corpus.blog
41554 blogs · [ { "id": "01a0bb68-8de4-7264-b318-df02176fde38", "title": "The Malonic Ester and Acetoacetic Ester Synthesis", "url": "https://cdn.masterorganicchemistry.com/2012/08/14/the-malonic-ester-synthesis/", "published_at": "2012-08-14T15:09:02+00:00" }, { "id": "01a0bbe6-04b9-72ce-acd6-e7c3001e5cbc", "title": "“America’s Top TA” Shares His Secrets For Teaching O-Chem", "url": "https://www.masterorganicchemistry.com/2012/08/10/americas-top-ta-shares-his-secrets-for-teaching-o-chem/", "published_at": "2012-08-10T18:55:11+00:00" }, { "id": "01a0bbed-7cc0-7271-95ae-806f1eff187c", "title": "Comparing the SN1 and SN2 Reactions", "url": "https://www.masterorganicchemistry.com/2012/08/08/comparing-the-sn1-and-sn2-reactions/", "published_at": "2012-08-08T09:00:44+00:00" }, { "id": "01a0bbed-7cc0-7271-95ae-806f1ca89e9f", "title": "The Conjugate Acid Is A Better Leaving Group", "url": "https://www.masterorganicchemistry.com/2012/08/07/the-conjugate-acid-is-a-better-leaving-group/", "published_at": "2012-08-07T17:10:21+00:00" }, { "id": "01a0bbe6-04b9-72ce-acd6-e7c2ff57537e", "title": "Problem Solving In Organic Chemistry", "url": "https://www.masterorganicchemistry.com/2012/07/23/problem-solving-in-organic-chemistry/", "published_at": "2012-07-23T09:00:50+00:00" }, { "id": "01a0bbd4-9f6e-70ef-8f77-7c980ca30e12", "title": "How John Pulled Up His Organic Chemistry Exam Grades", "url": "https://www.masterorganicchemistry.com/2012/07/18/how-john-pulled-up-his-organic-chemistry-grade/", "published_at": "2012-07-18T23:50:54+00:00" }, { "id": "01a0bbe9-57fc-7307-ad8f-4a4b3e0b94a0", "title": "The SN1 Mechanism", "url": "https://www.masterorganicchemistry.com/2012/07/13/the-sn1-mechanism/", "published_at": "2012-07-13T16:34:14+00:00" }, { "id": "01a0bbe9-57fc-7307-ad8f-4a4b3d16e4bb", "title": "Why the SN2 Reaction Is Powerful", "url": "https://www.masterorganicchemistry.com/2012/07/11/why-the-sn2-reaction-is-powerful/", "published_at": "2012-07-11T19:51:52+00:00" }, { "id": "01a0bbe9-57fc-7307-ad8f-4a4b3bc1e894", "title": "The SN2 Mechanism", "url": "https://www.masterorganicchemistry.com/2012/07/04/the-sn2-mechanism/", "published_at": "2012-07-04T11:10:10+00:00" }, { "id": "01a0bb8b-a298-7227-8668-a6bbb563641d", "title": "Huckels Rule: What Does 4n+2 Mean?", "url": "https://www.masterorganicchemistry.com/2012/06/29/huckels-rule-what-does-4n2-mean/", "published_at": "2012-06-29T09:49:04+00:00" }, { "id": "01a0bbe9-57fc-7307-ad8f-4a4b3b3e63b0", "title": "Two Types of Nucleophilic Substitution Reactions", "url": "https://cdn.masterorganicchemistry.com/2012/06/27/two-types-of-substitution-reactions/", "published_at": "2012-06-27T20:30:41+00:00" }, { "id": "01a0bbe9-57fc-7307-ad8f-4a4b3ea7fb42", "title": "How To Prepare for Organic Chemistry Exams", "url": "https://www.masterorganicchemistry.com/2012/06/22/how-r-m-prepares-for-organic-chemistry-exams/", "published_at": "2012-06-22T16:49:27+00:00" }, { "id": "01a0bbf0-ab8b-7246-9105-d0a3788afd2e", "title": "What Makes A Good Nucleophile?", "url": "https://www.masterorganicchemistry.com/2012/06/18/what-makes-a-good-nucleophile/", "published_at": "2012-06-18T06:45:53+00:00" }, { "id": "01a0bbdb-fc48-70df-8956-f2055162d1a2", "title": "Success Stories: How Nathan Aced Organic Chemistry (Without It Taking Over His Life)", "url": "https://www.masterorganicchemistry.com/2012/06/08/success-stories-how-nathan-aced-organic-chemistry-without-it-taking-over-his-life/", "published_at": "2012-06-08T13:32:28+00:00" }, { "id": "01a0bbf0-ab8b-7246-9105-d0a37788240b", "title": "Nucleophilicity vs. Basicity", "url": "https://www.masterorganicchemistry.com/2012/06/06/nucleophilicity-vs-basicity/", "published_at": "2012-06-06T13:31:57+00:00" }, { "id": "01a0bbed-7cc0-7271-95ae-806f1bdb8fe5", "title": "Nucleophiles and Electrophiles", "url": "https://cdn.masterorganicchemistry.com/2012/06/05/nucleophiles-and-electrophiles/", "published_at": "2012-06-05T22:47:00+00:00" }, { "id": "01a0bbe2-d55a-70d8-a91f-26733f989afc", "title": "Interview: How Jay Got an A+ In Organic Chemistry", "url": "https://www.masterorganicchemistry.com/2012/06/01/interview-how-jay-got-an-a-in-organic-chemistry/", "published_at": "2012-06-01T19:12:50+00:00" }, { "id": "01a0bbe6-04b9-72ce-acd6-e7c2fe87d17b", "title": "Nucleophilic Substitution Reactions – Introduction", "url": "https://www.masterorganicchemistry.com/2012/05/31/walkthrough-of-nucleophilic-substitution-reactions-introduction/", "published_at": "2012-05-31T18:49:14+00:00" }, { "id": "01a0bc13-6086-71a5-841e-6d16c154c117", "title": "How Protonation and Deprotonation Affect Reactivity", "url": "https://www.masterorganicchemistry.com/2012/05/30/acid-base-reactions-whats-the-point/", "published_at": "2012-05-30T08:30:14+00:00" }, { "id": "01a0bbed-7cc0-7271-95ae-806f1d38d309", "title": "Interview: “Taking Organic Chemistry Is A Great Way To Develop Critical Thinking Skills”", "url": "https://www.masterorganicchemistry.com/2012/05/25/organic_chem_instructor_interview/", "published_at": "2012-05-25T14:21:27+00:00" }, { "id": "01a0bc0a-394c-73f3-a874-35b5ad4d094b", "title": "What Is a Racemic Mixture?", "url": "https://www.masterorganicchemistry.com/2012/05/23/whats-a-racemic-mixture/", "published_at": "2012-05-23T16:34:07+00:00" }, { "id": "01a0bc0e-e752-704e-a32e-b287203d6cf1", "title": "Acid Base Reactions Are Fast", "url": "https://www.masterorganicchemistry.com/2012/05/21/acid-base-reactions-are-fast/", "published_at": "2012-05-21T10:26:45+00:00" }, { "id": "01a0bbfd-7955-724d-962f-1473f4e01875", "title": "A Handy Rule of Thumb for Acid-Base Reactions", "url": "https://www.masterorganicchemistry.com/2012/05/17/a-handy-rule-of-thumb-for-acid-base-reactions/", "published_at": "2012-05-17T16:28:00+00:00" }, { "id": "01a0bbf0-ab8b-7246-9105-d0a37478f962", "title": "Acid-Base Reactions: Introducing Ka and pKa", "url": "https://cdn.masterorganicchemistry.com/2012/05/09/acid-base-reactions-ka-and-pka/", "published_at": "2012-05-09T18:43:20+00:00" }, { "id": "01a0bbed-7cc0-7271-95ae-806f1eb2bf9d", "title": "Organic Chemistry Study Tips: Reaction Maps", "url": "https://www.masterorganicchemistry.com/2012/05/07/organic-chemistry-study-tips-reaction-maps/", "published_at": "2012-05-07T08:54:21+00:00" }, { "id": "01a0bbfd-7955-724d-962f-1473f38768a4", "title": "Polar Protic? Polar Aprotic? Nonpolar? All About Solvents", "url": "https://www.masterorganicchemistry.com/2012/04/27/polar-protic-polar-aprotic-nonpolar-all-about-solvents/", "published_at": "2012-04-27T17:31:42+00:00" }, { "id": "01a0bba2-2769-7397-8f07-33a72613bed9", "title": "Homotopic, Enantiotopic, Diastereotopic", "url": "https://www.masterorganicchemistry.com/2012/04/17/homotopic-enantiotopic-diastereotopic/", "published_at": "2012-04-17T20:36:31+00:00" }, { "id": "01a0bbed-7cc0-7271-95ae-806f1e89bc59", "title": "Factors That Affect Base Strength In Organic Chemistry", "url": "https://www.masterorganicchemistry.com/2012/04/16/basicity-trends-organic-chemistry/", "published_at": "2012-04-16T15:47:46+00:00" }, { "id": "01a0bbed-7cc0-7271-95ae-806f1ce7d9ff", "title": "Acid Base Reactions In Organic Chemistry", "url": "https://www.masterorganicchemistry.com/2012/04/11/walkthrough-of-acid-base-reactions-1/", "published_at": "2012-04-11T09:16:01+00:00" }, { "id": "01a0bb5a-3ba0-71ad-ab84-d3e35594f683", "title": "What Is The Alpha Carbon In Carbonyl Compounds?", "url": "https://www.masterorganicchemistry.com/2012/03/26/weird-nomenclature-in-carbonyl-chemistry/", "published_at": "2012-03-26T11:12:24+00:00" }, { "id": "01a0bbfd-7955-724d-962f-1473f1b69431", "title": "7 Factors That Stabilize Positive Charge in Organic Chemistry", "url": "https://cdn.masterorganicchemistry.com/2012/03/07/7-factors-that-stabilize-positive-charge-in-organic-chemistry/", "published_at": "2012-03-07T22:51:10+00:00" }, { "id": "01a0bbf9-63fe-72a3-b2f3-8dd51d296714", "title": "7 Factors that stabilize negative charge in organic chemistry", "url": "https://www.masterorganicchemistry.com/2012/02/27/7-factors-that-stabilize-negative-charge-in-organic-chemistry/", "published_at": "2012-02-28T02:13:33+00:00" }, { "id": "01a0bb53-d47c-7111-a867-f975dd61e74b", "title": "Common Mistakes: Formal Charges Can Mislead", "url": "https://www.masterorganicchemistry.com/2012/02/22/common-mistakes-formal-charges-can-mislead/", "published_at": "2012-02-22T23:06:34+00:00" }, { "id": "01a0bbf3-9b35-73c6-b6a7-4c3ea7b049db", "title": "Organic Chemistry Study Tips: How to use a “Study Buddy”", "url": "https://cdn.masterorganicchemistry.com/2012/02/16/organic-chemistry-study-tips-how-to-use-a-study-buddy/", "published_at": "2012-02-16T12:00:28+00:00" }, { "id": "01a0bbe9-57fc-7307-ad8f-4a4b3e8fdab3", "title": "Curved Arrows (for reactions)", "url": "https://www.masterorganicchemistry.com/2012/02/15/curved-arrows-for-reactions/", "published_at": "2012-02-15T22:07:17+00:00" }, { "id": "01a0bb77-6bbf-7016-a192-bcf99824fa31", "title": "Thermodynamic and Kinetic Products", "url": "https://www.masterorganicchemistry.com/2012/02/09/kinetic-thermodynamic-products-can-openers/", "published_at": "2012-02-09T09:00:33+00:00" }, { "id": "01a0bbf3-9b35-73c6-b6a7-4c3ea99e2be5", "title": "Take “Don’t Memorize!” with a grain of salt", "url": "https://www.masterorganicchemistry.com/2012/01/19/take-dont-memorize-with-a-grain-of-salt/", "published_at": "2012-01-19T22:59:40+00:00" }, { "id": "01a0bc0e-e752-704e-a32e-b28721ae78ac", "title": "How to apply electronegativity and resonance to understand reactivity", "url": "https://www.masterorganicchemistry.com/2012/01/17/how-to-apply-electronegativity-and-resonance-to-understand-reactivity/", "published_at": "2012-01-17T06:02:58+00:00" }, { "id": "01a0bc0e-e752-704e-a32e-b2871ffdfb8c", "title": "Drawing Resonance Structures: 3 Common Mistakes To Avoid", "url": "https://www.masterorganicchemistry.com/2012/01/10/common-mistakes-how-not-to-draw-resonance-curved-arrows/", "published_at": "2012-01-10T18:00:14+00:00" }, { "id": "01a0bc0e-e752-704e-a32e-b2871d6a8551", "title": "In Summary: How To Evaluate Resonance Structures", "url": "https://www.masterorganicchemistry.com/2011/12/22/in-summary-resonance/", "published_at": "2011-12-22T16:20:18+00:00" }, { "id": "01a0bc0c-9933-73f4-9a10-ab2a3b800c2a", "title": "Exploring Resonance: Pi-acceptors", "url": "https://www.masterorganicchemistry.com/2011/12/19/exploring-resonance-pi-acceptors/", "published_at": "2011-12-19T12:00:21+00:00" }, { "id": "01a0bc02-c36b-7331-96b8-b5ed4aa13421", "title": "Pi-Donation and Pi-Donors", "url": "https://www.masterorganicchemistry.com/2011/12/15/exploring-resonance-pi-donation/", "published_at": "2011-12-15T12:00:54+00:00" }, { "id": "01a0bbf6-87a8-71d3-b41a-f345946e599c", "title": "Resonance Structures Should Have Full Octets (If Possible!)", "url": "https://www.masterorganicchemistry.com/2011/12/14/resonance-structures-full-octets-carbocations/", "published_at": "2011-12-14T12:00:35+00:00" }, { "id": "01a0bbf6-87a8-71d3-b41a-f3459577adaa", "title": "Resonance Structures: Negative Charges Are Best Placed On The Least Basic Atom", "url": "https://www.masterorganicchemistry.com/2011/12/13/resonance-structure-negative-charge-least-basic-atom/", "published_at": "2011-12-13T12:00:39+00:00" }, { "id": "01a0bbf6-87a8-71d3-b41a-f345933da197", "title": "How To Find The Best Resonance Structure By Applying Electronegativity", "url": "https://www.masterorganicchemistry.com/2011/12/12/evaluating-resonance-structures-2-applying-electronegativity/", "published_at": "2011-12-12T12:00:09+00:00" }, { "id": "01a0bbf6-87a8-71d3-b41a-f345917b0dbf", "title": "Evaluating Resonance Structures: The Fewer Charges, The Better", "url": "https://www.masterorganicchemistry.com/2011/12/08/evaluating-resonance-forms-1-the-rule-of-least-charges/", "published_at": "2011-12-08T12:00:59+00:00" }, { "id": "01a0bc07-d508-7179-9466-6104e41c088a", "title": "The Principle of Least Effort", "url": "https://www.masterorganicchemistry.com/2011/12/07/the-principle-of-least-effort/", "published_at": "2011-12-07T12:00:48+00:00" }, { "id": "01a0bc05-5098-72fb-9afc-68b47bcd8314", "title": "Thionyl Chloride (SOCl2) And Conversion of Carboxylic Acids to Acid Halides", "url": "https://www.masterorganicchemistry.com/2011/12/03/reagent-friday-thionyl-chloride-socl2/", "published_at": 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"01a0bbf9-63fe-72a3-b2f3-8dd51b988c00", "title": "“Compare Organic Chemistry To A Movie…”", "url": "https://www.masterorganicchemistry.com/2011/10/19/compare-organic-chemistry-to-a-movie/", "published_at": "2011-10-19T12:00:05+00:00" }, { "id": "01a0bb5a-3ba0-71ad-ab84-d3e3533c8bcb", "title": "Introduction to Rearrangement Reactions", "url": "https://cdn.masterorganicchemistry.com/2011/10/17/introduction-to-rearrangement-reactions/", "published_at": "2011-10-17T12:00:39+00:00" }, { "id": "01a0bbf0-ab8b-7246-9105-d0a376e4a96c", "title": "Grignard Reagents For Addition To Aldehydes and Ketones", "url": "https://www.masterorganicchemistry.com/2011/10/14/reagent-friday-grignard-reagents/", "published_at": "2011-10-14T22:25:25+00:00" }, { "id": "01a0bbf9-63fe-72a3-b2f3-8dd51e00eaa5", "title": "Reagent Friday: Sodium (Na)", "url": "https://www.masterorganicchemistry.com/2011/10/07/reagent-friday-sodium-na/", "published_at": "2011-10-07T08:27:51+00:00" }, { "id": "01a0bc05-5098-72fb-9afc-68b476ac0be1", "title": "Grossman’s Rule", "url": "https://cdn.masterorganicchemistry.com/2011/10/06/grossmans-rule/", "published_at": "2011-10-06T08:30:33+00:00" }, { "id": "01a0bbfd-7955-724d-962f-1473f1b94be3", "title": "Reagent Friday: Raney Nickel", "url": "https://www.masterorganicchemistry.com/2011/09/30/reagent-friday-raney-nickel/", "published_at": "2011-09-30T18:53:01+00:00" }, { "id": "01a0bbfd-7955-724d-962f-1473f6644b8c", "title": "Hammonds Postulate", "url": "https://www.masterorganicchemistry.com/2011/09/28/hammonds-postulate/", "published_at": "2011-09-28T17:00:03+00:00" }, { "id": "01a0bbfd-7955-724d-962f-1473f2b3da2b", "title": "Blog Carnival: What the Cope Rearrangement Taught Me About Chemistry", "url": "https://www.masterorganicchemistry.com/2011/09/26/blog-carnival-what-the-cope-rearrangement-taught-me-about-chemistry/", "published_at": "2011-09-27T02:59:13+00:00" }, { "id": "01a0bbfd-7955-724d-962f-1473f45ebf79", "title": "How to Get An A In Organic Chemistry", "url": "https://www.masterorganicchemistry.com/2011/09/21/advice-from-a-students/", "published_at": "2011-09-21T08:44:39+00:00" }, { "id": "01a0bbdf-870c-7373-8558-85f4238c71c6", "title": "Introduction to Acid-Base Reactions", "url": "https://www.masterorganicchemistry.com/2011/09/19/introduction-to-acid-base-reactions/", "published_at": "2011-09-19T09:07:40+00:00" }, { "id": "01a0bbfd-7955-724d-962f-1473f549fedb", "title": "“Reagents”: A Pocket Encyclopedia of Reagents for Organic Chemistry", "url": "https://www.masterorganicchemistry.com/2011/09/13/reagents-a-pocket-encyclopedia-of-reagents-for-organic-chemistry/", "published_at": "2011-09-13T12:58:23+00:00" }, { "id": "01a0bbfd-7955-724d-962f-1473f6152561", "title": "Reagent Friday: PCC (Pyridinium Chlorochromate)", "url": "https://www.masterorganicchemistry.com/2011/09/09/reagent-friday-pcc-pyridinium-chlorochromate/", "published_at": "2011-09-09T18:08:59+00:00" }, { "id": "01a0bbf3-9b35-73c6-b6a7-4c3eaa36749d", "title": "The 4 Major Classes of Reactions in Org 1", "url": "https://www.masterorganicchemistry.com/2011/09/05/the-4-major-classes-of-reactions-in-org-1/", "published_at": "2011-09-05T13:40:07+00:00" }, { "id": "01a0bb53-d47c-7111-a867-f975e01ae785", "title": "The Most Important Question To Ask When Learning a New Reaction", "url": "https://www.masterorganicchemistry.com/2011/08/29/what-bonds-form-what-bonds-break/", "published_at": "2011-08-29T14:20:51+00:00" }, { "id": "01a0bc00-1d8c-7251-9e5b-7a469adc15f6", "title": "Di-isobutyl Aluminum Hydride (DIBAL) For The Partial Reduction of Esters and Nitriles", "url": "https://www.masterorganicchemistry.com/2011/08/26/dibal-di-isobutyl-aluminum-hydride/", "published_at": "2011-08-26T19:11:43+00:00" }, { "id": "01a0bc00-1d8c-7251-9e5b-7a469b2c3abb", "title": "How (and why) electrons flow", "url": "https://www.masterorganicchemistry.com/2011/08/24/how-and-why-electrons-flow/", "published_at": "2011-08-24T11:56:33+00:00" }, { "id": "01a0bc00-1d8c-7251-9e5b-7a469b6bcf51", "title": "Instructor’s “kludges” of organic chemistry", "url": "https://www.masterorganicchemistry.com/2011/08/22/instructors-kludges-of-organic-chemistry/", "published_at": "2011-08-22T14:12:40+00:00" }, { "id": "01a0bbcb-bb09-7033-8fb9-c5cf2887bca5", "title": "Partial Reduction of Alkynes With Lindlar Catalyst", "url": "https://www.masterorganicchemistry.com/2011/08/19/lindlars-catalyst-partial-cis-reduction/", "published_at": "2011-08-19T13:43:58+00:00" }, { "id": "01a0bc00-1d8c-7251-9e5b-7a469bf15530", "title": "Summary Sheet #8: The Oxidation Ladder", "url": "https://www.masterorganicchemistry.com/2011/08/15/summary-sheet-8-the-oxidation-ladder/", "published_at": "2011-08-15T13:03:30+00:00" }, { "id": "01a0bb7e-d2f8-709a-9e06-25b8a61ae6b6", "title": "Sodium Borohydride (NaBH4) Reduction of Aldehydes and Ketones", "url": "https://www.masterorganicchemistry.com/2011/08/12/reagent-friday-sodium-borohydride-nabh4/", "published_at": "2011-08-12T19:16:43+00:00" }, { "id": "01a0bc00-1d8c-7251-9e5b-7a469cc8c48d", "title": "The Lies We Tell", "url": "https://www.masterorganicchemistry.com/2011/08/10/the-lies-we-tell/", "published_at": "2011-08-10T13:51:38+00:00" }, { "id": "01a0bc00-1d8c-7251-9e5b-7a469cf44f94", "title": "Oxidation Ladders", "url": "https://www.masterorganicchemistry.com/2011/08/08/oxidation-ladders/", "published_at": "2011-08-08T12:30:08+00:00" }, { "id": "01a0bbcb-bb09-7033-8fb9-c5cf276e2ad5", "title": "Oxidation and Reduction in Organic Chemistry", "url": "https://www.masterorganicchemistry.com/2011/08/01/oxidation-and-reduction-in-organic-chemistry/", "published_at": "2011-08-01T13:39:26+00:00" }, { "id": "01a0bc00-1d8c-7251-9e5b-7a469d422f7a", "title": "Reagent Friday: Sodium Amide (NaNH2)", "url": "https://www.masterorganicchemistry.com/2011/07/29/reagent-friday-sodium-amide-nanh2-2/", "published_at": "2011-07-29T16:45:23+00:00" }, { "id": "01a0bbbb-e0e0-7054-8b0e-5c2ffc6a4f88", "title": "Calculating the oxidation state of a carbon", "url": "https://www.masterorganicchemistry.com/2011/07/25/calculating-the-oxidation-state-of-a-carbon/", "published_at": "2011-07-25T13:27:23+00:00" }, { "id": "01a0bc02-c36b-7331-96b8-b5ed4a36fcb8", "title": "Steric Hindrance is Like a Fat Goalie", "url": "https://www.masterorganicchemistry.com/2011/07/18/steric-hindrance-is-like-a-fat-goalie/", "published_at": "2011-07-18T13:40:27+00:00" }, { "id": "01a0bb53-d47c-7111-a867-f975ddf8e5e0", "title": "Partial Charges Give Clues About Electron Flow", "url": "https://www.masterorganicchemistry.com/2011/07/11/partial-charges/", "published_at": "2011-07-11T13:32:27+00:00" }, { "id": "01a0bc02-c36b-7331-96b8-b5ed4b33fcbf", "title": "Common Blind Spot: Intramolecular Reactions", "url": "https://www.masterorganicchemistry.com/2011/07/04/common-blind-spot-intramolecular-reactions/", "published_at": "2011-07-04T14:10:42+00:00" }, { "id": "01a0bbdb-fc48-70df-8956-f2054f8f7271", "title": "OsO4 (Osmium Tetroxide) for Dihydroxylation of Alkenes", "url": "https://www.masterorganicchemistry.com/2011/07/01/reagent-friday-oso4-osmium-tetroxide/", "published_at": "2011-07-01T14:11:19+00:00" }, { "id": "01a0bbf9-63fe-72a3-b2f3-8dd5193b1130", "title": "Hidden Hydrogens, Hidden Lone Pairs, Hidden Counterions", "url": "https://cdn.masterorganicchemistry.com/2011/06/27/hidden-hydrogens-hidden-lone-pairs-hidden-counterions/", "published_at": "2011-06-27T14:00:18+00:00" }, { "id": "01a0bbdb-fc48-70df-8956-f2054d848e42", "title": "Condensed Formulas: Deciphering What the Brackets Mean", "url": "https://www.masterorganicchemistry.com/2011/06/20/condensed-structural-formulas/", "published_at": "2011-06-20T13:38:07+00:00" }, { "id": "01a0bbdb-fc48-70df-8956-f2054ead6d45", "title": "m-CPBA (meta-chloroperoxybenzoic acid)", "url": "https://www.masterorganicchemistry.com/2011/06/17/reagent-friday-m-cpba-meta-chloroperoxybenzoic-acid/", "published_at": "2011-06-17T14:20:34+00:00" }, { "id": "01a0bc02-c36b-7331-96b8-b5ed4d55a584", "title": "Reagent Friday: NBS (N-Bromo Succinimide)", "url": "https://www.masterorganicchemistry.com/2011/06/10/reagent-friday-nbs-n-bromo-succinimide/", "published_at": "2011-06-10T13:29:44+00:00" }, { "id": "01a0bc02-c36b-7331-96b8-b5ed4dc281e1", "title": "Reagent Friday: Chromic Acid, H2CrO4", "url": "https://www.masterorganicchemistry.com/2011/06/03/reagent-friday-chromic-acid-h2cro4/", "published_at": "2011-06-03T14:00:37+00:00" }, { "id": "01a0bb53-d47c-7111-a867-f975de4717ea", "title": "Draw The Ugly Version First", "url": "https://www.masterorganicchemistry.com/2011/05/31/draw-the-ugly-version-first/", "published_at": "2011-05-31T12:40:18+00:00" }, { "id": "01a0bc05-5098-72fb-9afc-68b476fcdab9", "title": "The Organic Chemistry Reagent Guide is here!", "url": "https://www.masterorganicchemistry.com/2011/05/26/the-organic-chemistry-reagent-guide-is-here/", "published_at": "2011-05-26T16:05:18+00:00" }, { "id": "01a0bbc4-be67-7197-8e53-a9987583a792", "title": "Common Mistakes with Carbonyls: Carboxylic Acids… Are Acids!", "url": "https://www.masterorganicchemistry.com/2011/05/20/common-mistakes-with-carbonyls-carboxylic-acids-are-acids/", "published_at": "2011-05-20T22:26:39+00:00" }, { "id": "01a0bb53-d47c-7111-a867-f975dcb54859", "title": "Nucleophilic Acyl Substitution (With Negatively Charged Nucleophiles)", "url": "https://www.masterorganicchemistry.com/2011/05/06/nucleophilic-acyl-substitution/", "published_at": "2011-05-06T18:37:45+00:00" }, { "id": "01a0bbf0-ab8b-7246-9105-d0a37811ff67", "title": "Number Your Carbons!", "url": "https://www.masterorganicchemistry.com/2011/04/15/if-youre-leaving-for-an-exam-in-3-minutes-or-less-read-this/", "published_at": "2011-04-15T14:32:10+00:00" }, { "id": "01a0bc05-5098-72fb-9afc-68b47a610fd0", "title": "Why organic chemistry is hard (2)", "url": "https://www.masterorganicchemistry.com/2011/04/14/why-organic-chemistry-is-hard-2/", "published_at": "2011-04-14T12:00:44+00:00" }, { "id": "01a0bbf0-ab8b-7246-9105-d0a3791e723f", "title": "What Makes A Good Leaving Group?", "url": "https://www.masterorganicchemistry.com/2011/04/12/what-makes-a-good-leaving-group/", "published_at": "2011-04-12T12:13:02+00:00" } ] posts Claim your blog
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jamesash

masterorganicchemistry.com

2012

The Malonic Ester and Acetoacetic Ester Synthesisoriginal ↗
14 Aug 2012
“America’s Top TA” Shares His Secrets For Teaching O-Chemoriginal ↗
10 Aug 2012
Comparing the SN1 and SN2 Reactionsoriginal ↗
8 Aug 2012
The Conjugate Acid Is A Better Leaving Grouporiginal ↗
7 Aug 2012
Problem Solving In Organic Chemistryoriginal ↗
23 Jul 2012
How John Pulled Up His Organic Chemistry Exam Gradesoriginal ↗
18 Jul 2012
The SN1 Mechanismoriginal ↗
13 Jul 2012
Why the SN2 Reaction Is Powerfuloriginal ↗
11 Jul 2012
The SN2 Mechanismoriginal ↗
4 Jul 2012
Huckels Rule: What Does 4n+2 Mean?original ↗
29 Jun 2012
Two Types of Nucleophilic Substitution Reactionsoriginal ↗
27 Jun 2012
How To Prepare for Organic Chemistry Examsoriginal ↗
22 Jun 2012
What Makes A Good Nucleophile?original ↗
18 Jun 2012
Success Stories: How Nathan Aced Organic Chemistry (Without It Taking Over His Life)original ↗
8 Jun 2012
Nucleophilicity vs. Basicityoriginal ↗
6 Jun 2012
Nucleophiles and Electrophilesoriginal ↗
5 Jun 2012
Interview: How Jay Got an A+ In Organic Chemistryoriginal ↗
1 Jun 2012
Nucleophilic Substitution Reactions – Introductionoriginal ↗
31 May 2012
How Protonation and Deprotonation Affect Reactivityoriginal ↗
30 May 2012
Interview: “Taking Organic Chemistry Is A Great Way To Develop Critical Thinking Skills”original ↗
25 May 2012
What Is a Racemic Mixture?original ↗
23 May 2012
Acid Base Reactions Are Fastoriginal ↗
21 May 2012
A Handy Rule of Thumb for Acid-Base Reactionsoriginal ↗
17 May 2012
Acid-Base Reactions: Introducing Ka and pKaoriginal ↗
9 May 2012
Organic Chemistry Study Tips: Reaction Mapsoriginal ↗
7 May 2012
Polar Protic? Polar Aprotic? Nonpolar? All About Solventsoriginal ↗
27 Apr 2012
Homotopic, Enantiotopic, Diastereotopicoriginal ↗
17 Apr 2012
Factors That Affect Base Strength In Organic Chemistryoriginal ↗
16 Apr 2012
Acid Base Reactions In Organic Chemistryoriginal ↗
11 Apr 2012
What Is The Alpha Carbon In Carbonyl Compounds?original ↗
26 Mar 2012
7 Factors That Stabilize Positive Charge in Organic Chemistryoriginal ↗
7 Mar 2012
7 Factors that stabilize negative charge in organic chemistryoriginal ↗
28 Feb 2012
Common Mistakes: Formal Charges Can Misleadoriginal ↗
22 Feb 2012
Organic Chemistry Study Tips: How to use a “Study Buddy”original ↗
16 Feb 2012
Curved Arrows (for reactions)original ↗
15 Feb 2012
Thermodynamic and Kinetic Productsoriginal ↗
9 Feb 2012
Take “Don’t Memorize!” with a grain of saltoriginal ↗
19 Jan 2012
How to apply electronegativity and resonance to understand reactivityoriginal ↗
17 Jan 2012
Drawing Resonance Structures: 3 Common Mistakes To Avoidoriginal ↗
10 Jan 2012

2011

In Summary: How To Evaluate Resonance Structuresoriginal ↗
22 Dec 2011
Exploring Resonance: Pi-acceptorsoriginal ↗
19 Dec 2011
Pi-Donation and Pi-Donorsoriginal ↗
15 Dec 2011
Resonance Structures Should Have Full Octets (If Possible!)original ↗
14 Dec 2011
Resonance Structures: Negative Charges Are Best Placed On The Least Basic Atomoriginal ↗
13 Dec 2011
How To Find The Best Resonance Structure By Applying Electronegativityoriginal ↗
12 Dec 2011
Evaluating Resonance Structures: The Fewer Charges, The Betteroriginal ↗
8 Dec 2011
The Principle of Least Effortoriginal ↗
7 Dec 2011
Thionyl Chloride (SOCl2) And Conversion of Carboxylic Acids to Acid Halidesoriginal ↗
3 Dec 2011
How To Use Curved Arrows To Interconvert Resonance Structuresoriginal ↗
30 Nov 2011
Palladium on Carbon (Pd/C) for Catalytic Hydrogenation of Alkenesoriginal ↗
25 Nov 2011
Introduction to Resonanceoriginal ↗
23 Nov 2011
Organic Chemistry Is Shitoriginal ↗
18 Nov 2011
How To Use Electronegativity To Determine Electron Density (and why NOT to trust formal charge)original ↗
15 Nov 2011
LiAlH[Ot-Bu]3 For The Reduction of Acid Halides To Aldehydesoriginal ↗
11 Nov 2011
Don’t Be Futyl, Learn The Butylsoriginal ↗
10 Nov 2011
Diazomethane (CH2N2)original ↗
5 Nov 2011
Reagent Friday: Potassium tert-butoxide [KOC(CH3)3]original ↗
29 Oct 2011
Guest post: “I went from being afraid of tests to actually looking forward to them”.original ↗
26 Oct 2011
Oxidative Cleavage of Vicinal Diols With NaIO4 and Pb(OAc)4original ↗
21 Oct 2011
“Compare Organic Chemistry To A Movie…”original ↗
19 Oct 2011
Introduction to Rearrangement Reactionsoriginal ↗
17 Oct 2011
Grignard Reagents For Addition To Aldehydes and Ketonesoriginal ↗
14 Oct 2011
Reagent Friday: Sodium (Na)original ↗
7 Oct 2011
Grossman’s Ruleoriginal ↗
6 Oct 2011
Reagent Friday: Raney Nickeloriginal ↗
30 Sept 2011
Hammonds Postulateoriginal ↗
28 Sept 2011
Blog Carnival: What the Cope Rearrangement Taught Me About Chemistryoriginal ↗
27 Sept 2011
How to Get An A In Organic Chemistryoriginal ↗
21 Sept 2011
Introduction to Acid-Base Reactionsoriginal ↗
19 Sept 2011
“Reagents”: A Pocket Encyclopedia of Reagents for Organic Chemistryoriginal ↗
13 Sept 2011
Reagent Friday: PCC (Pyridinium Chlorochromate)original ↗
9 Sept 2011
The 4 Major Classes of Reactions in Org 1original ↗
5 Sept 2011
The Most Important Question To Ask When Learning a New Reactionoriginal ↗
29 Aug 2011
Di-isobutyl Aluminum Hydride (DIBAL) For The Partial Reduction of Esters and Nitrilesoriginal ↗
26 Aug 2011
How (and why) electrons floworiginal ↗
24 Aug 2011
Instructor’s “kludges” of organic chemistryoriginal ↗
22 Aug 2011
Partial Reduction of Alkynes With Lindlar Catalystoriginal ↗
19 Aug 2011
Summary Sheet #8: The Oxidation Ladderoriginal ↗
15 Aug 2011
Sodium Borohydride (NaBH4) Reduction of Aldehydes and Ketonesoriginal ↗
12 Aug 2011
The Lies We Telloriginal ↗
10 Aug 2011
Oxidation Laddersoriginal ↗
8 Aug 2011
Oxidation and Reduction in Organic Chemistryoriginal ↗
1 Aug 2011
Reagent Friday: Sodium Amide (NaNH2)original ↗
29 Jul 2011
Calculating the oxidation state of a carbonoriginal ↗
25 Jul 2011
Steric Hindrance is Like a Fat Goalieoriginal ↗
18 Jul 2011
Partial Charges Give Clues About Electron Floworiginal ↗
11 Jul 2011
Common Blind Spot: Intramolecular Reactionsoriginal ↗
4 Jul 2011
OsO4 (Osmium Tetroxide) for Dihydroxylation of Alkenesoriginal ↗
1 Jul 2011
Hidden Hydrogens, Hidden Lone Pairs, Hidden Counterionsoriginal ↗
27 Jun 2011
Condensed Formulas: Deciphering What the Brackets Meanoriginal ↗
20 Jun 2011
m-CPBA (meta-chloroperoxybenzoic acid)original ↗
17 Jun 2011
Reagent Friday: NBS (N-Bromo Succinimide)original ↗
10 Jun 2011
Reagent Friday: Chromic Acid, H2CrO4original ↗
3 Jun 2011
Draw The Ugly Version Firstoriginal ↗
31 May 2011
The Organic Chemistry Reagent Guide is here!original ↗
26 May 2011
Common Mistakes with Carbonyls: Carboxylic Acids… Are Acids!original ↗
20 May 2011
Nucleophilic Acyl Substitution (With Negatively Charged Nucleophiles)original ↗
6 May 2011
Number Your Carbons!original ↗
15 Apr 2011
Why organic chemistry is hard (2)original ↗
14 Apr 2011
What Makes A Good Leaving Group?original ↗
12 Apr 2011
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