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È­ÇаøÇÐ - Reduction of chlorobenzaldehyde with NaBH4 [À¯±âÇÕ¼º]

È­ÇаøÇÐ - Reduction of chlorobenzaldehyde with NaBH4 [À¯±âÇÕ¼º]

È­ÇаøÇÐ - Reduction of chlorobenzaldehyde with NaBH4 [À¯±âÇÕ¼º] / È­ÇаøÇÐ - Reduction of chlorobenzaldehyde with NaBH4 1. ½ÇÇè ¿ä¾à À̹ø½ÇÇèÀº 2-chlorobenzaldehyde¸¦ NaBH4¿Í ¹ÝÀÀ½ÃÄÑ 2-chlorobenzyl alchoholÀ» »ý¼º½ÃÅ°´Â ȯ¿ø¹ÝÀÀÀÌ´Ù.NaBH4´Â ¾Ëµ¥ÇÏÀ̵å¿Í ÄÉÅæÀ» ¼±ÅÃÀûÀ¸·Î ȯ¿ø½ÃÅ°´Â ȯ¿øÁ¦ÀÌ´Ù. ÀÌ ¶§ ¿ë¸Å·Î´Â ¿¡Åº¿ÃÀ» »ç¿ëÇÑ´Ù. ¾Ëµ¥ÇÏÀ̵åÀÇ Åº¼Ò¾çÀ̿¿¡ ¡¦
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Reduction ¿¹ºñº¸°í¼­

Reduction ¿¹ºñº¸°í¼­

Reduction ¿¹ºñº¸°í¼­ / 1. ½ÇÇèÁ¦¸ñ 2. ½ÇÇè¸ñÀû 3. ½ÇÇèÀÌ·Ð 4. ½ÇÇè¹æ¹ý 5. ½Ã¾àÁ¶»ç 6. Âü°í¹®Çå / 1. ½ÇÇèÁ¦¸ñ ½ÇÇè Á¦¸ñÀº `ReductionÀÇ ÀÌÇØ ¹× ¸ÞÄ¿´ÏÁò Ž±¸`ÀÌ´Ù. Reduction, Áï ȯ¿øÀº È­ÇÐ ¹ÝÀÀ¿¡¼­ Áß¿äÇÑ °úÁ¤À¸·Î, ÀüÀÚ À̵¿, »êÈ­ »óÅ º¯È­, ±×¸®°í ´Ù¾çÇÑ È­ÇÕ¹°ÀÇ Çü¼ºÀ» Æ÷ÇÔÇÑ´Ù. ÀÌ·¯ÇÑ ¹ÝÀÀÀº À¯±â È­ÇлӸ¸ ¾Æ´Ï¶ó ¹«±â È­ÇÐ, »ýÈ­ÇÐ µî ´Ù¾çÇÑ ºÐ¾ß¿¡¼­¡¦
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Reduction of m-nitroacetophenone(¿¹ºñº¸°í¼­)

Reduction of m-nitroacetophenone(¿¹ºñº¸°í¼­)

Reduction of m-nitroacetophenone(¿¹ºñº¸°í¼­) / 1. ½ÇÇèÁ¦¸ñ 2. ½ÇÇè¸ñÇ¥ 3. ½ÇÇèÀÌ·Ð 4. ½Ã¾à ¹× ÃÊÀÚ 5. ½ÇÇè¹æ¹ý 6. Âü°í¹®Çå / 1. ½ÇÇèÁ¦¸ñ ½ÇÇè Á¦¸ñÀº `m-´ÏÆ®·Î¾Æ¼¼ÅäÆä³íÀÇ È¯¿ø`À¸·Î ¼³Á¤ÇÏ¿´´Ù. º» ½ÇÇèÀÇ ¸ñÀûÀº m-´ÏÆ®·Î¾Æ¼¼ÅäÆä³íÀ» ȯ¿øÇÏ¿© À̸¦ ÅëÇØ »ê¹°ÀÎ m-¾Æ¹Ì³ë¾Æ¼¼ÅäÆä³íÀ» ÇÕ¼ºÇÏ´Â °ÍÀÌ´Ù. m-´ÏÆ®·Î¾Æ¼¼ÅäÆä³íÀº ¹æÇâÁ· È­ÇÕ¹°·Î¼­, À̸¦ ÅëÇÑ È¯¿ø ¹Ý¡¦
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Reduction of m-nitroacetophenone

Reduction of m-nitroacetophenone

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Reduction °á°úº¸°í¼­

Reduction °á°úº¸°í¼­

Reduction °á°úº¸°í¼­ / 1. ½ÇÇèÁ¦¸ñ 2. ½ÇÇè¸ñÀû 3. ½ÇÇè¹æ¹ý 4. ½ÇÇè°á°ú 5. °íÂû 6. Âü°í¹®Çå / 1. ½ÇÇèÁ¦¸ñ ½ÇÇè Á¦¸ñÀº `»êȭȯ¿ø ¹ÝÀÀÀ» ÀÌ¿ëÇÑ ±Ý¼Ó ÀÌ¿ÂÀÇ È¯¿ø`ÀÌ´Ù. ÀÌ ½ÇÇèÀº È­ÇÐ ºÐ¾ß¿¡¼­ Áß¿äÇÑ »êȭȯ¿ø ¹ÝÀÀÀÇ ¿ø¸®¸¦ ÀÌÇØÇÏ°í, À̸¦ ÅëÇØ ±Ý¼Ó ÀÌ¿ÂÀ» ƯÁ¤ Á¶°Ç¿¡¼­ ȯ¿øÇÏ¿© ±Ý¼ÓÀ» ¾ò´Â °úÁ¤À» °üÂûÇÏ´Â µ¥ ¸ñÀûÀÌ ÀÖ´Ù. »êȭȯ¿ø ¹ÝÀÀÀº ÀüÀÚÀÇ À̵¿À» ¼ö¹Ý¡¦
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Reduction of m-nitroacetophenone(°á°úº¸°í¼­)

Reduction of m-nitroacetophenone(°á°úº¸°í¼­)

Reduction of m-nitroacetophenone(°á°úº¸°í¼­) / 1. ½ÇÇè°á°ú 2. Áú¹® 3. ÅäÀÇ 4. Âü°í¹®Çå / 1. ½ÇÇè°á°ú m-nitroacetophenoneÀÇ È¯¿ø ½ÇÇèÀº ÀÌ È­ÇÕ¹°ÀÇ Ä«º¸´Ò±â(ketone group)¸¦ ¾ËÄڿñâ·Î º¯È­½ÃÅ°´Â °úÁ¤À» Æ÷ÇÔÇÑ´Ù. ½ÇÇèÀº ȯ¿øÁ¦ÀÎ ¸®Æ¬ ¾Ë·ç¹Ì´½ ÇÏÀ̵å¶óÀ̵å(LiAlH¸¦ »ç¿ëÇÏ¿© ÁøÇàµÇ¾úÀ¸¸ç, ÀÌ °úÁ¤¿¡¼­ m-nitroacetophenoneÀº Çì¹Ì¾Æ¼¼Å»ÀÇ Áß°£ »ý¼º¹°À» Çü¼ºÇÑ ¡¦
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À¯±âÈ­ÇнÇÇè Reduction

À¯±âÈ­ÇнÇÇè Reduction

À¯±âÈ­ÇнÇÇè Reduction / 1. subject 2. date 3. name 4. principle and object 5. material(apparatus, instruments, reagents) 6. procedure and observation 7. result 8. reference / 1. subject ReductionÀº À¯±âÈ­Çп¡¼­ Áß¿äÇÑ ¹ÝÀÀ À¯ÇüÀÌ´Ù. ÀÌ °úÁ¤Àº ÀϹÝÀûÀ¸·Î È­ÇÕ¹°ÀÇ »ê¼Ò ÇÔ·®À» °¨¼Ò½ÃÅ°°Å³ª ¼ö¼Ò ÇÔ·®À» Áõ°¡½ÃÅ°´Â °ÍÀ» Æ÷ÇÔÇØ ÀüÀÚ¸¦ Ãß°¡ÇÏ´Â ¹ÝÀÀÀ¸·Î ¡¦
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À¯±âÈ­ÇнÇÇè Reduction of aldehyde

À¯±âÈ­ÇнÇÇè Reduction of aldehyde

À¯±âÈ­ÇнÇÇè Reduction of aldehyde / 1. Title 2. Date 3. Purpose 4. Reagent & Apparatus 5. Theory 6. Method 7. Observation 8. Result 9. Discussion 10. Reference / 1. Title À¯±âÈ­ÇнÇÇè¿¡¼­´Â ¸¹Àº ¹ÝÀÀ ¸ÞÄ¿´ÏÁò°ú È­ÇÕ¹° º¯È¯ °úÁ¤À» ¹è¿ì°Ô µÈ´Ù. ƯÈ÷ ¾Ëµ¥ÇÏÀ̵带 ȯ¿øÇÏ´Â ¹ÝÀÀÀº À¯±âÈ­ÇÐÀÇ ±âÃÊÀûÀÎ °³³äÀ» ÀÌÇØÇÏ´Â µ¥ Áß¿äÇÑ ¿ªÇÒÀ» ÇÑ´Ù. ¾Ëµ¥ÇÏÀ̵塦
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¼­¿ï¿©ÀÚ´ëÇб³ À¯±âÈ­ÇнÇÇè Reduction °á°ú ·¹Æ÷Æ®

¼­¿ï¿©ÀÚ´ëÇб³ À¯±âÈ­ÇнÇÇè Reduction °á°ú ·¹Æ÷Æ®

¼­¿ï¿©ÀÚ´ëÇб³ À¯±âÈ­ÇнÇÇè Reduction °á°ú ·¹Æ÷Æ® / 1. Subject 2. Date 3. Name 4-1. Principle 4-2. Object 5. Material (in English) 6. Procedure & Observation 7. Result 8. Discussion 9. Reference / 1. Subject À¯±âÈ­ÇнÇÇè¿¡¼­ ¼öÇàÇÑ Reduction ¹ÝÀÀÀº À¯±â È­ÇÕ¹°ÀÇ ±¸Á¶Àû º¯È­¸¦ ÅëÇØ »êÈ­ »óŸ¦ ³·Ãß´Â Áß¿äÇÑ °úÁ¤ÀÌ´Ù. ReductionÀº ÀϹÝÀûÀ¸·Î¡¦
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[À¯±âÈ­ÇнÇÇèA] reduction with nabh4 ¿¹ºñº¸°í¼­

[À¯±âÈ­ÇнÇÇèA] reduction with nabh4 ¿¹ºñº¸°í¼­

[À¯±âÈ­ÇнÇÇèA] reduction with nabh4 ¿¹ºñº¸°í¼­ / 1. ½ÇÇèÁ¦¸ñ 2. ½ÇÇèÀÏÀÚ 3. ½ÇÇè¿ø¸® ¹× ½Ã¾àÁ¶»ç 4. Âü°í¹®Çå / 1. ½ÇÇèÁ¦¸ñ À¯±âÈ­ÇнÇÇèA¿¡¼­ ÁøÇàÇÏ´Â ¡®È¯¿ø ¹ÝÀÀÀ» ÅëÇÑ ³ªÆ®·ý º¸·¹ÀÌÆ®(NaBH È°¿ë¡¯Àº À¯±âÈ­ÇÕ¹°ÀÇ È¯¿øÈ­ÇÐÀ» ÀÌÇØÇÏ°í ´Ù¾çÇÑ È­ÇÐ ¹ÝÀÀÀÇ ¸ÞÄ¿´ÏÁòÀ» Ž±¸Çϱâ À§ÇÑ Áß¿äÇÑ ½ÇÇèÀÌ´Ù. ³ªÆ®·ý º¸·¹ÀÌÆ®´Â °­·ÂÇÑ È¯¿øÁ¦À̸ç, ÁÖ·Î ¾Ëµ¥ÇÏÀ̵å, ÄÉÅæ,¡¦
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