Exam 7: Alkenes and Alkynes I: Properties and Synthesis, Elimination Reactions of Alkyl Halides
Exam 1: Carbon Compounds and Chemical Bonds134 Questions
Exam 2: Representative Carbon Compounds: Functional Groups, Intermolecular Forces, and Infrared Ir Spectroscopy114 Questions
Exam 3: An Introduction to Organic Reactions: Acids and Bases47 Questions
Exam 4: Alkanes: Nomenclature, Conformational Analysis, and an Introduction to Synthesis125 Questions
Exam 5: Stereochemistry: Chiral Molecules150 Questions
Exam 6: Ionic Reactions - Nucleophilic Substitution and Elimination Reactions of Alkyl Halides146 Questions
Exam 7: Alkenes and Alkynes I: Properties and Synthesis, Elimination Reactions of Alkyl Halides99 Questions
Exam 8: Alkenes and Alkynes Ii: Addition Reactions140 Questions
Exam 9: Nuclear Magnetic Resonance and Mass Spectrometry: Tools for Structure Determination94 Questions
Exam 10: Radical Reactions114 Questions
Exam 11: Alcohols and Ethers172 Questions
Exam 12: Alcohols From Carbonyl Compounds Oxidation-Reduction and Organometallic Compounds147 Questions
Exam 13: Conjugated Unsaturated Systems166 Questions
Exam 14: Aromatic Compounds151 Questions
Exam 15: Reactions of Aromatic Compounds173 Questions
Exam 16: Aldehydes and Ketones I Nucleophilic Addition to the Carbonyl Group165 Questions
Exam 17: Aldehydes and Ketones Ii Aldol Reactions131 Questions
Exam 18: Carboxylic Acids and Their Derivatives Nucleophilic Addition - Elimination at the Acyl Carbon124 Questions
Exam 19: Synthesis and Reactions of Beta-Dicarbonyl Compounds: More Chemistry of Enolate Ions131 Questions
Exam 20: Amines148 Questions
Exam 21: Phenols and Aryl Halides: Nucleophilic Aromatic Substitution87 Questions
Exam 22: Carbohydrates104 Questions
Exam 23: Lipids99 Questions
Exam 24: Amino Acids and Proteins94 Questions
Exam 25: Nucleic Acids and Protein Synthesis89 Questions
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What "new",more stable,carbocation(s)may be formed when the following carbocation undergoes spontaneous rearrangement? 

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Draw the structures of all stereoisomers of 2-chloro-4-methyl-3-hexene,clearly showing all stereochemical details,using appropriate 3-D representations (dash-wedge,etc. )as relevant.
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Which mechanistic step in the acid-catalyzed dehydration of 3,3-dimethyl-2-butanol is the rate determining step?
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What is the major product of the reaction of the following reaction? 

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Which would be the major product of the following reaction sequence? 

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What is the major product for the following reaction sequence? 

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The IR spectrum of an unknown substance Q,C9H16,is found to have distinct peaks at 3310 cm-1 and 2140 cm-1.Treatment of Q with excess H2 in presence of Raney Ni affords nearly quantitative yields of 2,3-dimethylheptane.Propose a reasonable structure for Q,based on the above information,briefly explaining your rationale.Also give its IUPAC name.
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A compound,C6H10,which reacts with 2 mol of hydrogen over a platinum catalyst and which shows an IR absorption band at approximately 3300 cm-1 could be: 

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Which product (or products)would be formed in appreciable amount(s)when trans-1-bromo-2-methylcyclohexane undergoes dehydrohalogenation upon treatment with sodium ethoxide in ethanol? 

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What is the major product for the following reaction sequence? 

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Which reaction would not result in alkylation of the acetylide anion?
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Which of the following methods could be used to synthesize 4,4-dimethyl-2-hexyne?
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On hydrogenation,a compound C9H12 absorbs 2 mol of hydrogen.Which of the following is a possible structure for the compound? 

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