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Exam 8: Alkenes: Structure and Preparation Via Elimination Reactions

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Exam 1: A Review of General Chemistry: Electrons, Bonds, and Molecular Properties86 Questionsadd course
Exam 2: Molecular Representations114 Questionsadd course
Exam 3: Acids and Bases72 Questionsadd course
Exam 4: Alkanes and Cycloalkanes66 Questionsadd course
Exam 5: Stereoisomerism94 Questionsadd course
Exam 6: Chemical Reactivity and Mechanisms86 Questionsadd course
Exam 7: Substitution Reactions103 Questionsadd course
Exam 8: Alkenes: Structure and Preparation Via Elimination Reactions76 Questionsadd course
Exam 9: Addition Reactions of Alkenes40 Questionsadd course
Exam 10: Alkynes161 Questionsadd course
Exam 11: Radical Reactions52 Questionsadd course
Exam 12: Synthesis55 Questionsadd course
Exam 13: Alcohols and Phenols71 Questionsadd course
Exam 14: Ethers and Epoxides; Thiols and Sulfides102 Questionsadd course
Exam 16: Nuclear Magnetic Resonance Spectroscopy90 Questionsadd course
Exam 15: Infrared Spectroscopy and Mass Spectrometry108 Questionsadd course
Exam 17: Conjugated Pi Systems and Pericyclic Reactions45 Questionsadd course
Exam 18: Aromatic Compounds79 Questionsadd course
Exam 19: Aromatic Substitution Reactions64 Questionsadd course
Exam 20: Aldehydes and Ketones97 Questionsadd course
Exam 21: Carboxylic Acids and Their Derivatives58 Questionsadd course
Exam 22: Alpha Carbon Chemistry: Enols and Enolates89 Questionsadd course
Exam 23: Amines65 Questionsadd course
Exam 24: Carbohydrates101 Questionsadd course
Exam 25: Amino Acids, Peptides, and Proteins99 Questionsadd course
Exam 26: Lipids82 Questionsadd course
Exam 27: Synthetic Polymers85 Questionsadd course
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Show the mechanism for the following elimination,assuming that it is a concerted reaction. Show the mechanism for the following elimination,assuming that it is a concerted reaction.

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Question 61

Draw the structure of 3-methylcyclopentene.

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Question 62

Will the following alcohol be likely to undergo rearrangement during a dehydration reaction? Will the following alcohol be likely to undergo rearrangement during a dehydration reaction?

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Question 63

Show the mechanism for the following elimination,assuming that it is a stepwise reaction. Show the mechanism for the following elimination,assuming that it is a stepwise reaction.

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Question 64

Draw the isomer of 2-bromo-1,1,3-trimethylcyclohexane that would be more reactive in an E2 elimination.

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Question 65

Draw the major product of the following reaction. Draw the major product of the following reaction.

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Question 66

Draw the E isomer of 3,4-dimethyl-3-hexene.

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Question 67

Which of the following is the correct IUPAC name for the following compound? Which of the following is the correct IUPAC name for the following compound?

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Question 68

Provide an IUPAC name for the following compound. Provide an IUPAC name for the following compound.

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Question 69

Provide an IUPAC name for the following compound. Provide an IUPAC name for the following compound.

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Question 70

Provide an IUPAC name for the following compound. Provide an IUPAC name for the following compound.

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Question 71

By what mechanism is the following reaction likely to occur? By what mechanism is the following reaction likely to occur?

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Question 72

What is the product of the following elimination? What is the product of the following elimination?

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Question 73

Show the mechanism for the following elimination,assuming that it is a stepwise reaction. Show the mechanism for the following elimination,assuming that it is a stepwise reaction.

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Question 74

Provide an IUPAC name for the following compound. Provide an IUPAC name for the following compound.

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Question 75

What is the structure of the rearranged carbocation in the following dehydration? What is the structure of the rearranged carbocation in the following dehydration?

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Question 76
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