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.

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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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Add curved arrows to the following polar reactions to indicate the flow of electrons in each:
(a)

(b)

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.

Identify the following reactions as additions, eliminations, substitutions, or rearrangements:
a.

b.

c.

d.

Draw all of the different monochlorinated products one would obtain by the radical chlorination of these compounds. (Do not consider the stereochemistry of the products in your answer.)

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