organic chemistry midterm exam 1 study guide - information to memorize

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pKa Values Acids - The smaller the value of the pKa the more acidic the acid (stronger acid) - The more Acidic an acid is the more stable its conjugate base. - The less Acidic an acid is the less stable its conjugate base. - A more stable base (a weaker base) has a more acidic conjugate acid relative to a less stable base. n Name Formula 1 Methane CH 4 2 Ethane CH 3 CH 3 3 Propane CH 3 CH 2 CH 3 4 Butane CH 3 CH 2 CH 2 CH 3 5 Pentane CH 3 (CH 2 ) 3 CH 3 6 Hexane CH 3 (CH 2 ) 4 CH 3 7 Heptane CH 3 (CH 2 ) 5 CH 3 8 Octane CH 3 (CH 2 ) 6 CH 3 9 Nonane CH 3 (CH 2 ) 7 CH 3 10 Decane CH 3 (CH 2 ) 8 CH 3 11 Undecane CH 3 (CH 2 ) 9 CH 3 12 Dodecane CH 3 (CH 2 ) 10 CH 3 13 Tridecane CH 3 (CH 2 ) 11 CH 3 14 Tetradecane CH 3 (CH 2 ) 12 CH 3 15 Pentadecane CH 3 (CH 2 ) 13 CH 3 16 Hexadecane CH 3 (CH 2 ) 14 CH 3 17 Heptadecane CH 3 (CH 2 ) 15 CH 3 18 Octadecane CH 3 (CH 2 ) 16 CH 3 19 Nonadecane CH 3 (CH 2 ) 17 CH 3 20 Icosane CH 3 (CH 2 ) 18 CH 3

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Organic Chemistry Midterm Exam 1 Study Guide - Information to Memorize1. Acidity Trends- pKa- Acid Strength- Base Strength- Conjugate Base Stability2. Conjugate Acids & Conjugate Bases3. Names, Structures & pKa Values ofA) HalogensB) Inorganic Acids - Strong Acids - Weak AcidsC) Organic Acids - Oxyacid - Carbon Acids3. Common Functional Groups (Alcohols, Ethers, Thiols, Alkenes, Alkynes, …) - Common Names - Classes - Structure - Examples 4. Alkane Prefixes: Names & Formulas5. Primary, Secondary & Tertiary Carbons and Hydrogens6. Branched Alkyl Groups- Structures- Common Names- Examples- Systematic Names- Types of Carbon Bonds7. Periodic Trends- Atomic radii- Ionization E- Electron affinity- Electronegativity8. Halogenation F2, Cl2, Br2 & I2- Initiation Steps- Propagation Steps- Termination Steps

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Page 1: Organic Chemistry Midterm Exam 1 Study Guide - Information to Memorize

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pKa Values Acids - The smaller the value of the pKa the more acidic the acid (stronger acid) - The more Acidic an acid is the more stable its conjugate base. - The less Acidic an acid is the less stable its conjugate base. - A more stable base (a weaker base) has a more acidic conjugate acid relative to a less stable base. !

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n Name Formula 1 Methane CH4 2 Ethane CH3CH3 3 Propane CH3CH2CH3 4 Butane CH3CH2CH2CH3 5 Pentane CH3(CH2)3CH3 6 Hexane CH3(CH2)4CH3 7 Heptane CH3(CH2)5CH3 8 Octane CH3(CH2)6CH3 9 Nonane CH3(CH2)7CH3 10 Decane CH3(CH2)8CH3 11 Undecane CH3(CH2)9CH3 12 Dodecane CH3(CH2)10CH3 13 Tridecane CH3(CH2)11CH3 14 Tetradecane CH3(CH2)12CH3 15 Pentadecane CH3(CH2)13CH3 16 Hexadecane CH3(CH2)14CH3 17 Heptadecane CH3(CH2)15CH3 18 Octadecane CH3(CH2)16CH3 19 Nonadecane CH3(CH2)17CH3 20 Icosane CH3(CH2)18CH3

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Page 2: Organic Chemistry Midterm Exam 1 Study Guide - Information to Memorize

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