Exam 22: Amines
Exam 1: A Review of General Chemistry: Electrons, Bonds, and Molecular Properties191 Questions
Exam 2: Molecular Representations168 Questions
Exam 3: Acids and Bases127 Questions
Exam 4: Alkanes and Cycloalkanes116 Questions
Exam 5: Stereoisomerism141 Questions
Exam 6: Chemical Reactivity and Mechanisms96 Questions
Exam 7: Alkyl Halides: Nucleophilic Substitution and Elimination Reactions224 Questions
Exam 8: Addition Reactions of Alkenes153 Questions
Exam 9: Alkynes177 Questions
Exam 10: Radical Reactions102 Questions
Exam 11: Synthesis106 Questions
Exam 12: Alcohols and Phenols147 Questions
Exam 13: Ethers and Epoxides; Thiols and Sulfides139 Questions
Exam 14: Infrared Spectroscopy and Mass Spectrometry135 Questions
Exam 15: Nuclear Magnetic Resonance Spectroscopy140 Questions
Exam 16: Conjugated Pi Systems and Pericyclic Reactions140 Questions
Exam 17: Aromatic Compounds118 Questions
Exam 18: Aromatic Substitution Reactions122 Questions
Exam 19: Aldehydes and Ketones169 Questions
Exam 20: Carboxylic Acids and Their Derivatives144 Questions
Exam 21: Alpha Carbon Chemistry: Enols and Enolates147 Questions
Exam 22: Amines112 Questions
Exam 23: Introduction to Organometallic Compounds118 Questions
Exam 24: Carbohydrates144 Questions
Exam 25: Amino Acids, Peptides, and Proteins133 Questions
Exam 26: Lipids123 Questions
Exam 27: Synthetic Polymers119 Questions
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Provide the reagents necessary to carry out the following conversion. 
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Provide the reagents necessary to carry out the following conversion. 
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Provide the reagents necessary to carry out the following conversion. 
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A compound with molecular formula C8H19N exhibits a triplet at 0.9 (6H), a singlet at 1.1 (1H), a sextet at 1.3 (4H), a quintet at 1.4 (4H) and a triplet at 2.6 (4H) in its 1H NMR spectrum. Its IR spectrum shows a medium absorption band near 3400 cm-1. Its 13C NMR spectrum showed peaks at 13.7, 20.5, 30.4 and 49.2. What is the structure for this compound?
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A compound with molecular formula C8H10BrN exhibits a singlet at 1.2 (2H), a triplet at 2.8 (2H), a triplet at 3.0 (2H), a doublet at 7.1 (2H) and a doublet at 7.4 (2H) in its 1H NMR spectrum. Its IR spectrum shows two medium absorption bands near 3400 cm-1. What is the structure for this compound?
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Provide the reagents necessary to carry out the following conversion. 
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Pyridoxamine, aka vitamin B6, has the following structure. Which nitrogen is more basic? Explain your choice. 
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