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"https://www.masterorganicchemistry.com/2013/02/13/how-tyrell-got-the-highest-grade-in-her-organic-chemistry-course/", "published_at": "2013-02-13T21:22:44+00:00" }, { "id": "01a0bbd4-9f6e-70ef-8f77-7c980b1bcf38", "title": "Hydrohalogenation of Alkenes and Markovnikov’s Rule", "url": "https://www.masterorganicchemistry.com/2013/02/08/markovnikovs-rule-1/", "published_at": "2013-02-08T15:15:39+00:00" }, { "id": "01a0bc0e-e752-704e-a32e-b28722a58271", "title": "pKa Values Span 60 Orders Of Magnitude", "url": "https://www.masterorganicchemistry.com/2013/01/25/putting-acidity-in-perspective/", "published_at": "2013-01-25T18:49:03+00:00" }, { "id": "01a0bb53-d47c-7111-a867-f975dc1c6436", "title": "Alkene Addition Reactions: Regioselectivity and Stereoselectivity (Syn/Anti)", "url": "https://www.masterorganicchemistry.com/2013/01/22/alkene-addition-regioselectivity-syn-anti/", "published_at": "2013-01-22T19:51:08+00:00" }, { "id": "01a0bbdf-870c-7373-8558-85f4267ac9eb", "title": "Wrapup: The Key Factors For Determining SN1/SN2/E1/E2", "url": "https://www.masterorganicchemistry.com/2013/01/18/wrapup-the-quick-n-dirty-guide-to-sn1sn2e1e2/", "published_at": "2013-01-18T13:32:09+00:00" }, { "id": "01a0bbdf-870c-7373-8558-85f424f57bf8", "title": "How Chris Aced Org 1 and Org 2", "url": "https://www.masterorganicchemistry.com/2013/01/15/how-chris-aced-org-1-and-org-2/", "published_at": "2013-01-15T14:10:25+00:00" }, { "id": "01a0bbdf-870c-7373-8558-85f4244bb900", "title": "SN1 vs E1 and SN2 vs E2 : The Temperature", "url": "https://www.masterorganicchemistry.com/2012/12/19/sn1-vs-e1-temperature-sn2-vs-e2/", "published_at": "2012-12-19T19:22:15+00:00" }, { "id": "01a0bbdf-870c-7373-8558-85f425f8e91b", "title": "Why Organic Chemistry Made Me Feel Dumb", "url": "https://www.masterorganicchemistry.com/2012/12/05/why-organic-chemistry-made-me-feel-dumb/", "published_at": "2012-12-05T13:16:57+00:00" }, { "id": "01a0bbdf-870c-7373-8558-85f425bd42fe", "title": "Deciding SN1/SN2/E1/E2: The Solvent", "url": "https://www.masterorganicchemistry.com/2012/12/04/deciding-sn1sn2e1e2-the-solvent/", "published_at": "2012-12-04T13:08:08+00:00" }, { "id": "01a0bbcb-bb09-7033-8fb9-c5cf2a273e22", "title": "Deciding SN1/SN2/E1/E2 (2): The Nucleophile/Base", "url": "https://www.masterorganicchemistry.com/2012/11/30/deciding-sn1sn2e1e2-2-the-nucleophilebase/", "published_at": "2012-11-30T17:44:13+00:00" }, { "id": "01a0bb68-8de4-7264-b318-df0218d709b8", "title": "Deciding SN1/SN2/E1/E2 (1): The Substrate", "url": "https://www.masterorganicchemistry.com/2012/11/21/deciding-sn1sn2e1e2-1-the-substrate/", "published_at": "2012-11-21T14:00:12+00:00" }, { "id": "01a0bbe6-04b9-72ce-acd6-e7c2fb0f8c23", "title": "Elimination (E1) Reactions With Rearrangements", "url": "https://www.masterorganicchemistry.com/2012/11/09/e1-reaction-rearrangement/", "published_at": "2012-11-09T14:01:23+00:00" }, { "id": "01a0bbe6-04b9-72ce-acd6-e7c2fab55464", "title": "Comparing the E1 vs SN1 Reactions", "url": 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Rings", "url": "https://www.masterorganicchemistry.com/2012/10/18/the-e2-reaction-and-cyclohexane-rings/", "published_at": "2012-10-18T11:00:28+00:00" }, { "id": "01a0bbe2-d55a-70d8-a91f-267340b10b42", "title": "Introducing the Reaction Guide", "url": "https://www.masterorganicchemistry.com/2012/10/17/introducing-the-reaction-guide/", "published_at": "2012-10-17T18:35:37+00:00" }, { "id": "01a0bbe2-d55a-70d8-a91f-2673418d8293", "title": "E1 vs E2: Comparing the E1 and E2 Reactions", "url": "https://www.masterorganicchemistry.com/2012/10/10/comparing-the-e1-and-e2-reactions/", "published_at": "2012-10-10T11:00:28+00:00" }, { "id": "01a0bbe2-d55a-70d8-a91f-2673416a06e2", "title": "The E2 Mechanism", "url": "https://www.masterorganicchemistry.com/2012/09/27/the-e2-mechanism/", "published_at": "2012-09-27T21:50:13+00:00" }, { "id": "01a0bbe2-d55a-70d8-a91f-2673408335d5", "title": "The E1 Reaction", "url": "https://www.masterorganicchemistry.com/2012/09/19/the-e1-reaction/", "published_at": "2012-09-19T11:16:21+00:00" }, { "id": "01a0bbe2-d55a-70d8-a91f-26733fd33679", "title": "Two Elimination Reaction Patterns", "url": "https://www.masterorganicchemistry.com/2012/09/12/two-types-of-elimination-reactions/", "published_at": "2012-09-12T17:47:03+00:00" }, { "id": "01a0bbe2-d55a-70d8-a91f-26733f8c65ca", "title": "Elimination Reactions Are Favored By Heat", "url": "https://cdn.masterorganicchemistry.com/2012/09/10/elimination-reactions-are-favored-by-heat/", "published_at": "2012-09-10T16:02:15+00:00" }, { "id": "01a0bbdf-870c-7373-8558-85f428361e5d", "title": "Elimination Reactions (2): The Zaitsev Rule", "url": "https://www.masterorganicchemistry.com/2012/08/31/elimination-reactions-2-zaitsevs-rule/", "published_at": "2012-08-31T19:54:28+00:00" }, { "id": "01a0bb68-8de4-7264-b318-df021aed39c7", "title": "Elimination Reactions (1): Introduction And The Key Pattern", "url": "https://www.masterorganicchemistry.com/2012/08/28/walkthrough-of-elimination-reactions-1/", "published_at": "2012-08-28T18:28:46+00:00" }, { "id": "01a0bbe6-04b9-72ce-acd6-e7c2fc1f488d", "title": "Carbocation Rearrangement Reactions (2): Alkyl Shifts", "url": "https://www.masterorganicchemistry.com/2012/08/22/rearrangement-reactions-2-alkyl-shifts/", "published_at": "2012-08-22T08:49:33+00:00" }, { "id": "01a0bbe6-04b9-72ce-acd6-e7c2fcebd061", "title": "Functional Groups Summary Sheet", "url": "https://www.masterorganicchemistry.com/2012/08/21/summary-sheet-functional-groups/", "published_at": "2012-08-21T16:04:42+00:00" }, { "id": "01a0bbb1-b7d9-703b-9fc8-511009166cdb", "title": "Rearrangement Reactions (1): Hydride Shifts", "url": "https://www.masterorganicchemistry.com/2012/08/15/rearrangement-reactions-1-hydride-shifts/", "published_at": "2012-08-15T16:16:52+00:00" } ] posts Claim your blog
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