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[2019´ëºñ] [¹Ú»óÀÏ] À¯±âÈ­ÇÐ ½ÉÈ­¹Ý (3-4¿ù)

[2019´ëºñ] [¹Ú»óÀÏ] À¯±âÈ­ÇÐ ½ÉÈ­¹Ý (3-4¿ù)

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    • [2019´ëºñ] [¹Ú»óÀÏ] À¯±âÈ­ÇÐ ½ÉÈ­¹Ý (3-4¿ù)
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  • Á¦ 1°­ ¿À¸®¿£Å×À̼Ç, 1Àå ±¸Á¶¿Í °áÇÕ - ÀüÀÚ¹èÄ¡¿Í ±âº»°³³ä [¼ö¾÷ÀÏ : 03/09] 65ºÐ
  • Á¦ 2°­ 1Àå ±¸Á¶¿Í °áÇÕ - È¥¼º¿ÀºñÅ»ºÎÅÍ ±¸Á¶½Ä±îÁö [¼ö¾÷ÀÏ : 03/09] 57ºÐ
  • Á¦ 3°­ 2Àå À¯±âºÐÀÚÀÇ Æ¯Â¡ - ½Ö±ØÀÚ¸ð¸àÆ®¿¡¼­ °ø¸í±îÁö[¼ö¾÷ÀÏ : 03/10] 51ºÐ
  • Á¦ 4°­ 2Àå À¯±âºÐÀÚÀÇ Æ¯Â¡ - ÀüÀڹеµ ÆÇ´Ü¿¡¼­ºÎÅÍ ÇÏÀÌÆÛÄÁÁê°ÔÀ̼Ç(¥ò ⇆ p)±îÁö [¼ö¾÷ÀÏ : 03/10] 45ºÐ
  • Á¦ 5°­ 2Àå À¯±âºÐÀÚÀÇ Æ¯Â¡ - ÇÏÀÌÆÛÄÁÁê°ÔÀ̼Ç(¥ò ⇆ ¥ò*)¼³¸í [¼ö¾÷ÀÏ : 03/10] 14ºÐ
  • Á¦ 6°­ 2Àå À¯±âºÐÀÚÀÇ Æ¯Â¡ - ÄÁÁê°ÔÀ̼ǺÎÅÍ pKa°ª°ú »êÀÇ ¼¼±â±îÁö[¼ö¾÷ÀÏ : 03/17] 48ºÐ
  • Á¦ 7°­ 2Àå À¯±âºÐÀÚÀÇ Æ¯Â¡ - ºÐÀÚ±¸Á¶¿Í »ê¼ºµµºÎÅÍ ²ú´ÂÁ¡ ³ì´ÂÁ¡ºñ±³±îÁö [¼ö¾÷ÀÏ : 03/17] 46ºÐ
  • Á¦ 8°­ 3Àå Alkane - ÀÛ¿ë±âºÎÅÍ ÇüÅÂÀ̼ºÁúÇö»ó±îÁö[¼ö¾÷ÀÏ : 03/17] 42ºÐ
  • Á¦ 9°­ 4Àå Cycloalkane - ¸í¸í¹ýºÎÅÍ CyclohexaneÀÇ Æ¯Â¡±îÁö[¼ö¾÷ÀÏ : 03/17] 44ºÐ
  • Á¦ 10°­ 4Àå Cycloalkane - CyclohexaneÀÇ Æ¯Â¡ºÎÅÍ ¿©·¯°í¸®È­ÇÕ¹°±îÁö [¼ö¾÷ÀÏ : 03/17] 53ºÐ
  • Á¦ 11°­ 5Àå ÀÔüȭÇÐ - chiralityºÎÅÍ ¿ë¾îÁ¤¸®±îÁö [¼ö¾÷ÀÏ : 03/17] 32ºÐ
  • Á¦ 12°­ 6Àå À¯±â¹ÝÀÀÀÇ °³¿ä - ¹ÝÀÀÁ¾·ùºÎÅÍ Çϸóµå°¡¼³±îÁö[¼ö¾÷ÀÏ : 03/23] 37ºÐ
  • Á¦ 13°­ 7Àå Alkene - ¸í¸í¹ýºÎÅÍ Ä£ÀüÀÚü Á¾·ù±îÁö[¼ö¾÷ÀÏ : 03/23] 46ºÐ
  • Á¦ 14°­ 7Àå Alkene - Ä£ÀüÀÚ¼º ¾ç¼ºÀÚ Ã·°¡¹ÝÀÀºÎÅÍ Åº¼Ò¾çÀÌ¿ÂÀç¹è¿­±îÁö[¼ö¾÷ÀÏ : 03/23] 44ºÐ
  • Á¦ 15°­ 7Àå Alkene - ¼öÀº Ä£ÀüÀÚü, ÇÒ·ÎÁ¨ Ä£ÀüÀÚü [¼ö¾÷ÀÏ : 03/24] 43ºÐ
  • Á¦ 16°­ 7Àå Alkene - carbene÷°¡ºÎÅÍ ¿¡Æø½ÃÈ­¹ÝÀÀ±îÁö [¼ö¾÷ÀÏ : 03/24] 41ºÐ
  • Á¦ 17°­ 7Àå Alkene - ´ÙÀÌ¿Ã »ý¼ººÎÅÍ ¾ËÄËÀÇ »êÈ­¼º ºÐÇعÝÀÀ±îÁö [¼ö¾÷ÀÏ : 03/24] 31ºÐ
  • Á¦ 18°­ 8Àå Alkyne - ¸í¸í¹ýºÎÅÍ ¼öÈ­¹ÝÀÀ±îÁö [¼ö¾÷ÀÏ : 03/24] 48ºÐ
  • Á¦ 19°­ 8Àå Alkyne - ÇÒ·ÎÁ¨Ã·°¡ºÎÅÍ 9Àå Alkylhalide - ¶óµðĮ÷°¡¹ÝÀÀ±îÁö [¼ö¾÷ÀÏ : 03/24] 41ºÐ
  • Á¦ 20°­ 9Àå Alkylhalide - AllylÀÚ¸® ¶óµðĮġȯºÎÅÍ ¾ËÄÝÀ» ÀÌ¿ëÇÑ Á¦¹ý±îÁö [¼ö¾÷ÀÏ : 03/24] 28ºÐ
  • Á¦ 21°­ 9Àå Alkylhalide - À¯±â±Ý¼Ó½Ã¾àºÎÅÍ SN2¹ÝÀÀ±îÁö [¼ö¾÷ÀÏ : 04/06] 40ºÐ
  • Á¦ 22°­ 9Àå Alkylhalide - SN1¹ÝÀÀºÎÅÍ E2Á¦°Å¹ÝÀÀ±îÁö [¼ö¾÷ÀÏ : 04/06] 47ºÐ
  • Á¦ 23°­ 9Àå Alkylhalide - E1Á¦°Å¹ÝÀÀºÎÅÍ ¿ë¸ÅÈ¿°ú±îÁö[¼ö¾÷ÀÏ : 04/06] 56ºÐ
  • Á¦ 24°­ 10Àå Conjugated systems - ´ÙÀÌ¿£ Á¾·ùºÎÅÍ ÀüÀÚ°í¸®È­¹ÝÀÀ±îÁö [¼ö¾÷ÀÏ : 04/07] 50ºÐ
  • Á¦ 25°­ 10Àå Conjugated systems - Diels_Alder¹ÝÀÀºÎÅÍ 11Àå ¹æÇâÁ·È­ÇÕ¹° - ºñ¹æÇâÁ·¼º±îÁö [¼ö¾÷ÀÏ : 04/07] 45ºÐ
  • Á¦ 26°­ 11Àå ¹æÇâÁ·È­ÇÕ¹° - ¹æÇâÁ·ÅºÈ­¼ö¼ÒºÎÅÍ ¿©·¯°í¸®¹æÇâÁ·±îÁö [¼ö¾÷ÀÏ : 04/07] 32ºÐ
  • Á¦ 27°­ 11Àå ¹æÇâÁ·È­ÇÕ¹° - Ä£ÀüÀÚ¼º¹æÇâÁ·Ä¡È¯ºÎÅÍ EWGÈ¿°ú±îÁö [¼ö¾÷ÀÏ : 04/13] 49ºÐ
  • Á¦ 28°­ 11Àå ¹æÇâÁ·È­ÇÕ¹° - EWG, o-, p-¹èÇâºÎÅÍ º¥Á¨ °ç»ç½½¹ÝÀÀ±îÁö [¼ö¾÷ÀÏ : 04/13] 47ºÐ
  • Á¦ 29°­ 12Àå Alcohol, Ether - ¸í¸í¹ýºÎÅÍ ¿°±â¼ºÁ¶°Ç¿¡¼­ Å»¼ö¹ÝÀÀ±îÁö [¼ö¾÷ÀÏ : 04/13] 37ºÐ
  • Á¦ 30°­ 12Àå Alcohol, Ether - ÇdzªÄÝÀç¹è¿­ºÎÅÍ EtherÀÇ »ê¼ººÐÇرîÁö [¼ö¾÷ÀÏ : 04/14] 40ºÐ
  • Á¦ 31°­ 12Àå Alcohol, Ether - Claisen Àç¹è¿­ºÎÅÍ 13Àå Carbonyl È­ÇÕ¹° - Nitrile÷°¡±îÁö[¼ö¾÷ÀÏ : 04/14] 46ºÐ
  • Á¦ 32°­ 13Àå Carbonyl È­ÇÕ¹° - Amine÷°¡ºÎÅÍ Cannizzaro ¹ÝÀÀ±îÁö [¼ö¾÷ÀÏ : 04/14] 47ºÐ
  • Á¦ 33°­ 13Àå Carbonyl È­ÇÕ¹° - Baeyer-Villiger oxidationºÎÅÍ 14Àå Carboxylic acid, Nitrile-Hell-Volhard-Zelinski reaction±îÁö[¼ö¾÷ÀÏ : 04/20] 46ºÐ
  • Á¦ 34°­ 14Àå Carboxylic acid, Nitrile-Nitrile Á¦¹ýºÎÅÍ 16Àå ¥á-Substitution ±îÁö [¼ö¾÷ÀÏ : 04/20] 46ºÐ
  • Á¦ 35°­ 16Àå ¥á-Substitution ¥á-AlkylationºÎÅÍ Ester¿Í Ketone, NitrileÀÇ ¥á-Alkylation ±îÁö [¼ö¾÷ÀÏ : 04/20] 31ºÐ
  • Á¦ 36°­ 17Àå Condensation-Aldol reactionºÎÅÍ Cross-Claisen Condensation±îÁö [¼ö¾÷ÀÏ : 04/21] 42ºÐ
  • Á¦ 37°­ 17Àå Condensation-Diekmann-Condensation ºÎÅÍ Stork reaction±îÁö[¼ö¾÷ÀÏ : 04/21] 16ºÐ
  • Á¦ 38°­ 18Àå Amine Á¦¹ý ºÎÅÍ Diazo coupling±îÁö [¼ö¾÷ÀÏ : 04/27] ¡ÚÁ¾°­¡Ú 48ºÐ
  • Á¦ 39°­ 11°­¿¡¼­ 12°­ »çÀÌÀÇ º¸Ãæ°­ÀÇÀÔ´Ï´Ù.[¼ö¾÷ÀÏ:09/10] 45ºÐ

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