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- 1ÁÖÂ÷ : Structure & Bonding, Alkane, Cycloalkane
- 2ÁÖÂ÷ : Alkene, Alkyne, Stereochemistry
- 3ÁÖÂ÷ : Alkyl Halides, Free Radical
- 4ÁÖÂ÷ : Nucleophilic Substitution & Elimination
- 5ÁÖÂ÷ : Diene, Aromatic Compounds
- 6ÁÖÂ÷ : Alcohol, Ether
- 7ÁÖÂ÷ : Carbonyl Compounds
- 8ÁÖÂ÷ : Amine, Pericyclic Reaction
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1°­ [1-1] ½ÉÈ­À¯±â O.T   43ºÐ
2°­ [1-2] CH.1 Structure / Bonding   100ºÐ
3°­ [1-3] 1.3 °ø¸íÈ¥¼º ÀÌ·Ð   74ºÐ
4°­ [1-4] 1.4 ºÐÀڱ˵µÇÔ¼ö ÀÌ·Ð   83ºÐ
5°­ [2-1] CH.2 Alkanes   103ºÐ
6°­ [2-2] 2.3 ºÐÀÚ°£ Èû°ú ¹°¸®Àû ¼ºÁú   91ºÐ
7°­ [2-3] 2.4 AlkaneÀÇ ÀÚÀ¯¶óµðÄ® ġȯ¹ÝÀÀ   58ºÐ
8°­ [3-1] CH.3 Stereochemistry of Alkanes, Cycloalkanes   80ºÐ
9°­ [3-2] 3.3 CyclohexaneÀÇ ÇüÅ   81ºÐ
10°­ [3-3] 3.6 ÀÌġȯ CyclohexaneÀÇ ÇüÅÂ¿Í Æ÷ÅÙ¼È ¿¡³ÊÁö   75ºÐ
11°­ [4-1] CH.4 Principles of Polar Reaction   59ºÐ
12°­ [4-2] 4.2 »ê¿°±âÀÇ ±âº»ÀÌ·Ð   72ºÐ
13°­ [4-3] 4.4 À¯±â±Ø¼º¹ÝÀÀ°³¿ä   90ºÐ
14°­ [5-1] CH.5 Alkenes, Structure and Reactivity   85ºÐ
15°­ [5-2] 5.3 ¾ËÄËÀÇ ±¸Á¶ - ¾ÈÁ¤µµ »ó°ü°ü°è   90ºÐ
16°­ [5-3] 5.5 Hammond`s °¡¼³   87ºÐ
17°­ [6-1] CH.6 Alkenes, Reactions and Synthesis   93ºÐ
18°­ [6-2] 6.4 Ä£ÀüÀÚ¼º ÷°¡ ¹ÝÀÀ - ÇÒ·ÎÁ¨°ú ¹°ÀÇ Ã·°¡   99ºÐ
19°­ [6-3] 6.8 Ä«º¥ÀÇ Ã·°¡ ¹ÝÀÀ   79ºÐ
20°­ [6-4] 6.12 ¿¬¼â ¼ºÀå ÁßÇÕ ¹ÝÀÀ   46ºÐ
21°­ [7-1] CH.7 Alkenes   81ºÐ
22°­ [7-2] 7.3 Ä£ÀüÀÚ¼º ÇÒ·ÎÁ¨ ÷°¡ ¹ÝÀÀ   86ºÐ
23°­ [7-3] 7.6 »êÈ­ ¹ÝÀÀ   38ºÐ
24°­ [8-1] CH.8 Stereochemistry   90ºÐ
25°­ [8-2] 8.3 Ä«À̶ö ȯ°æ°ú Ä«À̶ö ¼ºÁú - ±¤ÇÐÈ°¼º   93ºÐ
26°­ [8-3] 8.6 ºÎºÐ ÀÔü À̼ºÁúüÀÇ ¹°¸®Àû ¼ºÁú   98ºÐ
27°­ [9-1] CH.9 Alkyl halide   96ºÐ
28°­ [9-2] 9.3 ÀÚÀ¯¶óµðÄ® ¾Ë¸± ġȯ ¹ÝÀÀ   68ºÐ
29°­ [9-3] 9.5 À¯±â±Ý¼Ó È­ÇÕ¹°   57ºÐ
30°­ [10-1] CH.10 Nucleophilc Substitution, Elimination   90ºÐ
31°­ [10-2] 10.4 ´ÜºÐÀÚ¼º Ä£ÇÙ¼º ġȯ¹ÝÀÀ Sɴ1   102ºÐ
32°­ [10-3] 10.6 Á¦°Å¹ÝÀÀ   88ºÐ
33°­ [10-4] 10.7 ¹ÝÀÀÀ¯ÇüÆǴܹý   58ºÐ
34°­ [11-1] CH.11 Conjugated Dienes   79ºÐ
35°­ [11-2] 11.3 Diels-Alder °í¸®È­ ÷°¡ ¹ÝÀÀ   104ºÐ
36°­ [12-1] CH.12 Benzene And Aromaticity   98ºÐ
37°­ [12-2] 12.3 ¹Ý¹æÇâÁ·¼º   101ºÐ
38°­ [13-1] CH.13 Electrophilic Aromatic Substitution   89ºÐ
39°­ [13-2] 13.3 ÀÏġȯ º¥Á¨ÀÇ ¹ÝÀÀ¼Óµµ - È°¼ºÈ­±â¿Í È°¼º °¨¼Ò±â   80ºÐ
40°­ [13-3] 13.5 Ä£ÇÙ¼º ¹æÇâÁ· ġȯ¹ÝÀÀ : ÷°¡-Á¦°Å ¹ÝÀÀ   72ºÐ
41°­ [13-4] 13.7 Á¢ÇÕ°í¸®¿Í ÀÌÁ¾°í¸®ÀÇ ¹ÝÀÀ   104ºÐ
42°­ [13-5] 13.9 º¥Á¨À¯µµÃ¼ÀÇ È¯¿ø   17ºÐ
43°­ [14-1] CH.14 Alcohols, Phenols   93ºÐ
44°­ [14-2] 14.4 ¾ËÄÚ¿ÃÀÇ Á¦¹ý - Ä«º¸´Ò ȯ¿ø ¹ÝÀÀ   76ºÐ
45°­ [14-3] 14.7 ¾ËÄÚ¿ÃÀÇ »ê¼Ò ÀÌÅ»±â - Ä£ÇÙ¼º ġȯ ¹ÝÀÀ   81ºÐ
46°­ [14-4] 14.9 ¾ËÄÚ¿ÃÀÇ »êÈ­¹ÝÀÀ   87ºÐ
47°­ [15-1] CH.15 Ethers And Epoxides   88ºÐ
48°­ [15-2] 15.4 ¿¡Æø»çÀ̵åÀÇ Á¦¹ý   71ºÐ
49°­ [15-3] 15.6 Å©¶ó¿î¿¡ÅÍ   39ºÐ
50°­ [16-1] 16 Aldehyde, Ketones   86ºÐ
51°­ [16-2] 16.5 Å»¼ö¹ÝÀÀÀ» µ¿¹ÝÇÏ´Â ÆòÇü÷°¡¹ÝÀÀ   71ºÐ
52°­ [16-3] 16.8 wittig ¹ÝÀÀ°ú cannizzaro ¹ÝÀÀ   70ºÐ
53°­ [17-1] CH.17 Carboxylic Acids and Nitriles   67ºÐ
54°­ [17-2] 17.3 Ä«º¹½Ç»êÀÇ Á¦¹ý°ú ¹ÝÀÀ   76ºÐ
55°­ [18-1] CH.18 Carboxylic acid derivatives   70ºÐ
56°­ [18-2] 18.3 »ê ¿°È­¹°°ú »ê ¹«¼ö¹°ÀÇ Ä£ÇÙ¼º, ¾Æ½Ç, ġȯ ¹ÝÀÀ   82ºÐ
57°­ [18-3] 18.5 ¾Æ¸¶À̵åÀÇ Ä£ÇÙ¼º, ¾Æ½Ç ġȯ ¹ÝÀÀ   43ºÐ
58°­ [19-1] CH.19 Carbonyl Alpha Reaction   65ºÐ
59°­ [19-2] 19.3 ¿£¿Ã À½À̿ ģÇÙüÀÇ ¾ËÆÄ Ä¡È¯   69ºÐ
60°­ [19-3] 19.5 ¾Ëµ¹ ÃàÇÕ ¹ÝÀÀ   76ºÐ
61°­ [19-4] 19.7 Michael ÷°¡ ¹ÝÀÀ°ú Stork ¿£¾Æ¹Î ÇÕ¼º¹ý   29ºÐ
62°­ [20-1] CH.20 Amines   63ºÐ
63°­ [20-2] 20.3 ¾Æ¹ÎÀÇ Á¦¹ý   67ºÐ
64°­ [20-3] 20.4 ¾Æ¹ÎÀÇ ¹ÝÀÀ   73ºÐ
65°­ [21-1] CH.21 Pericyclic Reaction   86ºÐ
66°­ [21-2] 21.4 ½Ã±×¸¶ °áÇÕ ÀÚ¸®¿Å±è ¹ÝÀÀ ¢ºÁ¾°­   50ºÐ
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