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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Dimethyl butynedioate undergoes a Diels-Alder reaction with (2E,4E)-2,4-hexadiene. Show the structure and stereochemistry of the product.

Predict the major product (s) from the addition of 1 equivalent of HX and show the mechanism for each reaction below.

Di-tert-butyl-1,3-butadiene does not undergo Diels-Alder reactions. Explain.
Would you expect allene, , to show a UV absorption in
the 200 to 400 nm range? Explain.
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?
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