compounds °Ë»ö°á°ú
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Èֹ߼º À¯±âÈÇÕ¹°ÀÇ Á¤ÀÇ¿Í Æ¯Â¡¿¡ ´ëÇؼ ÀÛ¼ºÇß½À´Ï´Ù. [±³¾ç]Èֹ߼ºÀ¯±âÈÇÕ¹° / (1) ÁÖÁ¦ ¼±Á¤ ÀÌÀ¯. (2) Á¤ ÀÇ. (VOC ; Volatile Organic Compounds) (3) Ư ¡. (VOC ; Volatile Organic Compounds) / (3) Ư ¡. (VOC ; Volatile Organic Compounds) Èֹ߼ºÀ¯±âÈÇÕ¹°(VOC)Àº °íÁ¤¹èÃâ¿ø¿¡¼ÀÇ À¯±â¿ëÁ¦ »ç¿ë°ú ¾×ü¿¬·áÀÇ »ç¿ë, ¼ö¼Û, ÀúÀå ¹× ÀÚµ¿Â÷ µî À̵¿¹èÃâ¿ø¿¡¼ »ç¡¦ |
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À¯±âÈÇÕ¹°ÀÇ Á¾·ù¿Í IUPAC(International Union of Pure and Applied Chemistry) ±Ô¾à ¹× ´ëÇÑÈÇÐȸ¿¡¼ Á¤ÇÑ ±ÔÄ¢¿¡ ÀÇÇÑ ¸í¸í¹ýÀ» Á¤¸®Çß½À´Ï´Ù. ¿©·¯ºÐµé¿¡°Ô ¸ðÂÉ·Ï µµ¿òÀÌ ÀÖÀ¸¸®¶ó »ý°¢µÇ¸ç, ´Ùµé A+ ¹ÞÀ¸½Ã±æ ¹Ù¶ø´Ï´Ù. ~ À¯±âÈÇÕ¹° ¸í¸í¹ý / (1) ¾ËÄÉÀÎÀÇ(alkane)ÀÇ ¸í¸í¹ý ¢º¾Ëų±â(alkyl group) (2) ÇҷΰÕÈ ¾Ëų(alkyl halide) (3) »çÀÌŬ·Î¾ËÄÉÀÎ(cycloalkane) (4) ¾Ë¡¦ |
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À¯±â ÀÛ¿ë±â(Functional Graoup Idevfication of Organic Compounds by the Use of Chemical Reaction) ¿¹ºñ / 1. ½ÇÇè¸ñÀû 2. ÀÌ·Ð 3. ½ÇÇèÀåÄ¡ ¹× ½Ã¾à 4. ½ÇÇè¹æ¹ý 5. Ãß·Ð / 1. ½ÇÇè¸ñÀû À̹ø ½ÇÇèÀÇ ¸ñÀûÀº À¯±â ÈÇÕ¹°¿¡¼ ƯÁ¤ À¯±â ÀÛ¿ë±â¸¦ È®ÀÎÇÏ°í ½Äº°ÇÏ´Â µ¥ ÀÖ´Ù. À¯±â ÈÇÕ¹°Àº ±× ±¸Á¶¿Í ¼ºÁú¿¡ µû¶ó ´Ù¾çÇÏ°Ô ºÐ·ùµÉ ¼ö ÀÖÀ¸¸ç, ÀÌ·¯ÇÑ ºÐ·ùÀÇ Áß¿äÇÑ ±âÁØ Áß ÇÏ¡¦ |
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À¯±âÀÛ¿ë±â(Functional Graoup Idevfication of Organic Compounds by the Use of Chemical Reaction) °á°ú / 1. ½ÇÇè¹æ¹ý 2. ³íÀÇ ¹× °íÂû / 1. ½ÇÇè¹æ¹ý À¯±âÀÛ¿ë±â ½Äº°À» À§ÇÑ ½ÇÇè¹æ¹ýÀº ÈÇÕ¹°ÀÇ ±â´ÉÀû Ư¼ºÀ» ÀÌÇØÇÏ°í ºÐ¼®ÇÏ´Â µ¥ ÁßÁ¡À» µÐ´Ù. ½ÇÇèÀº ´Ù¾çÇÑ À¯±â ÈÇÕ¹°À» ÁغñÇÏ°í, ÀÌµé °¢°¢¿¡ ´ëÇØ Æ¯Á¤ ÈÇÐ ¹ÝÀÀÀ» ¼öÇàÇÏ¿© À¯±âÀÛ¿ë±â¸¦ ½Äº°ÇÏ´Â ¹æ½ÄÀ¸·Î ÁøÇàµÈ´Ù¡¦ |
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1.Benzene º¥Á¨Àº ´ëÇ¥ÀûÀÎ ¹æÇâÁ· ÈÇÕ¹°·Î, C6H6ÀÇ ÈÇнÄÀ» °¡Áø´Ù. º¥Á¨Àº ±¸Á¶ÀûÀ¸·Î °í¸® ÇüÅÂÀÇ Åº¼Ò ¿øÀÚ 6°³°¡ ¼·Î °áÇÕÇØ .. / 1.Benzene 2.Aromatic Compounds 3.Reactions at the Benzylic Position 4.Reduction of Benzene and Its Derivatives 5.Spectroscopy of Aromatic Compounds / 1.Benzene º¥Á¨Àº ´ëÇ¥ÀûÀÎ ¹æÇâÁ· ÈÇÕ¹°·Î, C6H6ÀÇ ÈÇнÄÀ» °¡Áø´Ù. º¥Á¨¡¦ |
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1. Introduction À¯±â ÈÇÕ¹°ÀÇ »êÈ ¹ÝÀÀÀº ÈÇп¡¼ Áß¿äÇÑ ÁÖÁ¦ Áß Çϳª·Î, ´Ù¾çÇÑ »ýÈÇÐÀû °úÁ¤°ú »ê¾÷Àû ÀÀ¿ë¿¡ ÇʼöÀûÀÎ ¿ªÇÒÀ».. / 1. Introduction 2. Reaction Scheme & Procedure 3. Results 4. Discussion 5. Conclusion 6. Reference / 1. Introduction À¯±â ÈÇÕ¹°ÀÇ »êÈ ¹ÝÀÀÀº ÈÇп¡¼ Áß¿äÇÑ ÁÖÁ¦ Áß Çϳª·Î, ´Ù¾çÇÑ »ýÈÇÐÀû °úÁ¤°ú »ê¾÷Àû ÀÀ¿ë¿¡ ÇʼöÀûÀΡ¦ |
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À¯±âÇÕ¼º½ÇÇè 2. Reduction of Carbonyl compounds - Preparation of Alcohols °á°úº¸°í¼ / 1. ½ÇÇè¸ñÀû 2. ½ÇÇè¹æ¹ý 3. ½ÇÇè°á°ú ¹× ºÐ¼® 4. °íÂû / 1. ½ÇÇè¸ñÀû À¯±âÇÕ¼º ½ÇÇèÀÇ ÀÏȯÀ¸·Î ź¼Òyl ÈÇÕ¹°ÀÇ È¯¿ø ¹ÝÀÀÀ» ÅëÇØ ¾ËÄÚ¿ÃÀ» ÇÕ¼ºÇÏ´Â ½ÇÇèÀÇ ¸ñÀûÀº À¯±â ÈÇп¡¼ Áß¿äÇÑ ¹ÝÀÀ Áß ÇϳªÀΠȯ¿ø ¹ÝÀÀ¿¡ ´ëÇÑ ÀÌÇظ¦ ³ôÀÌ°í, À̸¦ ÅëÇØ À¯±â ÈÇÕ¹°ÀÇ ±¸Á¶¿Í ¼ºÁú »çÀÌÀÇ¡¦ |
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À¯±âÇÕ¼º½ÇÇè 2. Reduction of Carbonyl Compounds- Preparation of Alcohols / 1. ½ÇÇè ¸ñÀû 2. ½ÇÇè ÀÌ·Ð 1)ȯ¿ø 2)reduction of alkene 3)reduction of alkyne 4)reduction of carbonyl compound 5)ȯ¿øÁ¦ 6)acetophenone ȯ¿ø mechanism 7)styrene 8)TLC 3. ½ÇÇè ¹æ¹ý 4. ½Ã¾àÁ¶»ç 5. Âü°í¹®Çå / 1. ½ÇÇè ¸ñÀû À¯±âÇÕ¼º½ÇÇè 2ÀÇ ¸ñÀûÀº Ä«º¸´Ò ÈÇÕ¹°À» ȯ¿øÇÏ¿©¡¦ |
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