Compound °Ë»ö°á°ú

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[A+] º¹ÇտɼÇ(COMPOUND OPTION) ¹×µî°¡°Ýº¹ÇտɼÇ(AT THE MONEY COMPOUND OPTION)ÀDZ¸Á¶¿Í °¡Ä¡¿¡ °üÇÑ ¼Ò°í

[A+] º¹ÇտɼÇ(COMPOUND OPTION) ¹×µî°¡°Ýº¹ÇտɼÇ(AT THE MONEY COMPOUND OPTION)ÀDZ¸Á¶¿Í °¡Ä¡¿¡ °üÇÑ ¼Ò°í

. ¼­ ·Ð . º¸ÇտɼÇÀÇ ±¸Á¶¿Í °¡Ä¡ ¹× ¹Î°¨µµºÐ¼® . º¯Çüº¹ÇտɼÇÀÇ ±¸Á¶¿Í °¡Ä¡ºÐ¼® . °á ·Ð º¹Çտɼǹ׵°Ýº¹ÇտɼÇÀDZ¸Á¶¿Í°¡Ä¡¿¡°üÇѼҰí / ¥±.º¹ÇտɼÇÀÇ ±¸Á¶¿Í °¡Ä¡¹× ¹Î°¨µµºÐ¼® 1. º¹ÇտɼÇÀÇ ±¸Á¶ À§¿¡¼­ º»´ë·Î º¹ÇտɼÇÀº ¿É¼Ç¿¡ ´ëÇÑ ¿É¼Ç, Áï ±× ±¸Á¶°¡ ÁÖ¾îÁø ¿É¼Ç(Çà»ç´ë»ó¿É¼Ç)À» ¹Ì·¡ÀÇ ÀÏÁ¤ÇÑ ½ÃÁ¡¿¡ ¹Ì¸® Á¤ÇÑ °¡°ÝÀ¸·Î ¸Å¼öÇϰųª(ÄݿɼÇ) ¸ÅµµÇÒ(Dz¿É¡¦
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Èֹ߼º À¯±âÈ­ÇÕ¹°. (Volatile Organic Compounds,VOC)

Èֹ߼º À¯±âÈ­ÇÕ¹°. (Volatile Organic Compounds,VOC)

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 ¸í¸í¹ý (Nomenclature of Organic Compounds)

À¯±âÈ­ÇÕ¹°ÀÇ ¸í¸í¹ý (Nomenclature of Organic Compounds)

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

À¯±â ÀÛ¿ë±â(Functional Graoup Idevfication of Organic Compounds by the Use of Chemical Reaction) ¿¹ºñ

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

À¯±âÀÛ¿ë±â(Functional Graoup Idevfication of Organic Compounds by the Use of Chemical Reaction) °á°ú

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¡¦
·¹Æ÷Æ® > °øÇбâ¼ú   2page   3,000 ¿ø
Chemical compound extraction

Chemical compound extraction

Chemical compound extraction / 1. ÃßÃâ 1) Ãþ ºÐ¸® 2) rotary evaporator 2. °íÂû / 1. ÃßÃâ ÃßÃâÀº È­ÇÐ ¹°ÁúÀ» ÀÚ¿¬ »óÅ¿¡¼­ ºÐ¸®ÇÏ´Â °úÁ¤À¸·Î, ¿©·¯ °¡Áö ¹æ¹ý°ú ±â¹ýÀ» È°¿ëÇÏ¿© ¿øÇÏ´Â È­ÇÕ¹°À» È¿°úÀûÀ¸·Î ¾ò´Â ±â¼úÀÌ´Ù. ÀÌ °úÁ¤Àº ½Ä¹°, ¹Ì»ý¹°, µ¿¹° ¹× ±âŸ ÀÚ¿¬¿¡¼­ ¹ß»ýÇÏ´Â º¹ÇÕ È¥ÇÕ¹°¿¡¼­ ƯÁ¤ ¼ººÐÀ» ºÐ¸®Çϱâ À§ÇØ ÁÖ·Î »ç¿ëµÈ´Ù. ÃßÃâÀÇ ¸ñÀûÀº ºÐ¼®, ¿¬±¸, ¡¦
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Aromatic Compounds

Aromatic Compounds

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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Organic Compound Decomposition Using TiO2 Photocatalyst °á°úº¸°í¼­

Organic Compound Decomposition Using TiO2 Photocatalyst °á°úº¸°í¼­

1. ½ÇÇè ³¯Â¥ ½ÇÇè ³¯Â¥´Â 2023³â 10¿ù 5ÀÏÀÌ´Ù. À̳¯ÀÇ ½ÇÇèÀº ÇÞ»ìÀÌ Àß µå´Â ¿ÀÈÄ ½Ã°£´ë¿¡ ÁøÇàµÇ¾úÀ¸¸ç, ±â¿ÂÀº ¾à 22µµ, ½Àµµ´Â.. / 1. ½ÇÇè ³¯Â¥ 2. °³¿ä 3. Results (1) MB 2ºÐ¸¶´Ù ÃøÁ¤ (2) TiO2 Photocatalyst + MB 10Ãʸ¶´Ù ÃøÁ¤ / 1. ½ÇÇè ³¯Â¥ ½ÇÇè ³¯Â¥´Â 2023³â 10¿ù 5ÀÏÀÌ´Ù. À̳¯ÀÇ ½ÇÇèÀº ÇÞ»ìÀÌ Àß µå´Â ¿ÀÈÄ ½Ã°£´ë¿¡ ÁøÇàµÇ¾úÀ¸¸ç, ±â¿ÂÀº ¾à 22µµ, ½Àµµ¡¦
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[A£«·¹Æ÷Æ®][¹«±âÈ­ÇÐ]Separation of Enantiomer from Racemic [Co(en)3]3£«Compound

[A£«·¹Æ÷Æ®][¹«±âÈ­ÇÐ]Separation of Enantiomer from Racemic [Co(en)3]3£«Compound

1. Result Racemic ÄÚ¹ßÆ® º¹ÇÕü [Co(en)3]3+ÀÇ ºÐ¸® °úÁ¤¿¡¼­ ÁÖ¿ä °á°ú´Â ¼º°øÀûÀ¸·Î µÎ °³ÀÇ ¿¡³ª¾ÈƼ¿À¸Ó¸¦ ºÐ¸®ÇÏ°í Á¤.. / 1. Result 2. Further study 3. Reference / 1. Result Racemic ÄÚ¹ßÆ® º¹ÇÕü [Co(en)3]3+ÀÇ ºÐ¸® °úÁ¤¿¡¼­ ÁÖ¿ä °á°ú´Â ¼º°øÀûÀ¸·Î µÎ °³ÀÇ ¿¡³ª¾ÈƼ¿À¸Ó¸¦ ºÐ¸®ÇÏ°í Á¤Á¦ÇÑ °ÍÀÌ´Ù. Ãʱ⠴ܰ迡¼­ racemic [Co(en)3]3+ È­ÇÕ¹°ÀÇ ±¤ÇÐÀû ¼øµµ¸¦ Æò¡¦
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¼­¿ï´ëÇб³ À¯±â¹«±â½ÇÇè - Oxidation of Organic Compounds (2¹ø° ½ÇÇè)

¼­¿ï´ëÇб³ À¯±â¹«±â½ÇÇè - Oxidation of Organic Compounds (2¹ø° ½ÇÇè)

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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