Chapter 10: Q10-25E-b (page 308)
How would you prepare the following compounds, starting with cyclopentene and any other reagents needed? (b) Methylcyclopentane.
Short Answer
Methylcyclopentane can be formed in the following way:
Chapter 10: Q10-25E-b (page 308)
How would you prepare the following compounds, starting with cyclopentene and any other reagents needed? (b) Methylcyclopentane.
Methylcyclopentane can be formed in the following way:
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and have isolated (in low yield) . How many stereoisomers of the product are formed, and in what ratio? Are any of the isomers optically active? (See Problem 10-38.)
Question: How might you replace a halogen substituent by a deuterium atom if you wanted to prepare a deuterated compound?
How would you prepare the following compounds, starting with cyclopentene and any other reagents needed? (e) Cyclopentylcyclopentane.
Give IUPAC names for the following alkyl halide (a):
(a)
Taking the relative reactivities of 1°, 2°, and 3° hydrogen atoms into account, what product(s) would you expect to obtain from monochlorination of 2-methylbutane? What would the approximate percentage of each product be? (Don’t forget to take into account the number of each kind of hydrogen.)
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