cyclohexane °Ë»ö°á°ú
100 °Ç (1/10 ÂÊ)
»ó¼¼Á¶°Ç 
 
ÆÄÀÏÁ¾·ù 
|
Synthesis of cyclohexane ¿¹ºñ·¹Æ÷Æ® / 1. Title 2. Date 3. Purpose 4. Reagets & Apparatus 5. Theory 6. Procedure / 1. Title CyclohexaneÀÇ ÇÕ¼ºÀº À¯±âÈÇÐ ºÐ¾ß¿¡¼ Áß¿äÇÑ °ü½É»ç Áß ÇϳªÀÌ´Ù. ÀÌ ¹°ÁúÀº »ê¾÷ÀûÀ¸·Î ³Î¸® »ç¿ëµÇ¸ç, ÁÖ·Î ¼®À¯ÈÇÐ °øÁ¤¿¡¼ µð¿¡Æ¿·»°ú °°Àº ¾ËÄËÀÇ ¼ö¼ÒÈ ¹ÝÀÀÀ» ÅëÇØ Á¦Á¶µÈ´Ù. CyclohexaneÀº ±âº»ÀûÀ¸·Î ¼ø¼öÇÑ µ¿±×¶õ °í¸® ±¸Á¶¸¦ ¡¦ |
|
|
|
|
|
°è»êÈÇÐ ½Ç½À º¸°í¼, Avogadro ÇÁ·Î±×·¥À» ÀÌ¿ëÇÑ Cyclohexane Modeling ¹× ÃÖÀûÈ / 1. ½ÇÇè¸ñÀû 2. ½ÇÇèÀÌ·Ð ¹× ½ÇÇè¹æ¹ý 3. ½ÇÇè°á°ú 4. °á·Ð / 1. ½ÇÇè¸ñÀû ½ÇÇèÀÇ ¸ñÀûÀº Avogadro ÇÁ·Î±×·¥À» ÀÌ¿ëÇÏ¿© »çÀÌŬ·ÎÇí¼¼ÀÎ(Cyclohexane)ÀÇ ºÐÀÚ ±¸Á¶¸¦ ¸ðµ¨¸µÇÏ°í ÃÖÀûÈÇÏ´Â °ÍÀÌ´Ù. »çÀÌŬ·ÎÇí¼¼ÀÎÀº Áß¿äÇÑ À¯±â ÈÇÕ¹°·Î, ÁÖ·Î ÈÇÐ »ê¾÷¿¡¼ ¿ë¸Å³ª ÇÕ¼º Áß°£Ã¼·Î ³Î¸® »ç¡¦ |
|
|
|
|
|
À¯±âÇÕ¼º½ÇÇè 1. Oxidation of Cyclohexane to Hexandedioic Acid / 1. Oxidation of Cyclohexane to Hexandedioic Acid ¸ñÂ÷ ¥°. ½ÇÇè¸ñÀû ¥±. ½ÇÇèÀÌ·Ð / 1. Oxidation 2. ¾ËÄÚ¿ÃÀÇ »êȹÝÀÀ 3. ¾ËÄÚ¿ÃÀÇ »êÈÁ¦ 4. KetoneÀÇ »êÈ 5. Mechanism ¥². ½ÇÇè¹æ¹ý ¥³. ½Ã¾àÁ¶»ç ¥´. Âü°í¹®Çå ¥°. ½ÇÇè¸ñÀû CyclohexaneÀÇ »êÈ´Â À¯±â ÇÕ¼º¿¡¼ Áß¿äÇÑÀÀ Áß Çϳª·Î, ´Ù¾ç¡¦ |
|
|
|
|
|
À¯±âÇÕ¼º½ÇÇè 1. Oxidation of Cyclohexane to Hexanedioic Acid(Adipic Acid) °á°úº¸°í¼ / 1. ½ÇÇè¸ñÀû 2. ½ÇÇè¹æ¹ý 3. ½ÇÇè°á°ú ¹× ºÐ¼® 4. °íÂû / 1. ½ÇÇè¸ñÀû À¯±âÇÕ¼º½ÇÇèÀÇ Ã¹ ¹ø° ÁÖÁ¦ÀÎ »çÀÌŬ·ÎÇí¼¾ÀÇ »êÈ ¹ÝÀÀÀ» ÅëÇØ Çí»êµð¿Â »ê, Áï ¾ÆµðÇÈ»êÀ» ÇÕ¼ºÇÏ´Â ¸ñÀûÀº À¯±âÈÇÕ¹°ÀÇ »êÈ ¹ÝÀÀ¿¡ ´ëÇÑ ÀÌÇظ¦ ÁõÁøÇÏ°í, ½ÇÁ¦ ½ÇÇèÀ» ÅëÇØ ÀÌ·¯ÇÑ ¹ÝÀÀÀ» Á¶ÀÛÇÏ°í °üÂûÇϴ¡¦ |
|
|
|
|
|
1. ½ÇÇèÁ¦¸ñ ½ÇÇè Á¦¸ñÀº `»çÀÌŬ·ÎÇí¼¼ÀÎÀÇ ºê·Î¸ðÇÏÀ̵帰 Çü¼º`ÀÌ´Ù. ÀÌ ½ÇÇèÀº »çÀÌŬ·ÎÇí¼¼Àο¡ ºê·Î¹Î°ú ¹°À» ¹ÝÀÀ½ÃÄÑ ºê·Î¸ðÇÏÀ̵帰À» ÇÕ¼º.. / 1. ½ÇÇèÁ¦¸ñ 2. ½ÇÇè°á°ú 3. ÅäÀÇ 4. Âü°í¹®Çå / 1. ½ÇÇèÁ¦¸ñ ½ÇÇè Á¦¸ñÀº `»çÀÌŬ·ÎÇí¼¼ÀÎÀÇ ºê·Î¸ðÇÏÀ̵帰 Çü¼º`ÀÌ´Ù. ÀÌ ½ÇÇèÀº »çÀÌŬ·ÎÇí¼¼Àο¡ ºê·Î¹Î°ú ¹°À» ¹ÝÀÀ½ÃÄÑ ºê·Î¸ðÇÏÀ̵帰À» ÇÕ¼ºÇÏ´Â °úÁ¤À¸·Î, ½ºÅ×·¹¿À¡¦ |
|
|
|
|
|
1.½ÇÇèÁ¦¸ñ ½ÃŬ·ÎÇí»êÀÇ ÀÔü¼±ÅÃÀûÀÎ ÇÕ¼º`ÀÌ´Ù. ÀÌ ½ÇÇèÀº ½ÃŬ·ÎÇí»êÀ» Ãâ¹ß¹°Áú·Î »ç¿ëÇÏ¿© ºê·Î¸ðÇÏÀ̵帰À» ÇÕ¼ºÇÏ´Â °úÁ¤À» ´Ù·é´Ù. ºê·Î¸ðÇÏ.. / 1.½ÇÇèÁ¦¸ñ 2.½ÇÇ賯¥ 3.½ÇÇè¸ñÀû 4.½ÇÇèÀÌ·Ð 5.½Ã¾à ¹× ±â±¸ 6.½ÇÇè¹æ¹ý 7.Âü°í¹®Çå / 1.½ÇÇèÁ¦¸ñ ½ÃŬ·ÎÇí»êÀÇ ÀÔü¼±ÅÃÀûÀÎ ÇÕ¼º`ÀÌ´Ù. ÀÌ ½ÇÇèÀº ½ÃŬ·ÎÇí»êÀ» Ãâ¹ß¹°Áú·Î »ç¿ëÇÏ¿© ºê·Î¸ðÇÏÀ̵帰À» ÇÕ¼ºÇÏ´Â °úÁ¤¡¦ |
|
|
|
|
|
[À¯±âÈÇнÇÇè1] ½ÇÇè7 ¿¹ºñ·¹Æ÷Æ® stereospecific Preparation 1. Bromohydrin formation of cyclohexane / 1.½ÇÇèÁ¦¸ñ 2.½ÇÇ賯¥ 3.½ÇÇè¸ñÀû 4.½ÇÇèÀÌ·Ð 5.½Ã¾à ¹× ±â±¸ 6.½ÇÇè¹æ¹ý 7.Âü°í¹®Çå / 1.½ÇÇèÁ¦¸ñ ½ÇÇè Á¦¸ñÀº `ºê·Î¸ðÇÏÀ̵帰 Çü¼º ¹ÝÀÀÀ» ÅëÇÑ »çÀÌŬ·ÎÇí¼¼ÀÎÀÇ ÀÔüƯÀÌÀû ÇÕ¼º`ÀÌ´Ù. ÀÌ ½ÇÇèÀº Ưº°È÷ »çÀÌŬ·ÎÇí¼¼Àΰú ºê·Î¹Î, ±×¸®°í ¼ö»êȹ°ÀÌ ¹ÝÀÀÇÏ¿© ºê¡¦ |
|
|
|
|
|
[À¯±âÈÇнÇÇè1] ½ÇÇè7 °á°ú·¹Æ÷Æ® stereospecific Preparation 1. Bromohydrin formation of cyclohexane / 1. ½ÇÇèÁ¦¸ñ 2. ½ÇÇè°á°ú 3. ÅäÀÇ 4. Âü°í¹®Çå / 1. ½ÇÇèÁ¦¸ñ ½ÇÇè Á¦¸ñÀº ¡®Bromohydrin formation of cyclohexane¡¯ÀÌ´Ù. ÀÌ ½ÇÇèÀº »çÀÌŬ·ÎÇí»êÀÇ ºê·Î¸ðÇÏÀ̵帰 ÈÇÕ¹°ÀÇ Á¤ stereospecific ÇÕ¼ºÀ» ´Ù·ç°í ÀÖ´Ù. ºê·Î¸ðÇÏÀ̵帰Àº ÇÒ·ÎÁ¨°ú ÇÏÀ̵å·Ï½Ç ±â°¡ µ¿½Ã¿¡¡¦ |
|
|
|
|