
Chemistry
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Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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How would you carry out each of the following transformations?

Transcribed Image Text:**Synthesis Using Alkenes**
**8-50** How would you carry out the following transformations? Tell what reagents you would use in each case.
(a) Cyclopentene to a diol:
- \( \text{Cyclopentene} \rightarrow \text{cis-1,2-cyclopentanediol} \)
(b) Cyclopentene to a cyclopentanol:
- \( \text{Cyclopentene} \rightarrow \text{cyclopentanol} \)
(c) Cyclopentene to a dichloride with retention of stereochemistry:
- \( \text{Cyclopentene} \rightarrow \text{cis-1,2-Dichlorocyclopentane} \)
(d) Cyclohexanol to a methylcyclohexene:
- \( \text{Cyclohexanol} \rightarrow \text{1-methylcyclohexene} \)
(e) 2-Butene to ketones:
- \( \text{CH}_3\text{CH=CHCH}_3 \rightarrow \text{CH}_3\text{CH}_2\text{COH (acetone)} + \text{CH}_3\text{CH}_2\text{COH} \)
(f) Propylene with alcohol to an ether:
- \( \text{CH}_3\text{C=CH}_2 + \text{CH}_3\text{CH}_2\text{OH} \rightarrow \text{a product} \)
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