Exam 1: Introduction and Review
Exam 1: Introduction and Review127 Questions
Exam 2: Structure and Properties of Organic Molecules129 Questions
Exam 3: Structure and Stereochemistry of Alkanes129 Questions
Exam 4: The Study of Chemical Reactions128 Questions
Exam 5: Stereochemistry128 Questions
Exam 6: Alkyl Halides: Nucleophilic Substitution and Elimination132 Questions
Exam 7: Structure and Synthesis of Alkenes128 Questions
Exam 8: Reactions of Alkenes132 Questions
Exam 9: Alkynes124 Questions
Exam 10: Structure and Synthesis of Alcohols132 Questions
Exam 11: Reactions of Alcohols124 Questions
Exam 12: Infrared Spectroscopy and Mass Spectrometry120 Questions
Exam 13: Nuclear Magnetic Resonance Spectroscopy130 Questions
Exam 14: Ethers, Epoxides, and Thioethers127 Questions
Exam 15: Conjugated Systems, Orbital Symmetry, and Ultraviolet Spectroscopy130 Questions
Exam 16: Aromatic Compounds128 Questions
Exam 17: Reactions of Aromatic Compounds129 Questions
Exam 18: Ketones and Aldehydes132 Questions
Exam 19: Amines129 Questions
Exam 20: Carboxylic Acids125 Questions
Exam 21: Carboxylic Acid Derivatives128 Questions
Exam 22: Condensations and Alpha Substitutions of Carboxyl Compounds125 Questions
Exam 23: Carbohydrates and Nucleic Acids125 Questions
Exam 24: Amino Acids, Peptides, and Proteins127 Questions
Exam 25: Lipids127 Questions
Exam 26: Synthetic Polymers128 Questions
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Consider the set of compounds, NH3, HF, and H2O. Rank these compounds in order of increasing acidity and discuss your rationale.
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Use the curved arrow formalism to indicate the movement of electron pairs in the following reaction. 

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Add the appropriate formal charge to each atom in the molecule below. It is not necessary to indicate formal charges when zero. 

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Strong bases usually contain positively charged atoms of high electronegativity and no resonance stabilization.
(True/False)
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Add the appropriate formal charge to each atom in the molecule below. It is not necessary to indicate formal charges when zero. 

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Methanesulfonic acid, CH3SO3H, has a pKa of -7 while ethanol, CH3CH2OH, has a pKa of 15.9. Which is the stronger acid and what accounts for this large difference in relative acidity?
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A node is a region of high electron density between the two atoms in a covalent bond.
(True/False)
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Provide the Lewis structure of the conjugate acid of ethanol (CH3CH2OH).
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The Ka of formic acid is 1.7 x 10-4. The pKa of formic acid is ________.
(Multiple Choice)
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Draw the complete Lewis structure for the compound whose condensed formula is (CH3)2CHCHO.
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Calculate the pH of a 250 mL aqueous solution which contains 0.70 g of HCl.
(Short Answer)
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Which is more acidic, methanesulfonic acid (CH3SO3H) or propanoic acid (CH3CH2CO2H)? Explain.
(Essay)
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Draw a complete Lewis structure, including lone pairs, for (CH3)2CHCO2H.
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Which sequence correctly ranks the following protons in order of increasing acidity? 

(Multiple Choice)
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Calculate the molecular formula for the organic compound whose quantitative elemental analysis showed 48.6% caron and 8.1% hydrogen by weight.
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