9. The four compounds listed below undergo SN1 reactions at increasingly faster rates. Foreach compound, provide the contributing resonance forms for the carbocation intermediatethat would be formed. Explain why the resonance forms provide information about the ratedifferences.Brelooesnsibto0 018-terl (V-) woled bewBrTIIỌCH3VIBrefin 8 to muloage AMA H ar ni ese of oaqe uoy bluow 6uleot iedW 8Snoltone gaiwollot erl of18Broubog toom)(blsitrwob) blall wol ta anoloiq olemots yino ed bluow enerfT AJolduch.a.ed.bluow.nodhsa.ailysad ad no anotong onl tot leipie enT 8Jolght s od bluaw anoioiq lytom er tot lenpie erdTJolduob s ed bluow anotoanegotbyd S yino not olsigatni bhiow anolong lydlam arl hol langiae enT3

SN1 is a nucleophilic substitution reaction. In this reaction formation of intermediate…

9. The four compounds listed below undergo SN1 reactions at increasingly faster rates. For each compound, provide the contributing resonance forms for the carbocation intermediate that would be formed. Explain why the resonance forms provide information about the rate differences. Br 618 oted Br II OCH3 VI Br ofis 8 lo mubage AMA H er niese of lbeqe uoy bluow euleot edW8 Snollose gaiwollot eri ot Br oubog toa (blsitmwob) blell wol te anolog ollamots Aylno ed bluow enerT A Jelduch.a.ed.bluownodhaa.ailsnad a no anotog on tot lepie erT 8 Jolght s od bluow anoioig tom sr ot lenpie erTO olduob s ed bluow and aneporbyd S yino 1ot alsgatni bhow enotong lydlem arl hol lannie erf

9. The four compounds listed below undergo SN1 reactions at increasingly faster rates. For each compound, provide the contributing resonance forms for the carbocation intermediate that would be formed. Explain why the resonance forms provide information about the rate differences. Br 618 oted Br II OCH3 VI Br ofis 8 lo mubage AMA H er niese of lbeqe uoy bluow euleot edW8 Snollose gaiwollot eri ot Br oubog toa (blsitmwob) blell wol te anolog ollamots Aylno ed bluow enerT A Jelduch.a.ed.bluownodhaa.ailsnad a no anotog on tot lepie erT 8 Jolght s od bluow anoioig tom sr ot lenpie erTO olduob s ed bluow and aneporbyd S yino 1ot alsgatni bhow enotong lydlem arl hol lannie erf

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Question

9. The four compounds listed below undergo SN1 reactions at increasingly faster rates. For
each compound, provide the contributing resonance forms for the carbocation intermediate
that would be formed. Explain why the resonance forms provide information about the rate
differences.
Br
eloo
esnsib
to0 018-terl (V-) woled bew
Br
TII
ỌCH3
VI
Br
efin 8 to muloage AMA H ar ni ese of oaqe uoy bluow 6uleot iedW 8
Snoltone gaiwollot erl of
18
Br
oubog toom)
(blsitrwob) blall wol ta anoloiq olemots yino ed bluow enerfT A
Jolduch.a.ed.bluow.nodhsa.ailysad ad no anotong onl tot leipie enT 8
Jolght s od bluaw anoioiq lytom er tot lenpie erdT
Jolduob s ed bluow anoto
anegotbyd S yino not olsigatni bhiow anolong lydlam arl hol langiae enT3

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