi konular örneklerle açıklanmaktadır. Dersin sonunda, fiziksel ve kimyasal özelliklerin inceleneceği belirtilmektedir."]},"endTime":1296,"title":"Organik Bileşikler: Aldehit ve Ketonlar Dersi","beginTime":0}],"fullResult":[{"index":0,"title":"Karbon Grubu ve Karbonil Grubu","list":{"type":"unordered","items":["Organik bileşikler ünitesinde karbon bileşiklerinden aldehit ve ketonlar incelenecektir.","Karbon grubu, karbonun çift bağ ile oksijene bağlandığı durumdur ve oksijen üzerinde iki tane eşleşmemiş elektron çifti bulunur.","Karbon grubunu içeren bileşikler polar olup, karbon grubu ile oksijen arasındaki bağ açısı 120 derecedir."]},"beginTime":11,"endTime":55,"href":"/video/preview/11662705766109112327?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=11&ask_summarization=1"},{"index":1,"title":"Karbonil Grubu İçeren Bileşikler","list":{"type":"unordered","items":["Karbon grubunu içeren dört tane bileşik vardır: aldehit, keton, karboksilik asit ve eserler.","Aldehitte karbon grubundaki karbon bir tarafına hidrojen, diğer tarafına radikal veya hidrojen bağlanabilir.","Ketonda karbon grubundaki karbonun her iki tarafına radikal bağlı olmak zorundadır.","Karboksilik asitte karbon grubundaki karbonun bir tarafına OH grubu, diğer tarafı ise radikal ve hidrojen bağlanır.","Eserde karbon grubunun bir tarafı oksijen, diğer tarafı radikal olur."]},"beginTime":55,"endTime":132,"href":"/video/preview/11662705766109112327?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=55&ask_summarization=1"},{"index":2,"title":"Aldehit ve Ketonların Özellikleri","list":{"type":"unordered","items":["Aldehit, karbonil grubundaki karbona bir tane hidrojen bağlanmasıyla oluşan organik bileşiklerdir.","Ketonlar, karbonil grubundaki karbonun her iki tarafına da radikal bağlanmasıyla oluşan organik bileşiklerdir.","Aldehitlerin fonksiyonel grubu COOH kalıbıdır, ketonların fonksiyonel grubu ise C grubu (C=O) kalıbıdır.","Aldehitlerde karbonil grubunun bir tarafında hidrojen varsa aldehit, her iki tarafında radikal varsa ketondur."]},"beginTime":132,"endTime":208,"href":"/video/preview/11662705766109112327?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=132&ask_summarization=1"},{"index":3,"title":"Aldehit ve Ketonların Adlandırılması","list":{"type":"unordered","items":["Aldehitlerin adlandırması, karbonil grubunun ilk iki harfi ile yapılır (etanal, propanal).","Ketonların adlandırması, karbonil grubunun sonundaki \"on\" ile yapılır (propanon, butanon).","Aldehitlerde simetrik veya asimetrik durum yoktur, ancak ketonlarda karbonil grubunun her iki tarafında aynı radikal grup varsa basit (simetrik), farklı gruplar varsa asimetrik (karışık) keton olarak sınıflandırılır.","Aldehit ve ketonlar düz zincirli olabilecekleri gibi halkalı ya da aromatik yapıda da olabilirler."]},"beginTime":208,"endTime":362,"href":"/video/preview/11662705766109112327?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=208&ask_summarization=1"},{"index":4,"title":"Aldehit ve Ketonların İzomerliği","list":{"type":"unordered","items":["Aldehit ve ketonların molekül formülleri aynı (CnH2nO) olduğundan, karbon sayıları aynıysa birbirinin yapı izomeridir.","Aldehit ve ketonların izomerliği fonksiyonel grup izomerliğidir.","Karbon sayıları eşit olduğu durumda aldehit ve ketonlar birbirinin izomeridir.","Benzer şekilde karboksilik asit ve eserler de karbon sayıları eşit olduğu durumda birbirinin izomeridir."]},"beginTime":362,"endTime":443,"href":"/video/preview/11662705766109112327?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=362&ask_summarization=1"},{"index":5,"title":"Aldehit ve Ketonların Sistematik Adlandırılması","list":{"type":"unordered","items":["Aldehitlerin sistematik adlandırması (IUPAC adlandırması) için öncelikle karbon grubu içeren en uzun karbon zinciri seçilir.","Karbonil grubu en küçük rakamı alacak şekilde numaralandırılır.","Önce bağlı gruplar adlandırılır, sonra ana zincirdeki karbon sayısına karşılık gelen hidrokarbon adının sonuna \"aldehit\" eki getirilerek adlandırılır.","Aldehit bir numarasını almak zorunda olduğu için aldehitlerin yeri belirtilmez, ancak ketonlarda yer belirtilir."]},"beginTime":443,"endTime":521,"href":"/video/preview/11662705766109112327?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=443&ask_summarization=1"},{"index":6,"title":"Aldehitlerin Adlandırılması","list":{"type":"unordered","items":["Aldehitlerin adlandırılmasında önce organik bileşiğin ne olduğuna (alkollü, eter, aldehit, keto) karar verilir.","Aldehit kalıbında tek karbon bulunur ve karbon grubunun bağlı olduğu karbona bağlı grup olarak değerlendirilir.","Tek karbonlu aldehit metanal (formaldehit), iki karbonlu aldehit etanal (aset aldehit), üç karbonlu aldehit propal (propiyon aldehit) olarak adlandırılır."]},"beginTime":528,"endTime":678,"href":"/video/preview/11662705766109112327?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=528&ask_summarization=1"},{"index":7,"title":"Ketonların Adlandırılması","list":{"type":"unordered","items":["Ketonların adlandırmasında aldehitlerden farklı olarak karbon grubunun yeri belirtilir.","Ketonlarda karbon grubu mutlaka bir numaralı karbona bağlı olmak zorunda değildir, iki, üç veya dört numaralı karbona da bağlanabilir.","Üç ve dört karbonlu ketonlarda karbon grubu farklı konumlarda yazılamayacağı için yeri belirtilmesine gerek yoktur."]},"beginTime":678,"endTime":845,"href":"/video/preview/11662705766109112327?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=678&ask_summarization=1"},{"index":8,"title":"Sistematik ve Yaygın Adlandırma","list":{"type":"unordered","items":["Sistematik adlandırmada karbon grubuna bağlı radikal grupların adları sırasıyla alfabetik sıraya göre okunur ve sonra \"keton\" getirilir.","Yaygın adlandırmada karbon grubunun her iki tarafına bağlanan radikallerin adları alfabetik sıraya göre yazılır ve sonra \"keton\" getirilir.","Karbon grubunun her iki tarafına aynı radikal bağlandığında (örneğin iki metil veya iki fenil) \"dimetil keton\" veya \"difenil keton\" şeklinde 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VE Ketonlar Fiziksel Özellikleri VE Eldesi 1. Aldehit VE Ketonlarin Fiziksel Özellikleri 2. Aldehitlerin Sentezleri 1° Alkollerin Yükseltgenmesiyle Aldehit Eldesi Açil Klorürlerden Aldehit...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/2975071/f4409968a257c1d5b5e5c3bd6d39eab8/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/A-UMGAIAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"10","reqid":"1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL","summary":{"isFull":true,"fullTextUrl":"/video/result?ask_summarization=1&numdoc=1&noreask=1&nomisspell=1&parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=videoid:9558464476607805482","teaser":[{"list":{"type":"unordered","items":["Bu video, Üniversite Kimyası YouTube kanalından bir kimya dersidir. Eğitmen, aldehit ve ketonların fiziksel özellikleri ve sentez yöntemlerini anlatmaktadır.","Video, aldehit ve ketonların karbonil grubu nedeniyle hidrokarbonlardan daha yüksek kaynama noktasına sahip olduğunu açıklayarak başlıyor. Ardından bu moleküllerin suda çözünürlüğü ve doğal kaynaklardan elde edilen aromatik aldehitler (vanilya, sinema dehit) hakkında bilgi veriliyor. Son bölümde ise aldehitlerin sentez yöntemleri detaylı olarak anlatılıyor: alkollerin yükseltgenmesi ve açil klorürlerden aldehit eldesi. Özellikle açil klorürlerden aldehit eldesi için lityum triter botoksi alüminyum hidrür kullanılarak gerçekleştirilen reaksiyonun mekanizması adım adım gösteriliyor."]},"endTime":488,"title":"Aldehit ve Ketonların Fiziksel Özellikleri ve Sentez Yöntemleri","beginTime":0}],"fullResult":[{"index":0,"title":"Aldehit ve Ketonların Fiziksel Özellikleri","list":{"type":"unordered","items":["Aldehit ve ketonlar, karbonil grubu polar bir gruptur ve bu nedenle aynı molekül kütleli hidrokarbonlardan daha yüksek kaynama noktasına sahiptir.","Aldehit ve ketonlar hidrojen bağı oluşturamazlar, bu nedenle kaynama noktaları alkollere göre daha düşüktür.","Karbonil grubundaki oksijen atomu sayesinde aldehit ve ketonlar su molekülleri ile kuvvetli hidrojen bağları yapabilirler ve düşük molekül kütleli olanları suda iyi 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Yayınları AYT Kimya Konu Özetli Soru Bankası Bölüm 10 - Test 7 | Ayt Soru Çözüm Kampı | 2022 ⚡ Katıl özelliğini kullanarak ayrıcalıklardan faydalanabilir kanala destek olabilirsiniz...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/4034012/7aea111c75168b0785287d935ab1c0cf/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/9bdU7gEAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"12","reqid":"1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL","summary":{"isFull":true,"fullTextUrl":"/video/result?ask_summarization=1&numdoc=1&noreask=1&nomisspell=1&parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=videoid:10758579748448548924","teaser":[{"list":{"type":"unordered","items":["Bu video, bir eğitmenin kimya dersinde aldehit ve ketonlar konusunu anlattığı eğitim içeriğidir.","Videoda aldehit ve ketonların moleküler yapıları, genel formülleri, kaynama noktaları, tepkimeleri ve izomeri gibi konular ele alınmaktadır. Eğitmen, soru-cevap formatında ilerleyerek bileşiklerin yapılarını çizerek açıklamakta ve doğru cevapları belirtmektedir.","Video ayrıca aldehit ve ketonların yükseltgenme-indirgenme tepkimeleri, polimerleşme özellikleri, Tollens çözeltisi ile tepkimeleri ve gümüş aynası oluşturma gibi konuları da kapsamaktadır. Öğrencilere bu konudaki kavramları pekiştirmeleri için örnekler sunulmaktadır."]},"endTime":761,"title":"Aldehit ve Ketonlar Kimya Dersi","beginTime":0}],"fullResult":[{"index":0,"title":"Aldehit ve Ketonların Ortak Özellikleri","list":{"type":"unordered","items":["Aldehit ve ketonlar karbon, hidrojen ve oksijen içerdiği için polar yapıdadırlar.","Hem aldehit hem keton suyun rengini gidermez.","Hem aldehit hem ketonda karbon grubu (karbonat çift bağlı oksijen) bulunur."]},"beginTime":5,"endTime":32,"href":"/video/preview/10758579748448548924?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=5&ask_summarization=1"},{"index":1,"title":"Karbon Sayıları Eşit Bileşiklerin Kaynama Noktaları","list":{"type":"unordered","items":["Karbon sayıları eşit olan eter, keton ve aldehit bileşiklerinde moleküller arasında dipol-dipol etkileşim vardır.","Ketonun kaynama noktası en büyük, daha sonra aldehitin, en son eterin kaynama noktasıdır."]},"beginTime":32,"endTime":68,"href":"/video/preview/10758579748448548924?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=32&ask_summarization=1"},{"index":2,"title":"Keton ve Aldehit İndirgenme Tepkimeleri","list":{"type":"unordered","items":["Keton indirgendiğinde sekonder alkol oluşur.","Aldehit indirgendiğinde primer alkol oluşur.","Üç karbonlu bir keton indirgendiğinde CH₃-COOH (sekonder alkol) ve CH₃-CH₂-OH (propanol) oluşur.","X ve Y birbirinin yapı izomeridir çünkü kapalı formülleri aynı ancak açık yapıları farklıdır."]},"beginTime":68,"endTime":147,"href":"/video/preview/10758579748448548924?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=68&ask_summarization=1"},{"index":3,"title":"Aldehit ve Ketonların Polimerleşme Tepkimesi","list":{"type":"unordered","items":["Aldehitler polimerleşme tepkimesi verirken, ketonlar normalde polimerleşme tepkimesi vermez.","Aseton (dimetil keton) polimerleşme tepkimesi verir.","Aldehitler fenol çözeltisi yükseltebilirken, ketonlar yükseltgenme tepkisi vermez çünkü karbona bağlı hidrojen yoktur.","Aldehitler indirgen özellik gösterirken, ketonlar indirgen özellik göstermez."]},"beginTime":147,"endTime":214,"href":"/video/preview/10758579748448548924?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=147&ask_summarization=1"},{"index":4,"title":"Aldehit Tanıma","list":{"type":"unordered","items":["Genel formülü CnH2nO olan ve Tollens çözeltisi ile gümüş aynası oluşturan bir bileşik aldehittir.","Karboksilik asit, keton, alkol ve eter Tollens çözeltisi ile gümüş aynası oluşturmaz."]},"beginTime":214,"endTime":243,"href":"/video/preview/10758579748448548924?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=214&ask_summarization=1"},{"index":5,"title":"Asetaldehit Elde Edilme Yöntemleri","list":{"type":"unordered","items":["Asetaldehit (etilen) iki karbonlu bir aldehittir.","İki karbonlu primer alkol yükseltildiğinde asetaldehit elde edilir.","İki karbonlu karboksilik asit indirgendiğinde asetaldehit elde edilir.","Alkenler su ile tepkimede alkol elde edilir, asetaldehit elde edilmez."]},"beginTime":243,"endTime":294,"href":"/video/preview/10758579748448548924?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=243&ask_summarization=1"},{"index":6,"title":"Asetilen ve Asetaldehit Tepkimesi","list":{"type":"unordered","items":["Kalsiyum-karbon suyla tepkimesinden asetilen (C₂H₂) elde edilir.","Asetilen suyla tepkimede enol-keto tauto merisi sonucunda asetaldehit elde edilir."]},"beginTime":294,"endTime":375,"href":"/video/preview/10758579748448548924?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=294&ask_summarization=1"},{"index":7,"title":"Aldehit ve Ketonların Karşılaştırılması","list":{"type":"unordered","items":["Primer alkol yükseltildiğinde aldehit elde edilir.","Sekonder alkol yükseltildiğinde keton elde edilir.","Aldehitler ve ketonlar birbirinin fonksiyonel grup izomerisidir.","Aldehitler Tollens çözeltisi etki ederken, ketonlar etki etmez.","Her ikisi de brom suyun rengini gidermez."]},"beginTime":375,"endTime":457,"href":"/video/preview/10758579748448548924?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=375&ask_summarization=1"},{"index":8,"title":"Aldehit Yükseltme Tepkimesi Hesaplaması","list":{"type":"unordered","items":["13,20 gram aldehit yükseltilmesiyle 64,80 gram metalik gümüş oluşur.","Gümüşün mol kütlesi 108 gram/mol olduğundan, 64,80 gram gümüş 0,60 mol'dur.","Aldehit yükseltme tepkimesinde katsayı oranı 1:2 olduğundan, 0,60 mol aldehit 0,30 mol karbonat gerektirir."]},"beginTime":457,"endTime":496,"href":"/video/preview/10758579748448548924?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=457&ask_summarization=1"},{"index":9,"title":"Aletin Kütlesi ve Molekül Yapısı","list":{"type":"unordered","items":["Aletin kütlesi verilmiş ve aletin genel formülü C₂H₄O olarak belirlenmiştir.","Aletin mol kütlesi 13,20 mol/kg olarak hesaplanmıştır.","Aletin molekül yapısında iki tane karbon atomu olduğu tespit edilmiştir."]},"beginTime":506,"endTime":561,"href":"/video/preview/10758579748448548924?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=506&ask_summarization=1"},{"index":10,"title":"Aseton ve Aset Halden Karışımı Problemi","list":{"type":"unordered","items":["Aseton ve aset halden oluşan karışımın iki mol molekül içerdiği belirtilmiştir.","Karışımın yeterli miktar fa çözeltiden geçirilmesiyle 72 gram bakır oksit çökeleği oluşmuştur.","Aseton keton olduğu için fa çözeltisi ile tepkimeye girmez, sadece aset halden (C₂H₄O) çözer ve yükseltilir.","Karışımın %75'i aseton olduğu hesaplanmıştır."]},"beginTime":561,"endTime":673,"href":"/video/preview/10758579748448548924?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=561&ask_summarization=1"},{"index":11,"title":"Fonksiyonel Grup İzomeri","list":{"type":"unordered","items":["Aynı karbon sayılı aldehit ve ketonlar birbirinin fonksiyonel grup izomeridir.","Tek karbonlu formaldehit izomeri olan bir keton yoktur.","İki karbonlu aset halden izomeri olan bir keton yoktur, ancak propain izomeri 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Eğitmen önce karbon bileşikleri başlığının dördüncü konusu olan ketonları tanıtarak, karbonil grubunun yapısını ve ketonların aldehitlerden nasıl farklılaştığını açıklamaktadır. Ketonların simetrik ve asimetrik olarak sınıflandırılması, izomeri ve genel özellikleri detaylı olarak anlatılmaktadır. Video, ikinci bölümde adlandırmalar ve fiziksel-kimyasal özelliklerin işleneceği bilgisiyle sonlanmaktadır."]},"endTime":588,"title":"Ketonlar Dersi","beginTime":0}],"fullResult":[{"index":0,"title":"Yeni Seriler ve Ketonlar","list":{"type":"unordered","items":["Keton, asit, ester ve k ile ders videoları bitiriliyor, ancak yılbaşından sonra yeni serilere başlanacak.","Geçen sene başlanan \"üç soru bir konu\" serisi baştan başlatılacak ve bu sene \"ÖSYM'nin en sık sorduğu on soru\" serisi başlatılacak.","Ketonlar son on yılda çıkan tüm organik soruların yüzde on iki'sini oluşturuyor ve geçen sene ketonlardan soru çıkmamış."]},"beginTime":0,"endTime":91,"href":"/video/preview/16713042147434603882?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=0&ask_summarization=1"},{"index":1,"title":"Karbonil Grubu ve Karbon Bileşikleri","list":{"type":"unordered","items":["Karbonil grubu, karbona çift bağlı oksijen bağlandığında elde 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Eğitmen, koruyucu gruplar konusunun asetaller kısmını anlatmaktadır.","Video, asetallerin sulu asitlerde aldehitlere ve ketonlara hidroliz olmasına rağmen bazik çözeltilerde kararlı olduğunu açıklayarak başlıyor. Ardından asetallerin aldehit ve ketonları koruma amacıyla nasıl kullanılabileceği örneklerle gösteriliyor. Daha sonra tiyo asetaller, Raney nikeli ve bu grupların hidrokarbon elde etmek için nasıl kullanıldığı anlatılıyor. Video, sikloheksanın tolene dönüştürülmesi ve benzaldehitin tolene dönüştürülmesi gibi örneklerle sonlanıyor."]},"endTime":632,"title":"Asetaller ve Koruyucu Gruplar Dersi","beginTime":0}],"fullResult":[{"index":0,"title":"Asetaller ve Koruyucu Özellikleri","list":{"type":"unordered","items":["Asetaller sulu asit içerisinde aldehitlere ve ketonlara hidroliz olmalarına rağmen bazik çözeltilerde kararlıdırlar ve hidroliz olmazlar.","Asetaller, adet ve keton grupları bazik çözeltilerde istenmeyen tepkimelerden korumak için kullanılabilir.","Asetal grubu (O-R ve O-R) su varlığında ve bazik ortamda tepkime vermez, hidroliz olmaz."]},"beginTime":4,"endTime":73,"href":"/video/preview/9189030677702615442?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=4&ask_summarization=1"},{"index":1,"title":"Asetaller Kullanımı Örnekleri","list":{"type":"unordered","items":["Ketonları korumak için asit ortamda asetale çevirmek gerekir, böylece ketonlar korunur ve sadece esterler indirgenir.","Green reaktifi kullanarak OH-CH3 grubunu elde etmek için de asetale dönüştürme işlemi yapılır.","Asetale dönüştürme işlemi, ketonları koruyarak istenen ürünleri elde etmeyi sağlar."]},"beginTime":73,"endTime":313,"href":"/video/preview/9189030677702615442?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=73&ask_summarization=1"},{"index":2,"title":"Tiyo-asetaller","list":{"type":"unordered","items":["Tiyo-asetaller, adet ve ketonlar tiyollerle tepkimeye girerek elde edilebilir.","Tiyo-asetaller, karbon atomuna bağlı kükürt ve üstü grubu içerir.","Halkalı tiyo-asetaller, bor-tri-florür kullanılarak elde edilebilir."]},"beginTime":313,"endTime":421,"href":"/video/preview/9189030677702615442?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=313&ask_summarization=1"},{"index":3,"title":"Raney Nikeli ve Hidrojenleme","list":{"type":"unordered","items":["Raney nikeli, hidrojen içeren özel bir nikel katalizörüdür.","Raney nikeli kullanılarak tiyo-asetaller hidrokarbona dönüştürülebilir.","Klemensen indirgenmesi ve amalgamlanmış çinko ile de aldehit ve ketonlar hidrokarbona dönüştürülebilir."]},"beginTime":421,"endTime":516,"href":"/video/preview/9189030677702615442?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=421&ask_summarization=1"},{"index":4,"title":"Örnek Uygulamalar","list":{"type":"unordered","items":["Siklo-hegzaon ketonu, tiyo-asetale dönüştürülüp Raney nikeli ile hidrojenlenerek siklo-hekzana dönüştürülebilir.","Benzaldehit, tiyo-asetale dönüştürülüp Raney nikeli ile hidrojenlenerek hidrokarbona dönüştürülebilir.","Bu reaksiyonlar, aldehit ve ketonları hidrokarbona dönüştürmek için önemli yöntemlerdir."]},"beginTime":516,"endTime":631,"href":"/video/preview/9189030677702615442?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=516&ask_summarization=1"}],"linkTemplate":"/video/preview/9189030677702615442?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=%%timestamp%%&ask_summarization=1"},"isAdultDoc":false,"relatedParams":{"text":"Organik kimya |aldehit ve ketonlar | koruyucu gruplar olarak asetaller","related_orig_text":"ATP tinhoc-ketoan","related_porno":false,"related_less_3m_off":true,"client":"d2d","no_cnt":1,"related_src":"serp","related":"{\"porno\":false,\"vfp\":1,\"orig_text\":\"ATP 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#KimyaAdası 👇TÜM Siniflar İÇİN Oynatma Listeleri👇 📽AYT Kimya Oynatma Listesi: https://bit.ly/36w7l3m 📽TYT Kimya Oynatma Listesi: https://bit.ly/357rVFQ 📽12. Sınıf Kimya Oynatma...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/3215693/c9401a4ef0d826f35475a292fea72766/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/QrR4gAEAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"16","reqid":"1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL","summary":{"isFull":true,"fullTextUrl":"/video/result?ask_summarization=1&numdoc=1&noreask=1&nomisspell=1&parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=videoid:14167294976995419431","teaser":[{"list":{"type":"unordered","items":["\"Kimyadası\" ders kanalında yayınlanan bu eğitim videosunda, bir öğretmen organik kimyada aldehitler ve ketonlar konusunu detaylı şekilde anlatmaktadır.","Video, aldehitler ve ketonların genel özellikleri, yapıları ve isimlendirilmesi üzerine odaklanmaktadır. İlk olarak bu bileşiklerin karbonil yapısı ve aldehit ile keton arasındaki farklar açıklanmakta, ardından sistematik adlandırma kuralları (UPAK sistemi) örneklerle gösterilmektedir. Daha sonra yapı formüllerinin nasıl yazılacağı ve izomeri konuları ele alınmakta, son bölümde ise AYT soru bankasından test soruları çözülmektedir.","Videoda ayrıca aldehitlerin ve ketonların fonksiyonel grup izomerleri olduğu, izomer sayısının karbon sayısına göre nasıl arttığı ve yedi karbonlu bir aldehit veya keton bileşikinin genel yapısı gibi konular da işlenmektedir. Dersin sonunda, bir sonraki derste bu bileşiklerin tepkimelerinin konuşulacağı belirtilmektedir."]},"endTime":1790,"title":"Organik Kimyada Aldehitler ve Ketonlar Dersi","beginTime":0}],"fullResult":[{"index":0,"title":"Aldehitler ve Ketonlar Tanıtımı","list":{"type":"unordered","items":["Organik kimyada aldehitler ve ketonlar önemli bir kısım olup, kazanımlar fazla olduğu için iki bölüme ayrılmıştır.","Aldehitler ve ketonlar karbonil grubu içeren bileşiklerdir ve genel formülü CnH2nO şeklindedir.","Karbonil grubu bir numaralı karbonda ise aldehit, karbon zincirinin içerisindeyse keton olarak adlandırılır."]},"beginTime":0,"endTime":85,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=0&ask_summarization=1"},{"index":1,"title":"Aldehit ve Ketonların Yapısı","list":{"type":"unordered","items":["Aldehit yapısında karbonil grubuna hidrojen bağlandığında, keton yapısında ise başka bir karbon grubu bağlanır.","Ketonlarda R1 ve R2 grupları aynı ise simetrik keton, farklı ise asimetrik keton olarak adlandırılır.","En basit yapılı aldehit bir karbonludur (CH2O), en basit yapılı keton ise üç karbonludur (C3H6O)."]},"beginTime":85,"endTime":314,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=85&ask_summarization=1"},{"index":2,"title":"Aldehit ve Ketonların Özellikleri","list":{"type":"unordered","items":["Aldehitler ve ketonlar polar yapıya sahip oldukları için suda çözünürler.","Kendi aralarında hidrojen bağı oluşturamazlar çünkü hidrojenle karbon bağ yaparlar, ancak suyla çözündüklerinde hidrojen bağı oluşturabilirler.","Aynı karbon sayısına sahip olan aldehitler ve ketonlar birbirlerinin fonksiyonel grup izomeridir."]},"beginTime":314,"endTime":405,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=314&ask_summarization=1"},{"index":3,"title":"İzomerler","list":{"type":"unordered","items":["Bir numaralı ve iki numaralı aldehitlerin izomeri yoktur çünkü keton olamazlar.","Karbon sayısı arttıkça izomer sayısı da artar.","Aynı karbon sayısına sahip aldehit ve ketonlar aynı kapalı formüllere sahip olabilir ancak açık formülleri farklıdır."]},"beginTime":405,"endTime":549,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=405&ask_summarization=1"},{"index":4,"title":"Aldehitlerin Sistematik Adlandırılması","list":{"type":"unordered","items":["Aldehitlerin sistematik adlandırması (UPAK sistemi) yapılırken öncelikle en uzun karbon zinciri belirlenir.","Karbon grubu (aldehit grubu) bir nolu olacak şekilde numaralandırılır ve yan gruplar (metil, etil vb.) önce belirtilir.","Karbon sayısına karşılık gelen alkan ismi (metan, etan, propan vb.) ve \"al\" eki eklenerek aldehit ismi oluşturulur."]},"beginTime":553,"endTime":631,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=553&ask_summarization=1"},{"index":5,"title":"Aldehitlerin Özel İsimleri","list":{"type":"unordered","items":["İki karbonlu aldehit \"etanal\" olarak adlandırılır ve özel ismi \"asetaldehit\" (sirke asidi) olarak da bilinir.","Dallanmış aldehitlerde karbon grubunun numarası belirtilir, örneğin \"2-metilpropanal\".","Çok karbonlu aldehitlerde karbon grubunun numarası belirtilir ve yan gruplar (metil, etil vb.) numaralandırılır, örneğin \"3,4-trimetilpentanal\"."]},"beginTime":631,"endTime":757,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=631&ask_summarization=1"},{"index":6,"title":"Karmaşık Aldehitlerin Adlandırılması","list":{"type":"unordered","items":["Hem aldehit hem de alken özelliği gösteren bileşiklerde, en uzun karbon zinciri belirlenir ve karbon grubunun numarası belirtilir.","Yan gruplar (metil, etil vb.) numaralandırılır ve alken grubu belirtilir, örneğin \"5-etil-4-hexenal\".","Benzen halkasına bağlı aldehit \"benzaldehit\" olarak adlandırılır."]},"beginTime":757,"endTime":870,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=757&ask_summarization=1"},{"index":7,"title":"Özel Aldehitlerin İsimleri","list":{"type":"unordered","items":["Tek karbonlu aldehit \"metanal\" olarak adlandırılır ve özel ismi \"formaldehit\" olarak da bilinir.","İki karbonlu aldehit \"butadial\" olarak adlandırılır ve iki aldehit grubu olduğunu gösterir.","Siglo bütan (tek zincirli alkan) üzerine aldehit bağlandığında \"butanal\" olarak adlandırılır."]},"beginTime":870,"endTime":991,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=870&ask_summarization=1"},{"index":8,"title":"Ketonların Adlandırılması","list":{"type":"unordered","items":["Ketonların adlandırması UPAK sistemine göre yapılır, ancak \"al\" yerine \"on\" eki kullanılır.","Ketonların yaygın isimlendirmesinde önce alkil isimleri söylenir, sonra \"keton\" kelimesi eklenir, örneğin \"dimetilketon\".","Üç karbonlu keton \"propanon\" olarak adlandırılır ve yaygın ismi \"aseton\" olarak bilinir."]},"beginTime":991,"endTime":1110,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=991&ask_summarization=1"},{"index":9,"title":"Ketonların İsimlendirilmesi","list":{"type":"unordered","items":["Metil en-propil keton, karbonhid grubunun bir karbondan bağlı olduğu için bu şekilde isimlendirilir.","Dört dört dimetil hexanon, en uzun karbon zincirinde dört metil grubu bulunan bir keton örneğidir.","Siglobutanon, siglobutanın hidrojenlerinin oksijenle değiştirilmesiyle elde edilen bir keton türüdür."]},"beginTime":1114,"endTime":1191,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=1114&ask_summarization=1"},{"index":10,"title":"Aromatik Ketonlar","list":{"type":"unordered","items":["Fenil siglohexil keton, benzenin kapalı formundan bir hidrojen çıkarılıp fenil grubu eklenerek elde edilen bir keton türüdür.","Ketonların isimlendirilmesinde karbonhid grubunun konumu ve bağlı olduğu gruplar önemlidir.","Ketonların formüllerini bulmak için en uzun karbon zinciri belirlenir ve bağlı gruplar numaralandırılır."]},"beginTime":1191,"endTime":1320,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=1191&ask_summarization=1"},{"index":11,"title":"Özel Keton Türleri","list":{"type":"unordered","items":["Allil keton, propen (C₃H₆) yapısından bir hidrojen çıkarılıp C₂H₄ yapısı elde edilerek oluşturulur.","Vinil keton, etilen (C₂H₄) yapısından bir hidrojen çıkarılıp C₂H₃ yapısı elde edilerek oluşturulur.","Büta diyon, dört karbonlu bir yapıda iki karbonhid grubu bulunan bir keton türüdür."]},"beginTime":1320,"endTime":1441,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=1320&ask_summarization=1"},{"index":12,"title":"Aldehitlerin Özellikleri","list":{"type":"unordered","items":["Aldehitler bir karbon içerir, nötrdür ve aynı karbon sayılı ketonlarla izomerdir.","Karbon sayısı arttıkça aldehitlerin kaynama noktası artarken sudaki çözünürlükleri azalır.","Aldehitler kendi içerisinde hidrojen bağı içermez."]},"beginTime":1441,"endTime":1479,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=1441&ask_summarization=1"},{"index":13,"title":"Aldehit ve Keton Örnekleri","list":{"type":"unordered","items":["C₂H₄ yapısında X=H ve Y=H olduğunda en basit yapılı aldehit olan metanal (formaldehit) elde edilir.","C₃H₈ yapısında X=C₂H₅ ve Y=C₂H₄ olduğunda etil-metil keton (bütanon) elde edilir.","C₃H₈ yapısında X=C₂H₄ ve Y=C₂H₄ olduğunda dimetil keton (propanon veya aseton) elde edilir.","C₂H₄ yapısında X=H ve Y=C₃H₈ olduğunda etanal (asetaldehit) elde edilir."]},"beginTime":1479,"endTime":1561,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=1479&ask_summarization=1"},{"index":14,"title":"Aromatik Aldehit ve İzomerler","list":{"type":"unordered","items":["Benzen aldehit, benzenin (C₆H₆) yapısından bir hidrojen çıkarılıp aldehit grubu bağlanarak elde edilir.","Siklopentanon, C₅H₁₀ yapısından bir karbon çiftli bağ yaparak C₅H₈ yapısına dönüşür.","Benzen aldehit ve siklopentanon izomer değildir çünkü kapalı formülleri farklıdır (C₇H₆O ve C₅H₈O).","Aldehitler indirgenler ve hidrojenle katılma tepkimesi verirler."]},"beginTime":1561,"endTime":1663,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=1561&ask_summarization=1"},{"index":15,"title":"Bileşik Sorusu Çözümü","list":{"type":"unordered","items":["Soruda genel yapısı verilmiş bir bileşikle ilgili \"hangisi olamaz\" sorusu sorulmuştur.","Bileşik yedi karbonlu bir aldehit veya asimetrik bir keton olmalıdır.","Asimetrik keton olması için karbonhid grubu içerde olmalıdır."]},"beginTime":1665,"endTime":1700,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=1665&ask_summarization=1"},{"index":16,"title":"Seçeneklerin İncelenmesi","list":{"type":"unordered","items":["İlk seçenek (CH₃) yedi karbonlu bir keton olup asimetrik olduğu için doğru cevaptır.","İkinci seçenek (C₂H₅ ve C₃H₇) altı karbonlu bir aldehit olup asimetrik olduğu için doğru cevaptır.","Üçüncü seçenek (C₃H₇) yedi karbonlu bir aldehit olup asimetrik olmadığı için doğru cevaptır."]},"beginTime":1700,"endTime":1764,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=1700&ask_summarization=1"},{"index":17,"title":"Dersin Sonu","list":{"type":"unordered","items":["Ders uzun tutulmuş ancak daha fazla uygulama yapabilmek ve daha iyi anlamak için bu çalışma yapılmıştır.","Bir sonraki derste bu bileşiklerin tepkimeleri konuşulacaktır.","Öğrencilere güzel günler ve bol kimya netli günler dilenmiştir."]},"beginTime":1764,"endTime":1790,"href":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=1764&ask_summarization=1"}],"linkTemplate":"/video/preview/14167294976995419431?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=%%timestamp%%&ask_summarization=1"},"isAdultDoc":false,"relatedParams":{"text":"Z24 - Aldehit VE Ketonlar - 1. 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Kanala katıl, hem videolara erken eriş hem de her ay piyasada olmayan 10 kimya denemesi çöz. Fehling-Tollens deney videosu: • Using Tollens' Reagent to Test for...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/4372668/302ca342f4d658bf750d0ff24d43357e/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/uA4b6AEAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"17","reqid":"1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL","summary":{"isFull":true,"fullTextUrl":"/video/result?ask_summarization=1&numdoc=1&noreask=1&nomisspell=1&parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=videoid:13266526621294474693","teaser":[{"list":{"type":"unordered","items":["Bu video, bir öğretmenin organik kimya dersinde aldehit ve ketonlar konusunu anlattığı eğitim içeriğidir.","Videoda aldehit ve ketonların polar yapısı, kaynama noktaları, yükseltme ve indirgenme tepkimeleri detaylı şekilde ele alınmaktadır. Öğretmen, bu bileşiklerin kimyasal özellikleri arasındaki farkları, Fehling-Tollens ayracıyla gümüş aynası oluşturma özelliğini ve çeşitli aldehitlerin (formaldehit, temel, benzen, aseton) kullanım alanlarını açıklamaktadır.","Video, konunun üç video ile hızlıca halledildiğini belirterek ve soru çözümleriyle sonlanmaktadır. Ayrıca polifonksiyonel bileşikler ve aldehitlerin gümüş nitratla tepkimesi gibi konular da videoda yer almaktadır."]},"endTime":985,"title":"Aldehit ve Ketonların Fiziksel ve Kimyasal Özellikleri","beginTime":0}],"fullResult":[{"index":0,"title":"Aldehit ve Ketonların Fiziksel Özellikleri","list":{"type":"unordered","items":["Aldehit ve ketonlar yapısındaki oksijenden dolayı polar yapılıdır ve dipol-dipol taşırlar.","Kaynama noktası hidrokarbonlardan yüksektir ancak alkollerden düşüktür çünkü alkollerde hidrojen bağı taşır.","Karbon sayısı arttıkça kaynama noktası artar ancak molekül büyüyeceği için çözünürlük azalır."]},"beginTime":0,"endTime":51,"href":"/video/preview/13266526621294474693?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=0&ask_summarization=1"},{"index":1,"title":"Aldehit ve Ketonların Yükseltme ve İndirgenme Özellikleri","list":{"type":"unordered","items":["Yükseltme, bir maddenin oksijen alması veya hidrojen vermesidir; indirgenme ise bir maddenin hidrojen alması veya oksijen vermesidir.","Aldehitlerin yükseltmesi oksijen alma, indirgenmesi ise hidrojen alma ile gerçekleşir.","Ketonlar yükseltmez çünkü hidrojen içermezler, indirgenirken hidrojen katılır."]},"beginTime":51,"endTime":141,"href":"/video/preview/13266526621294474693?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=51&ask_summarization=1"},{"index":2,"title":"Yükseltme ve İndirgenme Örnekleri","list":{"type":"unordered","items":["Primer alkol yükseltmez, sekonder alkol yükseltirken iki hidrojeni silip piba bekler.","Aldehit yükseltirken araya oksijen eklenir, karboksilik asit yükseltmez.","Karboksilik asit indirgerken eklenen oksijen silinir, aldehit indirgerken hidrojen katılır."]},"beginTime":141,"endTime":472,"href":"/video/preview/13266526621294474693?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=141&ask_summarization=1"},{"index":3,"title":"Aldehit ve Ketonların Tepkimeleri","list":{"type":"unordered","items":["Aldehitlerin ikinci önemli tepkimesi Fehling-Tollens ayracına indirgen olarak etki etmeleridir.","Aldehitler Fehling-Tollens ayracıyla yükseltilirken ayracını indirgerler.","Ketonlar bu tepkiyi vermez çünkü kendileri yükseltmez ve karşıdaki maddeyi indirgeyemezler."]},"beginTime":472,"endTime":540,"href":"/video/preview/13266526621294474693?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=472&ask_summarization=1"},{"index":4,"title":"Fehling-Tollens Ayracı Tepkimesi","list":{"type":"unordered","items":["Aldehitler Fehling-Tollens ayracıyla tepkimede bir oksijen gelip yükseltir, gümüş metalik gümüşe indirgenir.","Asetilen de bu tepkimeye etki eder ancak oluşan organik tuz çökerse indirgenen metal çöker.","Aldehitler gümüşle gümüş aynası oluştururken, alkinler beyaz çökelek oluşturur."]},"beginTime":540,"endTime":631,"href":"/video/preview/13266526621294474693?parent-reqid=1765349686430207-9673629944260603672-balancer-l7leveler-kubr-yp-vla-180-BAL&text=ATP+tinhoc-ketoan&t=540&ask_summarization=1"},{"index":5,"title":"Aldehit Fonksiyonel Grubu Testi","list":{"type":"unordered","items":["Aldehit fonksiyonel grubu içeren maddeler, şeffaf suya konulduğunda ısıtıldığında ayna görüntüsü oluşturur.","Alkinlerle aynı test yapıldığında, kabın dibinde beyaz bir çökelek oluşur.","Polifonksiyonel bileşikler hem alken hem aldehit grubu içerir ve bu bileşikler hem alkenlerin hem de aldehitlerin özelliklerini 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