{"product_id":"organic-chemistry-2","title":"Organic Chemistry 2 - 1 session","description":"\u003cp data-path-to-node=\"0\"\u003eOrganic Chemistry 2 is widely considered the \"reactions\" semester. While Organic Chemistry 1 focuses on the fundamental laws of bonding and 3D space, the second semester moves into the complex world of aromaticity, carbonyl chemistry, and the building blocks of life (biomolecules).\u003c\/p\u003e\n\u003ch2 data-path-to-node=\"1\"\u003eOrganic Chemistry 2 Syllabus\u003c\/h2\u003e\n\u003ch3 data-path-to-node=\"2\"\u003eUnit 1: Conjugated Systems and Pericyclic Reactions\u003c\/h3\u003e\n\u003cul data-path-to-node=\"3\"\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"3,0,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"3,0,0\"\u003eConjugation and Resonance:\u003c\/b\u003e Stability of the allyl cation and radical.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"3,1,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"3,1,0\"\u003eDienes:\u003c\/b\u003e Understanding 1,2-addition versus 1,4-addition (kinetic vs. thermodynamic control).\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"3,2,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"3,2,0\"\u003eThe Diels-Alder Reaction:\u003c\/b\u003e A [4+2] cycloaddition used to create six-membered rings.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr data-path-to-node=\"4\"\u003e\n\u003ch3 data-path-to-node=\"5\"\u003eUnit 2: Aromaticity and Benzene\u003c\/h3\u003e\n\u003cul data-path-to-node=\"6\"\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"6,0,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"6,0,0\"\u003eAromaticity Criteria:\u003c\/b\u003e Hückel’s Rule (\u003cspan data-index-in-node=\"37\" data-math=\"4n+2\" class=\"math-inline\"\u003e4n+2\u003c\/span\u003epi electrons) and the requirement for a planar, cyclic, conjugated system.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"6,1,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"6,1,0\"\u003eNaming Benzene Derivatives:\u003c\/b\u003e Using ortho, meta, and para descriptors.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp id=\"p-rc_a30fa7ae80bd6935-69\" data-path-to-node=\"6,2,0\"\u003e\u003cspan class=\"citation-90\"\u003e\u003c\/span\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"6,2,0\"\u003e\u003cspan class=\"citation-90\"\u003eElectrophilic Aromatic Substitution (EAS):\u003c\/span\u003e\u003c\/b\u003e\u003cspan class=\"citation-90 citation-end-90\"\u003e Mechanisms for nitration, sulfonation, halogenation, and Friedel-Crafts alkylation\/acylation.\u003csup data-turn-source-index=\"1\" class=\"superscript\"\u003e\u003c!----\u003e\u003c\/sup\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"source-inline-chip-container ng-star-inserted\"\u003e\n\u003c!----\u003e\u003cbutton data-ved=\"0CAAQvoAQahgKEwjd-ZWUm_-TAxUAAAAAHQAAAAAQ2AE\" data-hveid=\"0\" aria-label=\"View source details for citation from SGU Course Catalogs and Handbooks - St. George's University. Opens side panel.\" class=\"button ng-star-inserted\"\u003e\u003c!----\u003e\u003c!----\u003e\u003c\/button\u003e\u003c!----\u003e\u003c!----\u003e\u003c!----\u003e\n\u003c\/div\u003e\n\u003c!----\u003e\u003c!----\u003e\u003c!----\u003e\u003c!----\u003e\u003c!----\u003e\u003c!----\u003e\u003c!----\u003e\u003c!----\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"6,3,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"6,3,0\"\u003eSubstituent Effects:\u003c\/b\u003e How \"activating\" and \"deactivating\" groups direct new groups to specific positions on the ring.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-path-to-node=\"7\"\u003eUnit 3: Aldehydes and Ketones\u003c\/h3\u003e\n\u003cul data-path-to-node=\"8\"\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"8,0,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"8,0,0\"\u003eNucleophilic Addition:\u003c\/b\u003e The core reactivity pattern of the \u003cspan data-index-in-node=\"58\" data-math=\"C=O\" class=\"math-inline\"\u003e$C=O$\u003c\/span\u003e bond.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"8,1,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"8,1,0\"\u003eKey Reactions:\u003c\/b\u003e Formation of acetals, hemiacetals, imines, and enamines.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"8,2,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"8,2,0\"\u003eThe Wittig Reaction:\u003c\/b\u003e A powerful method for turning a carbonyl into a carbon-carbon double bond.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr data-path-to-node=\"9\"\u003e\n\u003ch3 data-path-to-node=\"10\"\u003eUnit 4: Carboxylic Acids and Their Derivatives\u003c\/h3\u003e\n\u003cul data-path-to-node=\"11\"\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"11,0,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"11,0,0\"\u003eNucleophilic Acyl Substitution:\u003c\/b\u003e The mechanism for converting one derivative into another.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"11,1,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"11,1,0\"\u003eThe \"Reactivity Ladder\":\u003c\/b\u003e Why acid chlorides are more reactive than esters, which are more reactive than amides.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"11,2,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"11,2,0\"\u003eHydrolysis and Saponification:\u003c\/b\u003e Breaking down esters and amides with acid or base (the chemistry of soap making).\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-path-to-node=\"12\"\u003eUnit 5: Alpha-Substitution and Condensations\u003c\/h3\u003e\n\u003cul data-path-to-node=\"13\"\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"13,0,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"13,0,0\"\u003eEnols and Enolates:\u003c\/b\u003e Understanding the acidity of the alpha-hydrogen.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"13,1,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"13,1,0\"\u003eThe Aldol Reaction:\u003c\/b\u003e Combining two carbonyls to form b\u003cspan data-index-in-node=\"52\" data-math=\"\\beta\" class=\"math-inline\"\u003eeta\u003c\/span\u003e-hydroxy carbonyls.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"13,2,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"13,2,0\"\u003eThe Claisen Condensation:\u003c\/b\u003e The ester version of the Aldol reaction.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"13,3,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"13,3,0\"\u003eMalonic and Acetoacetic Ester Synthesis:\u003c\/b\u003e Classic methods for building custom carboxylic acids and ketones.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr data-path-to-node=\"14\"\u003e\n\u003ch3 data-path-to-node=\"15\"\u003eUnit 6: Amines\u003c\/h3\u003e\n\u003cul data-path-to-node=\"16\"\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"16,0,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"16,0,0\"\u003eBasicity and Synthesis:\u003c\/b\u003e Comparing the basicity of alkyl amines vs. aryl amines (aniline).\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"16,1,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"16,1,0\"\u003eReactions:\u003c\/b\u003e The Hofmann Elimination and the synthesis of diazonium salts (the \"gateway\" to many substituted benzenes).\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-path-to-node=\"17\"\u003eUnit 7: Biomolecules\u003c\/h3\u003e\n\u003cul data-path-to-node=\"18\"\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"18,0,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"18,0,0\"\u003eCarbohydrates:\u003c\/b\u003e Fischer projections, Haworth structures, and the reactivity of sugars.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"18,1,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"18,1,0\"\u003eAmino Acids and Proteins:\u003c\/b\u003e Zwitterions, isoelectric points, and the peptide bond.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"18,2,0\"\u003e\u003cb data-index-in-node=\"0\" data-path-to-node=\"18,2,0\"\u003eLipids and Nucleic Acids:\u003c\/b\u003e Brief overview of fats, steroids, and the structure of DNA\/RNA.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Chemistry Tutoring","offers":[{"title":"Default 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