{"product_id":"organic-chemistry-1-10-sessions","title":"Organic Chemistry 1 - 10 sessions","description":"\u003ch2 data-path-to-node=\"0\"\u003eOrganic Chemistry 1 Syllabus\u003c\/h2\u003e\n\u003cp data-path-to-node=\"1\"\u003eOrganic Chemistry 1 focuses on the structure, properties, and reactivity of carbon-based molecules. It shifts away from the heavy calculations of General Chemistry and emphasizes 3D visualization, patterns of reactivity, and the \"mechanisms\" of how bonds break and form.\u003c\/p\u003e\n\u003chr data-path-to-node=\"2\"\u003e\n\u003ch3 data-path-to-node=\"3\"\u003eUnit 1: Structure, Bonding, and Acids\/Bases\u003c\/h3\u003e\n\u003cul data-path-to-node=\"4\"\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"4,0,0\"\u003e\u003cb data-path-to-node=\"4,0,0\" data-index-in-node=\"0\"\u003eAtomic Orbitals:\u003c\/b\u003e Review of \u003cspan class=\"math-inline\" data-math=\"sp^3\" data-index-in-node=\"27\"\u003esp3\u003c\/span\u003e, \u003cspan class=\"math-inline\" data-math=\"sp^2\" data-index-in-node=\"33\"\u003esp2\u003c\/span\u003e, and \u003cspan class=\"math-inline\" data-math=\"sp\" data-index-in-node=\"43\"\u003esp\u003c\/span\u003e hybridization and molecular geometry.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"4,1,0\"\u003e\u003cb data-path-to-node=\"4,1,0\" data-index-in-node=\"0\"\u003eResonance:\u003c\/b\u003e Drawing and evaluating the stability of resonance contributors.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"4,2,0\"\u003e\u003cb data-path-to-node=\"4,2,0\" data-index-in-node=\"0\"\u003eOrganic Acids and Bases:\u003c\/b\u003e Using \u003cspan class=\"math-inline\" data-math=\"pK_a\" data-index-in-node=\"31\"\u003epKa\u003c\/span\u003e values to predict the direction of equilibrium and understanding how structure affects acidity.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-path-to-node=\"5\"\u003eUnit 2: Alkanes and Cycloalkanes\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-path-to-node=\"6,0,0\" data-index-in-node=\"0\"\u003eNomenclature:\u003c\/b\u003e Mastering the IUPAC system for naming complex organic chains.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"6,1,0\"\u003e\u003cb data-path-to-node=\"6,1,0\" data-index-in-node=\"0\"\u003eConformational Analysis:\u003c\/b\u003e Using Newman projections to analyze rotation around carbon-carbon bonds (staggered vs. eclipsed).\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"6,2,0\"\u003e\u003cb data-path-to-node=\"6,2,0\" data-index-in-node=\"0\"\u003eRing Strain:\u003c\/b\u003e Understanding the stability of cycloalkanes and the \"chair\" conformation of cyclohexane.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-path-to-node=\"7\"\u003eUnit 3: Stereochemistry\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-path-to-node=\"8,0,0\" data-index-in-node=\"0\"\u003eChirality:\u003c\/b\u003e Identifying chiral centers and molecules that are mirror images (enantiomers).\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"8,1,0\"\u003e\u003cb data-path-to-node=\"8,1,0\" data-index-in-node=\"0\"\u003eR\/S Configuration:\u003c\/b\u003e Applying priority rules to label the 3D orientation of atoms.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"8,2,0\"\u003e\u003cb data-path-to-node=\"8,2,0\" data-index-in-node=\"0\"\u003eDiastereomers and Meso Compounds:\u003c\/b\u003e Understanding molecules with multiple chiral centers.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-path-to-node=\"9\"\u003eUnit 4: Substitution and Elimination Reactions\u003c\/h3\u003e\n\u003cul data-path-to-node=\"10\"\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"10,0,0\"\u003e\u003cb data-path-to-node=\"10,0,0\" data-index-in-node=\"0\"\u003e\u003cspan class=\"math-inline\" data-math=\"S_N2\" data-index-in-node=\"0\"\u003eSN2\u003c\/span\u003e Reactions:\u003c\/b\u003e Bimolecular nucleophilic substitution (one-step, \"backside attack\").\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"10,1,0\"\u003e\u003cb data-path-to-node=\"10,1,0\" data-index-in-node=\"0\"\u003e\u003cspan class=\"math-inline\" data-math=\"S_N1\" data-index-in-node=\"0\"\u003eSN1\u003c\/span\u003e Reactions:\u003c\/b\u003e Unimolecular substitution involving a carbocation intermediate.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"10,2,0\"\u003e\u003cb data-path-to-node=\"10,2,0\" data-index-in-node=\"0\"\u003eElimination (\u003cspan class=\"math-inline\" data-math=\"E1\" data-index-in-node=\"13\"\u003eE1\u003c\/span\u003e and \u003cspan class=\"math-inline\" data-math=\"E2\" data-index-in-node=\"20\"\u003eE2\u003c\/span\u003e):\u003c\/b\u003e How bases remove atoms to create double bonds (alkenes).\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"10,3,0\"\u003e\u003cb data-path-to-node=\"10,3,0\" data-index-in-node=\"0\"\u003eRegioselectivity:\u003c\/b\u003e Predicting the major product using Zaitsev’s Rule.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-path-to-node=\"11\"\u003eUnit 5: Alkenes and Alkynes\u003c\/h3\u003e\n\u003cul data-path-to-node=\"12\"\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"12,0,0\"\u003e\u003cb data-path-to-node=\"12,0,0\" data-index-in-node=\"0\"\u003eAddition Reactions:\u003c\/b\u003e Adding \u003cspan class=\"math-inline\" data-math=\"H_2\" data-index-in-node=\"27\"\u003eH2\u003c\/span\u003e, \u003cspan class=\"math-inline\" data-math=\"X_2\" data-index-in-node=\"32\"\u003eX2\u003c\/span\u003e (halogens), and \u003cspan class=\"math-inline\" data-math=\"H_2O\" data-index-in-node=\"52\"\u003eH2O\u003c\/span\u003e across pi bonds.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"12,1,0\"\u003e\u003cb data-path-to-node=\"12,1,0\" data-index-in-node=\"0\"\u003eMarkovnikov’s Rule:\u003c\/b\u003e Predicting where substituents will add based on carbocation stability.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"12,2,0\"\u003e\u003cb data-path-to-node=\"12,2,0\" data-index-in-node=\"0\"\u003eOxidation and Reduction:\u003c\/b\u003e Hydroboration-oxidation, ozonolysis, and hydrogenation.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-path-to-node=\"13\"\u003eUnit 6: Alcohols, Ethers, and Epoxides\u003c\/h3\u003e\n\u003cul data-path-to-node=\"14\"\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"14,0,0\"\u003e\u003cb data-path-to-node=\"14,0,0\" data-index-in-node=\"0\"\u003eSynthesis:\u003c\/b\u003e Converting alkyl halides and alkenes into alcohols.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"14,1,0\"\u003e\u003cb data-path-to-node=\"14,1,0\" data-index-in-node=\"0\"\u003eReactivity:\u003c\/b\u003e Using alcohols as nucleophiles or converting them into better leaving groups (tosylates).\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"14,2,0\"\u003e\u003cb data-path-to-node=\"14,2,0\" data-index-in-node=\"0\"\u003eEpoxide Ring-Opening:\u003c\/b\u003e Analyzing how ring strain drives reactivity in cyclic ethers.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-path-to-node=\"15\"\u003eUnit 7: Spectroscopy and Structure Determination\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-path-to-node=\"16,0,0\" data-index-in-node=\"0\"\u003eInfrared (IR) Spectroscopy:\u003c\/b\u003e Using light to identify functional groups (like \u003cspan class=\"math-inline\" data-math=\"C=O\" data-index-in-node=\"76\"\u003eC=O\u003c\/span\u003e or \u003cspan class=\"math-inline\" data-math=\"O-H\" data-index-in-node=\"83\"\u003eO-H\u003c\/span\u003e bonds).\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"16,1,0\"\u003e\u003cb data-path-to-node=\"16,1,0\" data-index-in-node=\"0\"\u003eMass Spectrometry:\u003c\/b\u003e Determining molecular weight and fragmentation patterns.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp data-path-to-node=\"16,2,0\"\u003e\u003cb data-path-to-node=\"16,2,0\" data-index-in-node=\"0\"\u003eNuclear Magnetic Resonance (NMR):\u003c\/b\u003e Mapping the carbon-hydrogen framework of a molecule.\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Chemistry Tutoring","offers":[{"title":"Default Title","offer_id":44036774330465,"sku":null,"price":600.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0631\/8568\/2529\/files\/orgo1.jpg?v=1776472035","url":"https:\/\/chemistrytutor.us\/products\/organic-chemistry-1-10-sessions","provider":"Chemistry Tutoring","version":"1.0","type":"link"}