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[ÈÇнÇÇè ·¹Æ÷Æ® º¸°í¼] PC (Synthesis of Polycarbonate) manual / Title : Synthesis of Polycarbonate. - BPA, DPC¸¦ ¹ÝÀÀ½ÃÄѼ Polycarbonate¸¦ ÇÕ¼ºÇÑ´Ù. 1. Scheme. 1). BPA formula : (CH3)2C(C6H4OH)2 M.W : 228.29 scheme : 2). DPC formula : (C6H5O)2CO M.W : 214.22 scheme : 3). reaction. A : BPA. B : DPC. C : polycarbonate. P : phenol. 2. Rea¡¦
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[ÀÚ¿¬°úÇÐ] ¹«±âÈÇнÇÇè - The Synthesis of [M(acac)3] (M ¡ë Cr, Fe, and Co) / ¹«±âÈÇнÇÇè - The Synthesis of [M(acac)3] (M ¡ë Cr, Fe, and Co) ¸ñÂ÷ I. Introduction. 3 ~ 4 II. Results ¼öµæ·ü . 4 ~ 5 Àç°áÁ¤ .5 IR spectrum6 ~ 9 III. Experimental Section .. 10~11 IV. Table (»ç¿ëÇÑ ½Ã¾à) 11 V. Questions Synthesis 11~13 Recrystallization . 13~15 VI. Discus¡¦
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2,000 ¿ø
[ÀÚ¿¬°úÇÐ] À¯±âÈÇнÇÇè - Synthesis of Acetanilide / À¯±âÈÇнÇÇè - Synthesis of Acetanilide °¡. ½ÇÇè¸ñÀû ¾Æ´Ò¸°(Aniline)¿¡ ¹«¼öÃÊ»ê(Acetic anhyride)°ú ºùÃÊ»ê(Acetic acid)ÀÇ È¥ÇÕ¾×À» ÷°¡ÇÏ°í °¡¿ÇÏ¸é ¾Æ´Ò¸°ÀÇ ¾Æ¹Î±â¿¡ ¾Æ¼¼Æ¿±â(-COCH3)°¡ µµÀÔµÇ¾î ¾Æ¼¼Æ®¾Æ´Ò¶óÀ̵尡 »ý¼ºµÈ´Ù. ÀÌ ¹ÝÀÀÀ» ¾Æ¼¼Æ¿È ¹ÝÀÀ(Acetylation)À̶ó ÇÑ´Ù. 1Â÷¿Í 2Â÷ ¼ö¼Ò ¾Æ¹ÎÀº È°¼º¼ö¼Ò¿øÀÚ¸¦¡¦
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2,000 ¿ø
[ÈÇнÇÇè ·¹Æ÷Æ® º¸°í¼] Æú¸®Ä«º¸³×ÀÌÆ® °á°ú / 1. ½ÇÇè Á¦¸ñ Synthesis of Polycarbonate 2. ½ÇÇè ¸ñÀû BPA ¿Í DPCÀÇ ¹ÝÀÀÀ» ÅëÇØ Æú¸®Ä«º¸³×ÀÌÆ®¸¦ ÇÕ¼ºÇÏ°í À¯º§·Îµå Á¡µµ°è¸¦ ÀÌ¿ëÇÏ¿© Á¡µµ Æò±Õ ºÐÀÚ·®À» ±¸Çغ»´Ù. 3. ½ÇÇè ÀÌ·Ð 1) Reaction A +BC + D A : BPAB : DPCC : Polycarbonate D : Phenol 2) BPA (Bisphenol-A) -ºÐÀÚ½Ä : (CH3)2C(C6H4OH)2 -ºÐÀÚ·® : 228.29 -¼ºÁú¡¦
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1,000 ¿ø
½ÇÇ躸°í¼- À¯±âÈÇÐ ½ÇÇè[TLC] / REPORT OF LABORATORY EXPERIMENTS IN ORGANIC CHEMISTRY ¨ç 1. Subject : Thin Layer Chromatography (TLC) 2. Date : 3. Name : - 4. Principle : Non-volatile reaction mixtureÀÇ qualitative examination¿¡ »ç¿ëÀÌ µÇ´Â simpleÇÏ°í rapidÇÑ ÀÏÁ¾ÀÇ liquid chromatograghy·Î glass, aluminum ¶Ç´Â plastic plate¿¡ solid stationary phase°¡ coa¡¦
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[ÀÚ¿¬°úÇÐ]À¯±âÈÇнÇÇè - E2¹ÝÀÀÀ¸·Î cyclohexeneÀ» ÇÕ¼º / 1. TITLE : Synthesis of cyclohexene from cyclohexanol 2. DATE : 3. OBJECT : E2¹ÝÀÀÀ¸·Î cyclohexeneÀ» ÇÕ¼ºÇÒ ¼ö ÀÖ´Ù. 4. THEORY & PRINCIPLES #. ¾ËÄÚ¿ÃÀÇ Å»¼ö (Dehydration of Alcohols) »êÀÌ Ã˸ÅÀÛ¿ëÀ» ÇÏ´Â ¾ËÄÚ¿ÃÀÇ Å»¼ö´Â mechanism »óÀ¸·Î º¼ ¶§ E1 eliminationÀ¸·Î ºÐ·ù ÇÒ ¼ö ÀÖ´Ù. ÀÌ ¹ÝÀÀÀº hydroxyl oxy¡¦
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[ÀÚ¿¬°úÇÐ]À¯±âÈÇнÇÇè - E2¹ÝÀÀÀ¸·Î cyclohexeneÀ» ÇÕ¼º / 1. TITLE : Synthesis of cyclohexene from cyclohexanol 2. DATE : 3. OBJECT : E2¹ÝÀÀÀ¸·Î cyclohexeneÀ» ÇÕ¼ºÇÒ ¼ö ÀÖ´Ù. 4. THEORY & PRINCIPLES #. ¾ËÄÚ¿ÃÀÇ Å»¼ö (Dehydration of Alcohols) »êÀÌ Ã˸ÅÀÛ¿ëÀ» ÇÏ´Â ¾ËÄÚ¿ÃÀÇ Å»¼ö´Â mechanism »óÀ¸·Î º¼ ¶§ E1 eliminationÀ¸·Î ºÐ·ù ÇÒ ¼ö ÀÖ´Ù. ÀÌ ¹ÝÀÀÀº hydroxyl oxy¡¦
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[ÀÚ¿¬°úÇÐ] [À¯±âÈÇнÇÇè] 1-HexeneÀ» starting material·Î ÇÏ¿© hydroboration °ú oxidation ¹ÝÀÀÀ» ¿¬¼ÓÀûÀ¸·Î ÁøÇà ÇÏ¿© ÃÖÁ¾ÀûÀ¸·Î 1-He / 1.Introduction À̹ø ½ÇÇèÀº 1-HexeneÀ» starting material·Î ÇÏ¿© hydroboration °ú oxidation ¹ÝÀÀÀ» ¿¬¼ÓÀûÀ¸·Î ÁøÇà ÇÏ¿© ÃÖÁ¾ÀûÀ¸·Î 1-HexanolÀ» ÇÕ¼ºÇÏ´Â ½ÇÇèÀÌ´Ù. ù ¹ø° ¹ÝÀÀÀÎ hydronorationÀº borane (BH3)ÀÌ THF solvent¿¡¼ 1-¡¦
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1,200 ¿ø