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 Synthesis of Acetanilide from aniline ȍ˟

Synthesis of Acetanilide from aniline ȍ˟

Synthesis of Acetanilide from aniline »çÀü / ½ÇÇè ¸ñÀû ¾Æ´Ò¸°ÀÇ (ÇÁ·¹µ¨-Å©·¡ÇÁÃ÷ ¾Æ½ÇÈ­ )¹ÝÀÀÀ» ÀÌ¿ëÇÏ¿© ¿©·¯°¡Áö À¯¿ëÇÑ È­ÇÕ¹°ÇÕ¼ºÀÇ Áß°£Ã¼·Î »ç¿ëµÇ´Â(¾Æ¼¼Æ® ¾Æ´Ò¶óÀ̵å )ÇÕ¼º¹ýÀ» ¹ÝÀÀÀåÄ¡¼³°è, ¹ÝÀÀ ¸ÞÄ¿´ÏÁò ¹× ºÐ¸®Á¤Á¦°øÁ¤À» ÀÌÇØÇÏ°í ½ÇÇèÀ» ÅëÇØ Á¦Á¶Çغ»´Ù. ½ÇÇè ¹æ¹ý 500ml Round Flask¿¡ Aniline 1 molÀ» ³Ö°í Acetic acid 1.1 molÀ» õõÈ÷ °¡ÇÑ´Ù. ¿Âµµ¸¦ º¸¸ç¡¦
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 Ferrocene derivate synthesis

Ferrocene derivate synthesis

Ferrocene derivate synthesis / CONTENTS 1. ½ÇÇèÁ¦¸ñ 2. ½ÇÇè¸ñÀû 3. ½ÇÇ賯¥ 4. ½ÇÇèÀÌ·Ð 5. ½ÇÇè¹æ¹ý 6. ±â±¸ ¹× ½Ã¾à 7. Âü°í¹®Çå R REPORT Forrocene Derivate Synthesis °ú¸ñ¸í Áöµµ±³¼ö Çаú Çйø À̸§ Á¦ÃâÀÏ 1. ½ÇÇèÁ¦¸ñ: Ferrocene derivate synthesis 2. ½ÇÇè¸ñÀû: MetalloceneÀÇ ÇϳªÀÎ FerroceneÀ» ÇÕ¼ºÇÏ°í, TLC¸¦ ÅëÇØ Ferrocene derivatesÀ»¡¦
Àü±âÀüÀÚ   10page   2,900 ¿ø
 Synthesis of Silica

Synthesis of Silica

Synthesis of Silica / CONTENTS 1. ½ÇÇèÁ¦¸ñ 2. ½ÇÇè¸ñÀû 3. ½ÇÇ賯¥ 4. ½ÇÇèÀÌ·Ð 5. ½ÇÇè¹æ¹ý 6. ±â±¸ ¹× ½Ã¾à 7. Âü°í¹®Çå R REPORT Synthesis of Silica °ú¸ñ¸í Áöµµ±³¼ö Çаú Çйø À̸§ Á¦ÃâÀÏ 1. ½ÇÇèÁ¦¸ñ: Synthesis of silica 2. ½ÇÇè¸ñÀû: Stober synthesis method¸¦ ÀÌ¿ëÇÏ¿© ½ÇÇè Á¶°Çµé¿¡ º¯È­¸¦ ÁÖ¾î ¿©·¯ °¡Áö Å©±âÀÇ silica particleÀ» ¸¸µé¾î¡¦
Àç·á   7page   1,900 ¿ø
[È­ÇнÇÇè ·¹Æ÷Æ® º¸°í¼­] PC (Synthesis of Polycarbonate) manual

[È­ÇнÇÇè ·¹Æ÷Æ® º¸°í¼­] PC (Synthesis of Polycarbonate) manual

[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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Synthesis and characterization of Tertronic-PCL copolymer

Synthesis and characterization of Tertronic-PCL copolymer

¡¥ [¹°ÁúºÐ¼®½ÇÇè ¼³°è º¸°í¼­] Synthesis and characterization of Tertronic-PCL copolymer »ý¸íºÐÀÚ°øÇкΠÀÀ¿ëÈ­Çаú 200421887 ÇãÁöÈ£ ½ÇÇèÁ¦¸ñ Synthesis and characterization ofTertronic-PCL copolymer ½ÇÇè¸ñÀû FT-IR, ©öH-NMR, Fluorescent¸¦ ÀÌ¿ëÇÏ¿© ÇÕ¼º¹°ÁúÀÎ Tetronic-PCLÀ» ºÐ¼®Çغ»´Ù. ½ÇÇè°úÁ¤ 1) Tetronic-PCL ÇÕ¼º ¿ì¼± ¼ø¼öÇÑ TetronicÀ» ¾ò±â¡¦
±âŸ½ÇÇè   7page   1,500 ¿ø
¹ÙÀÌ¿À³ª³ëÇкΠ³ª³ë °øÇнÇÇè ·¹Æ÷Æ® Synthesis of silica nanoparticles

¹ÙÀÌ¿À³ª³ëÇкΠ³ª³ë °øÇнÇÇè ·¹Æ÷Æ® Synthesis of silica nanoparticles

¹ÙÀÌ¿À³ª³ëÇкΠ³ª³ë °øÇнÇÇè ·¹Æ÷Æ® Synthesis of silica nanoparticles / ³ª³ë °øÇнÇÇè ·¹Æ÷Æ® Synthesis of silica nanoparticles ¹ÙÀÌ¿À³ª³ëÇкΠ1. Introduction -Silica nano particle ÀÇ °úÇÐÀûÀÎ ¿¬±¸¿¡¼­ÀÇ È°¿ëÀº ´Ù¾çÇÏ´Ù. È¿¼Ò, ¾àÇÐ, ÀüÀÚ±âÇÐ, ¹ÙÀÌ¿À ¼¾¼­, ¹ÝµµÃ¼ µîÀÇ ´Ù¾çÇÑ ºÎ¹®¿¡¼­ È°¿ëÀ» ÇÒ ¼ö ÀÖ´Ù. »ê¾÷ÀûÀÎ Ãø¸é¿¡¼­ Á¢±ÙÇßÀ» ¶§, ÀÌ nano pa¡¦
°øÇбâ¼ú   7page   1,000 ¿ø
[ÀÚ¿¬°úÇÐ] ¹«±âÈ­ÇнÇÇè - The Synthesis of [M(acac)3] (M ¡ë Cr, Fe, and Co)

[ÀÚ¿¬°úÇÐ] ¹«±âÈ­ÇнÇÇè - The Synthesis of [M(acac)3] (M ¡ë Cr, Fe, and Co)

[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¡¦
¹°¸®È­ÇÐ   15page   2,000 ¿ø
[ÀÚ¿¬°úÇÐ] À¯±âÈ­ÇнÇÇè - Synthesis of Acetanilide

[ÀÚ¿¬°úÇÐ] À¯±âÈ­ÇнÇÇè - Synthesis of Acetanilide

[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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[È­ÇнÇÇè ·¹Æ÷Æ® º¸°í¼­] Æú¸®Ä«º¸³×ÀÌÆ® °á°ú

[È­ÇнÇÇè ·¹Æ÷Æ® º¸°í¼­] Æú¸®Ä«º¸³×ÀÌÆ® °á°ú

[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¡¦
¹°¸®È­ÇÐ   5page   1,000 ¿ø
½ÇÇ躸°í¼­- À¯±âÈ­ÇÐ ½ÇÇè[TLC]

½ÇÇ躸°í¼­- À¯±âÈ­ÇÐ ½ÇÇè[TLC]

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¡¦
¹°¸®È­ÇÐ   3page   1,200 ¿ø




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