Chapter 14: 25Eb (page 447)
Give IUPAC names for the following compounds:
Short Answer
Hepta-1,3,5-triene
Chapter 14: 25Eb (page 447)
Give IUPAC names for the following compounds:
Hepta-1,3,5-triene
All the tools & learning materials you need for study success - in one app.
Get started for freeDraw the resonance forms that result when the dienes below are protonated. If the resonance forms differ in energy, identify the most stableone.
a)
b)
c)
Aldrin, a chlorinated insecticide now banned from use in the United
States, can be made by Diels–Alder reaction of hexachloro-1,3-cyclopentadienewith norbornadiene. What is the structure of aldrin?
Would you expect a conjugated diyne such as 1,3-butadiyne to undergo Diels-Alder reaction with a dienophile? Explain.
How could you use Diels-Alder reactions to prepare the following products ? Show the starting diene and dienophile in each case.
c)
Addition of HCl to 1-methoxycyclohexene yields 1-chloro-1-methoxycyclohexane as a sole product. Use resonance structures to explain whynone of the other regioisomer is formed.
What do you think about this solution?
We value your feedback to improve our textbook solutions.