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[À¯±âÈÇнÇÇè2 A£«]Labreport10 Synthesis of Photochromic dye / 1. Results 2. Discussion / 1. Results À̹ø ½ÇÇè¿¡¼´Â Æ÷ÅäÅ©·Î¹Í ¿°·áÀÇ ÇÕ¼ºÀ» ¸ñÇ¥·Î ÇÏ¿´°í, ½ÇÁ¦ ÇÕ¼º ÀÌÈÄ¿¡´Â ¹ÝÀÀ °á°ú¿Í »ý¼ºµÈ ÈÇÕ¹°ÀÇ Æ¯¼ºÀ» ºÐ¼®ÇÏ¿´´Ù. ÇÕ¼ºÀÌ ¿Ï·áµÈ ÈÄ, »ý¼ºµÈ Æ÷ÅäÅ©·Î¹Í ¿°·áÀÇ ¹°Áú Ư¼ºÀ» Æò°¡Çϱâ À§ÇØ ´Ù¾çÇÑ ¹æ¹ýÀ» »ç¿ëÇÏ¿´´Ù. ¸ÕÀú, ÇÕ¼ºµÈ ÈÇÕ¹°ÀÇ ¼øµµ¸¦ È®ÀÎÇϱ⡦ |
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[À¯±âÈÇнÇÇè2 A£«]Labreport2 bromination of stilbene / 1. Results 2. Discussion / 1. Results ½ÇÇèÀÇ °á°ú ºÎºÐ¿¡¼´Â ½ºÆ¿º¥ÀÇ ºê·Î¹ÎÈ ¹ÝÀÀÀ» ÅëÇØ »ý¼ºµÈ ºê·Î¸ð½ºÆ¿º¥ÀÇ ¼öÀ²°ú ±¸Á¶Àû Ư¼ºÀ» ´Ù·é´Ù. º» ½ÇÇè¿¡¼ ½ºÆ¿º¥°ú ºê·Î¹ÎÀ» ¹ÝÀÀ½ÃÄÑ ºê·Î¸ð½ºÆ¿º¥À» ÇÕ¼ºÇÏ¿´´Ù. ½ÇÇè ÈÄ, ¹ÝÀÀ¹°°ú »ý¼º¹°ÀÇ È®ÀÎÀ» À§ÇØ °¢ ¹°ÁúÀÇ ºÐ±¤ÇÐÀû ºÐ¼®À» ½Ç½ÃÇÏ¿´´Ù. ½ºÆ¿º¥Àº ¹ÝÀÀ ¡¦ |
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[À¯±âÈÇнÇÇè2 A£«]Labreprot5 Synthesis of stilbene using a wittig reaction / 1. Results 2. Discussion / 1. Results À̹ø ½ÇÇèÀÇ °á°ú·Î ¾ò¾îÁø ¹°ÁúÀº ½ºÆ¿º¥(Styrene)À̸ç, ÀÌ´Â À¸®È÷ ¹ÝÀÀ(Wittig reaction)À» ÅëÇØ ÇÕ¼ºµÇ¾ú´Ù. ÇÕ¼º °úÁ¤¿¡¼ »ç¿ëµÈ Àü±¸Ã¼´Â Æ÷½ºÆ÷´½ ¿°(Ph3P=CHÀ¸·Î, ÀÌ ¹ÝÀÀÀº ¾Ëµ¥ÇÏÀ̵峪 ÄÉÅæ°ú ¹ÝÀÀÇÏ¿© ÀÌÁß °áÇÕÀ» °¡Áø ¾ËÄËÀ» »ý¼ºÇϴ ģÀüÀÚ¡¦ |
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[À¯±âÈÇнÇÇè2 A£«]Labreport6 Synthesis fo stilbene Olefin metathesis / 1. Results 2. Discussion / 1. Results Synthesis of stilbene through olefin metathesis resulted in a series of interesting observations and findings. The reaction commenced with the mixing of the starting materials, which included a suitable alkene substrate and the appropriate catal¡¦ |
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[À¯±âÈÇнÇÇè2 A£«]Labreport8,9 Suzuki-Miyaura Cross-Coupling Biaryl / 1. Results 2. Discussion / 1. Results º» ½ÇÇè¿¡¼´Â Suzuki-Miyaura ±³Â÷ °áÇÕ ¹ÝÀÀÀ» ÅëÇØ ºñ¾Æ¸± ÈÇÕ¹°À» ÇÕ¼ºÇÏ¿´´Ù. ÀÌ ¹ÝÀÀÀº ÁÖ·Î ÇҷΰÏÈ ¾Æ¸±°ú º¸·Ð»êÀ» ¹ÝÀÀ½ÃÄÑ »õ·Î¿î ¾Æ¸± °áÇÕÀ» Çü¼ºÇÏ´Â °úÁ¤À¸·Î, Çö´ë À¯±âÈÇп¡¼ Áß¿äÇÑ ÇÕ¼º ¹æ¹ý Áß ÇϳªÀÌ´Ù. ½ÇÇè¿¡ »ç¿ëµÈ ¾Æ¸± ÇÒ¶óÀÌµå ¹× º¸¡¦ |
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[À¯±âÈÇнÇÇè2 A£«]Labreport3 Diels-Alder reaction(1,3-butadiene£«maleic anhydride) / 1. Results 2. Discussion / 1. Results Diels-Alder ¹ÝÀÀÀ» ÅëÇØ 1,3-butadiene°ú maleic anhydrideÀÇ °áÇÕÀÌ ÀÌ·ç¾îÁø °á°ú¸¦ ºÐ¼®ÇÑ °ÍÀÌ´Ù. ½ÇÇè¿¡¼ »ç¿ëµÈ 1,3-butadieneÀº ºÒ¾ÈÁ¤ÇÑ ÈÇÕ¹°·Î, ¹ÝÀÀ Á¶°Ç¿¡ µû¶ó ½±°Ô ÁßÇÕÇÒ ¼ö ÀÖ´Ù´Â Á¡¿¡¼ ÁÖÀÇ°¡ ÇÊ¿äÇß´Ù. ÀÌ ¶§¹®¿¡ ½ÇÇè °úÁ¤¿¡¡¦ |
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[À¯±âÈÇнÇÇè2 A£«]Labreport7 Synthesis of stilbene triphenylcarbinol-grignard reaction / 1. Results 2. Discussion / 1. Results À̹ø ½ÇÇè¿¡¼´Â ½ºÆ¿º¥°ú Æ®¸®Æä´ÒÄ«¸£ºñ³îÀÇ ÇÕ¼ºÀ» ¸ñÇ¥·Î ÇÏ¿© ±×¸®³Ä¸£ ¹ÝÀÀÀ» ¼öÇàÇÏ¿´´Ù. ½ÇÇè °á°ú, ¹ÝÀÀ¿¡¼ ¸ñÇ¥ »ý¼º¹°À» ¼º°øÀûÀ¸·Î ÇÕ¼ºÇÏ¿´À¸¸ç, »ý¼º¹°ÀÇ ¼øµµ¿Í ¼öÀ²À» È®ÀÎÇÏ¿´´Ù. ½ºÆ¿º¥À» »ý¼ºÇϱâ À§ÇØ ¸ÕÀú º¥Áú ºê·Î¸¶À̵塦 |
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[À¯±âÈÇнÇÇè2 A£«]Labreport1 Carbocation rearrangements-benzopinacolone / 1. Results 2. Discussion / 1. Results ½ÇÇè °úÁ¤¿¡¼ ¾òÀº °á°úµéÀº ´ÙÀ½°ú °°´Ù. benzopinacoloneÀÇ ÇÕ¼º °úÁ¤¿¡¼ óÀ½¿¡ °üÂûÇÑ °ÍÀº ¹ÝÀÀÀÌ ÁøÇàµÇ¸é¼ »ý¼º¹°ÀÇ ¹°¸®Àû ¼ºÁú¿¡ ´ëÇÑ º¯È¿´´Ù. óÀ½ »ç¿ëÇÑ ¹ÝÀÀ¹°ÀÎ benzoinÀº À¯±â ¿ë¸Å¿Í È¥ÇÕµÇ¸é¼ ÃʱâÀÇ °íü »óÅ¿¡¼ ¼¼È÷ ¿ëÇصǴ Ư¡¡¦ |
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(labreport)1. Carbocation Rearrangements-Benzopinacolone / 1. Results 2. Discussion / 1. Results ½ÇÇè °á°ú´Â º¥Á¶ÇÉÄ®·ÐÀÇ Ä«º¹ÀÌ¼Ç Àç¹è¿¿¡ ´ëÇÑ ½Éµµ ÀÖ´Â ÀÌÇظ¦ Á¦°øÇÑ´Ù. ½ÇÇèÀº º¥Á¶ÇÉÄ®·ÐÀÇ ÇÕ¼ºÀ» À§ÇÑ ¹ÝÀÀ ¸ÞÄ¿´ÏÁòÀ» ºÐ¼®ÇÏ´Â µ¥ ÁßÁ¡À» µÎ¾ú´Ù. ¹ÝÀÀ ¸ÞÄ¿´ÏÁòÀº ÁÖ·Î Ä«º¹À̼ÇÀÇ Çü¼º°ú Àç¹è¿ °úÁ¤À» Æ÷ÇÔÇÑ´Ù. °á°úÀûÀ¸·Î °üÂûµÈ Ä«º¹À̼ÇÀÇ ¾ÈÁ¤¼ºÀº ½ÇÇè¿¡¼¡¦ |
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(prelab,¿¹ºñ,labreport,°á°ú)7. Triphenylcarbinol-Grignard Reaction / 1. Objectives 2. Principles & Methods 3. Table of relevant chemical properties 4. Results 5. Discussion / 1. Objectives Triphenylcarbinol-Grignard ReactionÀÇ ¸ñÀûÀº À¯±âÇÕ¼º¿¡¼ Áß¿äÇÑ ¿ªÇÒÀ» ÇÏ´Â ±×¸®³Ä¸£ ½Ã¾àÀ» ÀÌ¿ëÇÏ¿© »ïÆä´Ò Ä«¸£ºñ³îÀ» ÇÕ¼ºÇÏ´Â °ÍÀÌ´Ù. ÀÌ ¹ÝÀÀÀº À¯±â ÈÇÕ¹°ÀÇ ±â¡¦ |
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