Question

Consider the reaction of 2,2,4,4-tetramethylpentane with chlorine in light. The first step is initiation in the presence of light. $Cl-Cl \longrightarrow Cl \cdot + \cdot Cl$ Add curved arrows to show the mechanism of the propagation steps to form each monochlorination product shown. a) Formation of the 1-chloro-2,2,4,4-tetramethylpentane. $H-Cl$ $:Cl \cdot + H-CH_2 \longrightarrow \cdot CH_2 + :Cl-Cl \longrightarrow H_3C-CH_3$ $H_3C-CH_3$ $CH_3$ $CH_3$ $CH_3$ $CH_3$ $H_3C-CH_3$ $CH_3$ $CH_3$ $CH_3$ $CH_3$ Answer Bank

          Consider the reaction of 2,2,4,4-tetramethylpentane with chlorine in light.
The first step is initiation in the presence of light.
$Cl-Cl \longrightarrow Cl \cdot + \cdot Cl$
Add curved arrows to show the mechanism of the propagation steps to form each monochlorination product shown.
a) Formation of the 1-chloro-2,2,4,4-tetramethylpentane.
$H-Cl$
$:Cl \cdot + H-CH_2 \longrightarrow \cdot CH_2 + :Cl-Cl \longrightarrow H_3C-CH_3$
$H_3C-CH_3$
$CH_3$
$CH_3$
$CH_3$
$CH_3$
$H_3C-CH_3$
$CH_3$
$CH_3$
$CH_3$
$CH_3$
Answer Bank

consider the reaction of 2244 tetramethylpentane with chlorine in light the first step is initiation in the presence of light cl cl longrightarrow cl cdot cdot cl add curved arrows to show t 19863

Added by Beth M.

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