Chapter 6: Q27E (page 181)
Draw the electron-pushing mechanism for each radical reaction below. Identify each step as initiation, propagation, or termination.
(a)
b)
c)
Short Answer
a.
b.
c.
Chapter 6: Q27E (page 181)
Draw the electron-pushing mechanism for each radical reaction below. Identify each step as initiation, propagation, or termination.
(a)
b)
c)
a.
b.
c.
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Get started for freeRadical chlorination of pentane is a poor way to prepare 1-chloropentane, but radical chlorination of neopentane,, is a good way to prepare neopentyl chloride,. Explain.
Draw the more stable chair conformation of the following molecules, and estimate the amount of strain in each:
2-Chloro-2-methylpropane reacts with water in three steps to yield 2-methyl-2-propanol. The first step is slower than the second, which in turn is much slower than the third. The reaction takes place slowly at room temperature, and the equilibrium constant is approximately 1.
Identify the following reactions as additions, eliminations, substitutions, or rearrangements:
a.
b.
c.
d.
Electrostatic potential maps of (a) formaldehyde and (b) methanethiol are shown. Is the formaldehyde carbon atom likely to be electrophilic or nucleophilic? What about the methanethiol sulfur atom? Explain.
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