Chapter 14: 29E (page 447)
Propose a structure for a conjugated diene that gives the same product from both 1,2 and 1,4-addition of HBr.
Short Answer
Cyclopentadiene
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Chapter 14: 29E (page 447)
Propose a structure for a conjugated diene that gives the same product from both 1,2 and 1,4-addition of HBr.
Cyclopentadiene
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1,3-Cyclopentadiene polymerizes slowly at room temperature to yield
a polymer that has no double bonds except on the ends. On heating, the
polymer breaks down to regenerate 1,3-cyclopentadiene. Propose a structure for the product.
Electrophilic addition of to isoprene (2-methyl-1,3-butadiene) yields the following product mixture:
Of the 1,2-addition products, explain why 3,4-dibromo-3-methyl-1-butene (21%) predominates over 3,4-dibromo-2-methyl-1-butene (3%).
Which of the following dienes have an s-cis conformation, and which have an s-trans conformation? Of the s-trans dienes, which can readily rotate to s-cis?

The following ultraviolet absorption maxima have been measured:
1,3-Butadiene 217 nm
2-Methyl-1,3-butadiene 220 nm
1,3-Pentadiene 223 nm
2,3-Dimethyl-1,3-butadiene 226 nm
2,4-Hexadiene227 nm
2,4-Dimethyl-1,3-pentadiene 232 nm
2,5-Dimethyl-2,4-hexadiene 240 nm
What conclusion can you draw about the effect of alkyl substitution on
UV absorption maxima? Approximately what effect does each added
alkyl group have?
The following Diene does not undergo Diels–Alder reactions. Explain.

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