6. 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 obscrved compound after treating compound I with cyanide. :CEN : CN CI -CN II observed not observed a. Pruvide a detailed, stepwise mechanism for the transformation above that accounts livr the formation of pruduct II. Use the curved arIow lurmalism to show the tlow of electroLs. Show all lone pairs, intermediates, formul charges, und pertinent resonance structures.

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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A Aa Ao
AaßbCcDd AaBbCcDd AaBbCc AaBbCcD AaB
& Re
A
== Ev vv
1 Normal
1 Heading 2
1 No Spac. Heading 1
Title
A Se
Paragreph
Styles
Editi
6. 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 obscrved compound after
treating compound I with cyanide.
:CEN :
CN
CI
CN
observed
not observed
a. Provide a detailed, stepwise mechanism for the transformation above that accounts lir the
formation of pruduct II. Use the curved arrow lurmalism to show the tlow of clectroLs. Shew
all lene pairs, intermediates, formul charges, und pertinent resonance structures.
rited States
l n Fa Accesibility: Inwestigate
lext Predictinrs: O
D' Fucus
99+
**
F10
F11
PrtSc
F12
%23
3
4.
8
E
T.
Y
G
H
J
K
C
M
Alt
Ctri
V
N
Transcribed Image Text:Organic Chem 1 Week 5 Lab- Student.docx - Saved to this PC - P Search shiku sign Layout References Mailings Review View Developer Help OFir A Aa Ao AaßbCcDd AaBbCcDd AaBbCc AaBbCcD AaB & Re A == Ev vv 1 Normal 1 Heading 2 1 No Spac. Heading 1 Title A Se Paragreph Styles Editi 6. 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 obscrved compound after treating compound I with cyanide. :CEN : CN CI CN observed not observed a. Provide a detailed, stepwise mechanism for the transformation above that accounts lir the formation of pruduct II. Use the curved arrow lurmalism to show the tlow of clectroLs. Shew all lene pairs, intermediates, formul charges, und pertinent resonance structures. rited States l n Fa Accesibility: Inwestigate lext Predictinrs: O D' Fucus 99+ ** F10 F11 PrtSc F12 %23 3 4. 8 E T. Y G H J K C M Alt Ctri V N
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