Chapter 14: 25Ec (page 447)
Give IUPAC names for the following compounds:
Short Answer
Hepta-2,3,5-triene
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Chapter 14: 25Ec (page 447)
Give IUPAC names for the following compounds:
Hepta-2,3,5-triene
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Propose a structure for a conjugated diene that gives the same product from both 1,2 and 1,4-addition of HBr.
Show the product of the Diels–Alder reaction of the following dienewith 3-buten-2-one, H2C=CHCOCH3. Make sure you show the fullstereochemistry of the reaction product.

Draw a segment of the polymer that might be prepared from 2-phenyl-1,3-butadiene.
Treatment of 3,4-dibromohexane with strong base leads to loss of2 equivalents of HBr and formation of a product with formula C6H10.Three products are possible. Name each of the three, and tell how youwould use 1H and 13C NMR spectroscopy to help identify them. Howwould you use UV spectroscopy?
Hydrocarbon A, , has a UV absorption at =236nm and gives hydrocarbon B, C10H18, on catalytic hydrogenation. Ozonolysis of A, followed by zinc/acetic acid treatment, yields the following diketo dialdehyde:

a)Propose two possible structures for A.
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