Question

Complete the multistep mechanism for the formation of each of the possible monochlorination products from reaction of 2,2,4,4-tetramethylpentane with chlorine in light.

Map Complete the multistep mechanism for the formation of each of the possible monochlorination products from reaction of 2,2,4,4-tetramethylpentane with chlorine in light. Initiation step in the presence of light. Use curved arrows to show the mechanism of the propagation steps below. (Click on the blue box to toggle through four possible arrow choices.) a) Formation of the 1-chloro-2,2,4,4-tetramethylpentane. 填. C-CH2 CH3 :Ci. CH2 CH3 H3 CH3 H3 H3 H3 ČH3 CH3 CH3 CH3

Answer 1

Complete the multistep mechanism for the formation of each of the possible monochlorination products from reaction of 2,2,4,4-tetramethylpentane with chlorine in light. Initiation step in the presence of light. Use curved arrows to show the mechanism of the propagation steps below. (Click on the blue box to toggle through four possible arrow choices.) a) Formation of the 1-chloro-2,2,4,4-tetramethylpentane C-CH2 CH3 :CI H2 CH3 H3 CH3 H3 H3 H3 ČH3 CH3 CH3 CH3 CH3 CH3

b) Formation of the 3-chloro-2,2,4,4-tetramethylpentane. CH3 CH3 CH3 На CH3 CH3 CH3 CH3 CH3 CH3 CH3 CH3