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- Á¦ 4° 2Àå À¯±âºÐÀÚÀÇ Æ¯Â¡ - ÀüÀڹеµ ÆÇ´Ü¿¡¼ºÎÅÍ ÇÏÀÌÆÛÄÁÁê°ÔÀ̼Ç(¥ò ⇆ p)±îÁö [¼ö¾÷ÀÏ : 03/10] 45ºÐ
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- 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 ÀÔüÈÇÐ - chiralityºÎÅÍ ¿ë¾îÁ¤¸®±îÁö [¼ö¾÷ÀÏ : 03/17] 32ºÐ
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- 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 ¿¡Æø½ÃȹÝÀÀ±îÁö [¼ö¾÷ÀÏ : 03/24] 41ºÐ
- Á¦ 17° 7Àå Alkene - ´ÙÀÌ¿Ã »ý¼ººÎÅÍ ¾ËÄËÀÇ »êȼº ºÐÇعÝÀÀ±îÁö [¼ö¾÷ÀÏ : 03/24] 31ºÐ
- Á¦ 18° 8Àå Alkyne - ¸í¸í¹ýºÎÅÍ ¼öȹÝÀÀ±îÁö [¼ö¾÷ÀÏ : 03/24] 48ºÐ
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- 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
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- 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
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- 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
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