Chapter 9: Q17E (page 263)
The following cycloalkyne is too unstable to exist. Explain
Short Answer
The linear geometry is distorted in the cyclopentyne and so the molecule is unstable.
Chapter 9: Q17E (page 263)
The following cycloalkyne is too unstable to exist. Explain
The linear geometry is distorted in the cyclopentyne and so the molecule is unstable.
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Get started for free1-Octen-3-ol, a potent mosquito attractant commonly used in mosquito traps, can be prepared in two steps from hexanal, . The first step is an acetylide-addition reaction like that described in Problem 9-50. What is the structure of the product from the first step, and how can it be converted into 1-octen-3-ol?
The pkaof acetone, CH3COCH3, is 19.3. Which of the following bases is strong enough to deprotonate acetone?
(b)
Arrange the carbocations below in order of increasing stability.
Synthesize the following compounds using 1-butyne as the only source of carbon along with any inorganic reagents you need. More than one step may be needed.(a) 1,1,2,2- Tetrachlorobutane(b) 1,1- Dichloro-2-ethylcyclopropane
Which of the following bases could be used to deprotonate 1-butyne?
(a)
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