Table of contents

1. A Review of General Chemistry5h 5m
2. Molecular Representations1h 14m
3. Acids and Bases2h 46m
4. Alkanes and Cycloalkanes4h 17m
5. Chirality3h 39m
6. Thermodynamics and Kinetics1h 22m
7. Substitution Reactions1h 48m
8. Elimination Reactions2h 30m
9. Alkenes and Alkynes2h 9m
10. Addition Reactions3h 19m
11. Radical Reactions1h 58m
12. Alcohols, Ethers, Epoxides and Thiols2h 42m
13. Alcohols and Carbonyl Compounds2h 17m
14. Synthetic Techniques1h 26m
15. Analytical Techniques:IR, NMR, Mass Spect7h 3m
16. Conjugated Systems6h 13m
17. Ultraviolet Spectroscopy51m
18. Aromaticity2h 34m
19. Reactions of Aromatics: EAS and Beyond5h 1m
20. Phenols55m
21. Aldehydes and Ketones: Nucleophilic Addition4h 56m
22. Carboxylic Acid Derivatives: NAS2h 51m
23. The Chemistry of Thioesters, Phophate Ester and Phosphate Anhydrides1h 10m
24. Enolate Chemistry: Reactions at the Alpha-Carbon1h 53m
25. Condensation Chemistry2h 9m
26. Amines1h 43m
27. Heterocycles2h 0m
28. Carbohydrates5h 53m
29. Amino Acids4h 20m
30. Peptides and Proteins2h 42m
31. Catalysis in Organic Reactions1h 30m
32. Lipids 2h 50m
33. The Organic Chemistry of Metabolic Pathways2h 52m
34. Nucleic Acids1h 32m
35. Transition Metals6h 14m
36. Synthetic Polymers1h 49m

3. Acids and Bases

Acids and Bases

Organic Chemistry

3. Acids and Bases

Acids and Bases

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Multiple Choice

Which of the following is not a factor affecting the acidity of a compound?

Electronegativity of the atom bonded to hydrogen

Resonance stabilization of the conjugate base

Inductive effect from nearby electronegative atoms

Presence of a catalyst

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Verified step by step guidance

Understand that acidity in organic compounds is influenced by several factors that stabilize the conjugate base after the loss of a proton (H⁺).

Recognize that the electronegativity of the atom bonded to hydrogen affects acidity because more electronegative atoms can better stabilize the negative charge on the conjugate base.

Consider resonance stabilization, which allows the negative charge of the conjugate base to be delocalized over multiple atoms, increasing stability and thus acidity.

Examine the inductive effect, where nearby electronegative atoms can pull electron density away from the conjugate base, stabilizing it and increasing acidity.

Identify that the presence of a catalyst does not directly affect the intrinsic acidity of a compound, as catalysts typically influence the rate of reaction rather than the equilibrium position or stability of the conjugate base.