Chapter 15: Q 13P (page 770)
Show how you might synthesize the following compounds starting with bromobenzene, and alkyl or alkenyl halides of four carbon atoms or fewer.
a. 3-phenylprop-1-ene
b.5-methylhex-2-ene
c. dec-5-ene
Short Answer
a)

b)

c)

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Chapter 15: Q 13P (page 770)
Show how you might synthesize the following compounds starting with bromobenzene, and alkyl or alkenyl halides of four carbon atoms or fewer.
a. 3-phenylprop-1-ene
b.5-methylhex-2-ene
c. dec-5-ene
a)

b)

c)

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What dienes and dienophiles would react to give the following Diels-Alder products?
a)

b)

c)

d)

e)

f)

Phenolphthalein is an acid-base indicator that is colorless below pH 8 and red above pH 8. Explain briefly why the first structure is colorless and the second structure is colored.

Question: When 3-bromo-1-methylcyclohexene undergoes solvolysis in hot ethanol, two products are formed. Propose a mechanism that accounts for both of these products.

Question: Predict the product(s) of light-initiated reaction with NBS in CCl4 for the following starting materials.

Question: When N-bromosuccinimide is added to hex-1-ene in and a sunlamp is shone on the mixture, three products result.
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