11. In an organic chemistry lab, chemists were attempting to convert compound I into compound III via a substitution reaction. To their surprise, compound II was the only observed compound after treating compound I with cyanide. :CEN : CI CN II not observed observed a. Provide a detailed, stepwise mechanism for the transformation above that accounts for the formation of product II. Use the curved arrows to show the flow of electrons. Show all lone pairs, intermediates, formal charges, and pertinent resonance structures.

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also answer y product 2 is formed instead of product 3

11. In an organic chemistry lab, chemists were attempting to convert compound I into compound II
via a substitution reaction. To their surprise, compound II was the only observed compound after
treating compound I with cyanide.
:CEN :
CN
-CI
CN
II
not observed
observed
Provide a detailed, stepwise mechanism for the transformation above that accounts for the
formation of product II. Use the curved arrows to show the flow of electrons.. Show all lone
pairs, intermediates, formal charges, and pertinent resonance structures.
a.
Transcribed Image Text:11. In an organic chemistry lab, chemists were attempting to convert compound I into compound II via a substitution reaction. To their surprise, compound II was the only observed compound after treating compound I with cyanide. :CEN : CN -CI CN II not observed observed Provide a detailed, stepwise mechanism for the transformation above that accounts for the formation of product II. Use the curved arrows to show the flow of electrons.. Show all lone pairs, intermediates, formal charges, and pertinent resonance structures. a.
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