Chapter 10: Q10-8P-d. (page 298)
Question: How would you prepare the following alkyl halides from the corresponding alcohols?

Short Answer
Answer
The given compound is 1-fluoro,3,3-dimethylcyclopentane. It can be prepared as the following way:

Chapter 10: Q10-8P-d. (page 298)
Question: How would you prepare the following alkyl halides from the corresponding alcohols?

Answer
The given compound is 1-fluoro,3,3-dimethylcyclopentane. It can be prepared as the following way:

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Draw structures corresponding to the following IUPAC names: (a) 2,3-Dichloro-4-methylhexane.
Predict the product and provide the entire catalytic cycle for theSuzuki–Miyaura reactions below.

Question: How strong a base would you expect a Grignard reagent to be? Look at Table 9-1 on page 276, and predict whether the following reactions will occur as written. (The of is 35.)

The major product of the reaction of methylenecyclohexane with N-bromosuccinimide is 1-(bromomethyl)cyclohexene. Explain.

Question: The syntheses shown here are unlikely to occur as written. What is
wrong with each?

Reaction 1

Reaction 2

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